Aliases & Classifications for Neuropathy

MalaCards integrated aliases for Neuropathy:

Name: Neuropathy 12 15 39 17 71
Peripheral Neuropathy 12 71
Peripheral Neuropathies 15

Classifications:



External Ids:

Disease Ontology 12 DOID:870
NCIt 49 C4731
SNOMED-CT 67 386033004
ICD10 32 G62.9
UMLS 71 C0031117 C0442874

Summaries for Neuropathy

Disease Ontology : 12 A nervous system disease that is located in nerves or nerve cells.

MalaCards based summary : Neuropathy, also known as peripheral neuropathy, is related to neuropathy, hereditary, with liability to pressure palsies and neuropathy, hereditary sensory and autonomic, type iia, and has symptoms including seizures, tremor and back pain. An important gene associated with Neuropathy is DLX6-AS1 (DLX6 Antisense RNA 1), and among its related pathways/superpathways is Neural Crest Differentiation. The drugs Aztreonam and Pravastatin have been mentioned in the context of this disorder. Affiliated tissues include nerves, breast and testes, and related phenotypes are behavior/neurological and cellular

Related Diseases for Neuropathy

Diseases in the Neuropathy family:

Autoimmune Neuropathy Hereditary Neuropathies

Diseases related to Neuropathy via text searches within MalaCards or GeneCards Suite gene sharing:

(showing 2735, show less)
# Related Disease Score Top Affiliating Genes
1 neuropathy, hereditary, with liability to pressure palsies 35.2 SPTLC2 PMP22 MPZ MFN2 GJB1 GDAP1
2 neuropathy, hereditary sensory and autonomic, type iia 35.1 WNK1 SPTLC2 SPTLC1 SLC12A6 NGF KIF1A
3 neuropathy, hereditary sensory and autonomic, type v 35.1 WNK1 SPTLC1 NGF KIF1A
4 hypertrophic neuropathy of dejerine-sottas 35.0 PMP22 MPZ MFN2 GJB1 GDAP1
5 neuropathy, congenital hypomyelinating, 1, autosomal recessive 35.0 SPTLC2 SLC12A6 PMP22 MPZ MFN2 GJB1
6 neuropathy, hereditary sensory, type ie 35.0 SPTLC2 SPTLC1 DNMT1
7 hereditary sensory neuropathy 35.0 WNK1 SPTLC2 SPTLC1 NGF MPZ KIF1A
8 hereditary sensory and autonomic neuropathy type 1 35.0 SPTLC2 SPTLC1 DNMT1
9 hereditary motor and sensory neuropathy, type iic 34.9 MPZ MFN2 GJB1 GDAP1
10 neuropathy, hereditary sensory and autonomic, type i, with cough and gastroesophageal reflux 34.9 SPTLC2 SPTLC1
11 diabetic neuropathy 34.9 PMP22 NGF MPZ
12 neuropathy, hereditary sensory and autonomic, type ia 34.9 WNK1 SPTLC2 SPTLC1
13 hereditary neuropathies 34.9 PMP22 MPZ MFN2 GJB1
14 deafness, x-linked 5, with peripheral neuropathy 34.8 DIAPH3 AIFM1
15 autonomic neuropathy 34.8 WNK1 SPTLC2 SPTLC1 SCN11A NGF KIF1A
16 sensory peripheral neuropathy 34.8 SPTLC1 SLC12A6 POLG PMP22 NGF MPZ
17 neuropathy, hereditary sensory and autonomic, type ic 34.8 SPTLC2 SPTLC1
18 agenesis of the corpus callosum with peripheral neuropathy 34.7 WNK1 SLC12A6
19 motor peripheral neuropathy 34.6 SLC12A6 POLG PMP22 MFN2 KIF1A GJB1
20 autoimmune peripheral neuropathy 34.5 MPZ GJB1
21 charcot-marie-tooth disease, x-linked dominant, 1 34.5 SPTLC1 PMP22 MPZ MFN2 GJB1 GDAP1
22 charcot-marie-tooth disease, axonal, type 2e 34.5 SPTLC1 SLC12A6 PMP22 NGF MPZ MFN2
23 neuropathy, hereditary sensory and autonomic, type iib 34.4 WNK1 KIF1A
24 charcot-marie-tooth disease, demyelinating, type 1b 34.4 PMP22 MPZ MFN2 GJB1 GDAP1
25 charcot-marie-tooth disease, demyelinating, type 1a 34.4 PMP22 MPZ MFN2 GJB1 GDAP1
26 charcot-marie-tooth disease, axonal, type 2b 34.4 SPTLC1 MPZ GJB1 GDAP1
27 charcot-marie-tooth disease, type 4d 34.4 MPZ GJB1 GDAP1
28 peripheral demyelinating neuropathy, central dysmyelination, waardenburg syndrome, and hirschsprung disease 34.4 MPZ GJB1
29 charcot-marie-tooth disease, demyelinating, type 1c 34.3 PMP22 MPZ GJB1 GDAP1
30 axonal neuropathy 34.3 POLG PMP22 MFN2 GDAP1 GAN AIFM1
31 peripheral nervous system disease 34.3 SPTLC1 SLC12A6 SCN11A POLG PMP22 NGF
32 charcot-marie-tooth disease, axonal, type 2a1 34.3 MPZ MFN2 GDAP1
33 charcot-marie-tooth disease, demyelinating, type 1d 34.3 PMP22 MPZ GJB1 GDAP1
34 charcot-marie-tooth disease/hereditary motor and sensory neuropathy 34.3 SPTLC2 SPTLC1 SLC12A6 PMP22 MPZ MFN2
35 asymmetric motor neuropathy 34.3 PMP22 MFN2 GAN
36 charcot-marie-tooth disease and deafness 34.3 SPTLC2 SPTLC1 PMP22 MPZ MFN2 KIF1A
37 charcot-marie-tooth disease, type 4a 34.2 MPZ MFN2 GJB1 GDAP1
38 optic nerve disease 34.2 POLG NGF MT-ND4 MFN2 GDAP1
39 charcot-marie-tooth disease, demyelinating, type 1f 34.2 MPZ GJB1 GDAP1
40 charcot-marie-tooth disease, axonal, type 2t 34.2 SLC12A6 GDAP1 GAN
41 charcot-marie-tooth disease, dominant intermediate b 34.2 MPZ GJB1 GDAP1
42 charcot-marie-tooth disease, type 4c 34.2 MPZ GJB1 GDAP1
43 charcot-marie-tooth disease, axonal, type 2f 34.2 MPZ MFN2 GJB1 GDAP1
44 charcot-marie-tooth disease, type 4b2 34.2 MPZ GJB1 GDAP1
45 charcot-marie-tooth disease, dominant intermediate a 34.2 MPZ GJB1 GDAP1
46 charcot-marie-tooth disease, axonal, type 2d 34.2 MPZ MFN2 GJB1 GDAP1
47 charcot-marie-tooth disease, axonal, type 2b2 34.2 MPZ MFN2 GDAP1
48 charcot-marie-tooth disease, axonal, type 2i 34.1 MPZ GJB1 GDAP1
49 charcot-marie-tooth disease, axonal, type 2l 34.1 MPZ MFN2 GDAP1
50 charcot-marie-tooth disease, x-linked recessive, 2 34.1 MPZ MFN2 GJB1
51 charcot-marie-tooth disease 34.1 WNK1 SPTLC2 SPTLC1 SLC12A6 SCN11A POLG
52 charcot-marie-tooth disease, demyelinating, type 4f 34.0 MPZ GJB1 GDAP1
53 autoimmune neuropathy 34.0 PMP22 MPZ
54 charcot-marie-tooth disease, axonal, type 2p 34.0 SLC12A6 GDAP1
55 charcot-marie-tooth disease, axonal, type 2r 34.0 SLC12A6 GDAP1
56 charcot-marie-tooth disease, dominant intermediate c 34.0 SPTLC1 MPZ GJB1 GDAP1
57 charcot-marie-tooth disease, axonal, type 2j 34.0 MPZ GDAP1
58 charcot-marie-tooth disease, axonal, type 2w 34.0 MPZ MFN2 GJB1 GDAP1
59 charcot-marie-tooth disease, type 4b3 34.0 PMP22 MPZ GDAP1
60 charcot-marie-tooth disease, axonal, type 2k 34.0 KIF1A GDAP1
61 charcot-marie-tooth disease, recessive intermediate a 34.0 MFN2 GDAP1
62 charcot-marie-tooth disease, dominant intermediate e 33.9 MPZ GDAP1
63 charcot-marie-tooth disease, axonal, type 2b1 33.9 MFN2 GDAP1
64 nerve compression syndrome 33.8 PMP22 NGF MPZ
65 roussy-levy hereditary areflexic dystasia 33.8 PMP22 MPZ
66 brachial plexus neuropathy 33.8 PMP22 MPZ
67 polyneuropathy 33.5 POLG PMP22 NGF MPZ MFN2 GJB1
68 mononeuropathy 33.5 PMP22 NGF MPZ
69 3-methylglutaconic aciduria, type iii 33.3 POLG MT-ND4 MFN2 GJB1 GDAP1
70 charcot-marie-tooth disease x-linked recessive 4 33.2 MPZ GJB1 AIFM1
71 foot drop 33.0 PMP22 MPZ
72 neuromuscular disease 32.9 PMP22 MPZ MFN2 GJB1 GDAP1 GAN
73 charcot-marie-tooth disease intermediate type 32.9 MPZ MFN2 GJB1 GDAP1
74 argyll robertson pupil 32.7 MPZ GDAP1
75 cranial nerve disease 32.7 POLG MT-ND4 MFN2
76 ataxia-oculomotor apraxia 3 32.3 SLC12A6 GAN
77 tooth disease 32.2 SPTLC1 PMP22 MPZ MFN2 GJB1 GDAP1
78 neuritis 32.1 PMP22 MT-ND4 MPZ
79 motor neuron disease 31.9 SCN11A MPZ MFN2 AIFM1
80 amyotrophic neuralgia 31.3 PMP22 MPZ
81 chronic polyneuropathy 31.2 PMP22 GJB1
82 neurogenic arthropathy 31.0 SPTLC1 NGF
83 pupil disease 30.2 MPZ GDAP1
84 trigeminal nerve disease 29.8 SCN11A NGF
85 pearson marrow-pancreas syndrome 29.4 POLG MT-ND4
86 neuromyotonia and axonal neuropathy, autosomal recessive 12.6
87 neuropathy, hereditary motor and sensory, type via, with optic atrophy 12.6
88 nonarteritic anterior ischemic optic neuropathy 12.6
89 neuropathy, hereditary sensory and autonomic, type vii 12.6
90 neuropathy, hereditary motor and sensory, russe type 12.5
91 neuropathy, hereditary sensory and autonomic, type vi 12.5
92 neuropathy, hereditary motor and sensory, okinawa type 12.5
93 giant axonal neuropathy 1, autosomal recessive 12.5
94 giant axonal neuropathy 12.5
95 sensory ataxic neuropathy, dysarthria, and ophthalmoparesis 12.5
96 hereditary motor and sensory neuropathy v 12.5
97 neuropathy, ataxia, and retinitis pigmentosa 12.5
98 congenital cataracts, facial dysmorphism, and neuropathy 12.5
99 spinocerebellar ataxia type 1 with axonal neuropathy 12.5
100 auditory neuropathy, autosomal dominant, 1 12.5
101 peripheral neuropathy, myopathy, hoarseness, and hearing loss 12.5
102 neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive 12.5
103 spastic paraplegia, optic atrophy, and neuropathy 12.5
104 spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1 12.4
105 neuropathy, hereditary sensory and autonomic, type iii 12.4
106 giant axonal neuropathy 2, autosomal dominant 12.4
107 neuropathy, hereditary motor and sensory, type vib, with optic atrophy 12.4
108 cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome 12.4
109 neuropathy, hereditary sensory, type id 12.4
110 multifocal motor neuropathy 12.4
111 leukoencephalopathy with dystonia and motor neuropathy 12.4
112 auditory neuropathy spectrum disorder 12.4
113 neuropathy, hereditary, with or without age-related macular degeneration 12.4
114 ataxia neuropathy spectrum 12.4
115 neuropathy, hereditary sensory, type if 12.4
116 mental retardation, enteropathy, deafness, peripheral neuropathy, ichthyosis, and keratoderma 12.4
117 cerebellar ataxia, neuropathy, and vestibular areflexia syndrome 12.4
118 sptlc1-related hereditary sensory neuropathy 12.4
119 spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2 12.4
120 cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia 12.4
121 ulnar neuropathy 12.4
122 neuropathy, hereditary sensory, type iic 12.4
123 neuropathy, congenital hypomyelinating, 2 12.4
124 neurodevelopmental disorder with hypotonia, neuropathy, and deafness 12.3
125 peripheral neuropathy, autosomal recessive, with or without impaired intellectual development 12.3
126 spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3 12.3
127 46,xy gonadal dysgenesis, partial, with minifascicular neuropathy 12.3
128 neuropathy, hereditary sensory and autonomic, type viii 12.3
129 neuropathy, congenital hypomyelinating, 3 12.3
130 distal hereditary motor neuropathies 12.3
131 auditory neuropathy and optic atrophy 12.3
132 hypertrichosis, congenital anterior cervical, with peripheral sensory and motor neuropathy 12.3
133 radial neuropathy 12.3
134 deafness, nerve type, with mesenteric diverticula of small bowel and progressive sensory neuropathy 12.3
135 optic atrophy 7 with or without auditory neuropathy 12.3
136 neuropathy, hereditary motor and sensory, type vic, with optic atrophy 12.3
137 arteritic anterior ischemic optic neuropathy 12.3
138 insensitivity to pain, congenital, with anhidrosis 12.3
139 acute motor axonal neuropathy 12.3
140 neuropathy, hereditary sensory, x-linked 12.3
141 autonomic peripheral neuropathy 12.2
142 neuropathy, hereditary sensory, atypical 12.2
143 diabetic autonomic neuropathy 12.2
144 localized hypertrophic neuropathy 12.2
145 chronic relapsing inflammatory optic neuropathy 12.2
146 polyglucosan body neuropathy, adult form 12.2
147 neuropathy, hereditary motor and sensory, with deafness, mental retardation, and absent sensory large myelinated fibers 12.2
148 neuropathy, hereditary thermosensitive 12.2
149 sorbitol dehydrogenase deficiency with peripheral neuropathy 12.2
150 femoral neuropathy 12.2
151 autosomal recessive axonal hereditary motor and sensory neuropathy 12.2
152 alcoholic neuropathy 12.2
153 optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy 12.2
154 sciatic neuropathy 12.2
155 hereditary optic neuropathy 12.2
156 refsum disease, classic 12.1
157 tibial neuropathy 12.1
158 charcot-marie-tooth hereditary neuropathy 12.1
159 amyloid neuropathy 12.1
160 peroneal neuropathy 12.1
161 ischemic neuropathy 12.1
162 toxic optic neuropathy 12.1
163 visceral neuropathy, familial, autosomal dominant 12.1
164 leber optic atrophy 12.1
165 keratoderma, palmoplantar, with nail dystrophy and hereditary motor-sensory neuropathy 12.1
166 spastic paraplegia with neuropathy and poikiloderma 12.1
167 ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia 12.1
168 hereditary sensorimotor neuropathy with hyperelastic skin 12.1
169 cerebellar ataxia with peripheral neuropathy 12.1
170 hereditary motor and sensory neuropathy with acrodystrophy 12.1
171 uremic neuropathy 12.1
172 median neuropathy 12.1
173 charcot-marie-tooth disease, axonal, autosomal dominant, type 2a2a 12.1
174 charcot-marie-tooth disease, x-linked recessive, 4, with or without cerebellar ataxia 12.1
175 nutritional optic neuropathy 12.1
176 idiopathic peripheral autonomic neuropathy 12.1
177 leber hereditary optic neuropathy with demyelinating disease of cns 12.1
178 neuropathy, congenital, with arthrogryposis multiplex 12.1
179 motor neuropathy, peripheral, with dysautonomia 12.1
180 amyloidosis, hereditary, transthyretin-related 12.1
181 charcot-marie-tooth disease, x-linked recessive, 5 12.1
182 hereditary sensory and autonomic neuropathy with deafness and global delay 12.1
183 charcot-marie-tooth disease, axonal, type 2q 12.1
184 charcot-marie-tooth disease, type 4k 12.1
185 neuropathy, painful 12.0
186 hereditary motor and sensory neuropathy with agenesis of the corpus callosum 12.0
187 gdap1-related hereditary motor and sensory neuropathy 12.0
188 mfn2 hereditary motor and sensory neuropathy 12.0
189 charcot-marie-tooth neuropathy x type 5 12.0
190 autosomal recessive distal hereditary motor neuropathy 12.0
191 sodium channelopathy-related small fiber neuropathy 12.0
192 giant axonal neuropathy 2 12.0
193 severe infantile axonal neuropathy 12.0
194 charcot-marie-tooth disease, type 4b1 12.0
195 charcot-marie-tooth disease, axonal, type 2n 12.0
196 charcot-marie-tooth disease, type 4h 12.0
197 erythermalgia, primary 12.0
198 charcot-marie-tooth disease, axonal, type 2o 12.0
199 amyotrophy, hereditary neuralgic 12.0
200 charcot-marie-tooth disease, axonal, type 2v 12.0
201 neuronopathy, distal hereditary motor, type va 12.0
202 acute motor and sensory axonal neuropathy 12.0
203 spastic paraplegia-optic atrophy-neuropathy and spastic paraplegia-optic atrophy-neuropathy-related disorder 12.0
204 neuropathy with hearing impairment 12.0
205 autosomal dominant hereditary demyelinating motor and sensory neuropathy 12.0
206 autosomal dominant hereditary sensory and autonomic neuropathy 12.0
207 autosomal recessive hereditary sensory and autonomic neuropathy 12.0
208 autosomal dominant hereditary axonal motor and sensory neuropathy 12.0
209 autosomal recessive hereditary demyelinating motor and sensory neuropathy 12.0
210 leber optic atrophy and dystonia 12.0
211 gjb1 disorders: charcot marie tooth neuropathy and central nervous system phenotypes 12.0
212 gars1-associated axonal neuropathy 12.0
213 charcot-marie-tooth disease, axonal, type 2u 12.0
214 acute sensory ataxic neuropathy 12.0
215 acquired peripheral neuropathy 12.0
216 peripheral neuropathy associated with monoclonal gammopathy 12.0
217 charcot-marie-tooth disease, x-linked dominant, 6 12.0
218 optic atrophy, hearing loss, and peripheral neuropathy, autosomal recessive 12.0
219 rare peripheral neuropathy 12.0
220 charcot-marie-tooth disease, recessive intermediate c 12.0
221 x-linked distal hereditary motor neuropathy 12.0
222 demyelinating hereditary motor and sensory neuropathy 12.0
223 axonal hereditary motor and sensory neuropathy 12.0
224 neuropathy, hereditary motor and sensory, with excessive myelin folding complex, autosomal recessive 12.0
225 peripheral neuropathy, ataxia, focal necrotizing encephalopathy, and spongy degeneration of brain 12.0
226 infantile axonal neuropathy 12.0
227 distal hereditary motor neuropathy type 7 12.0
228 neuropathy, hereditary sensorimotor, with upper motor neuron, visual pathway and autonomic disturbance 12.0
229 neuropathy, with paraprotein in serum, cerebrospinal fluid and urine 12.0
230 optic atrophy, hearing loss, and peripheral neuropathy, autosomal dominant 12.0
231 spinocerebellar ataxia with rigidity and peripheral neuropathy 12.0
232 hypertrophic neuropathy and cataract 12.0
233 visceral neuropathy, familial, autosomal recessive 12.0
234 laryngeal abductor paralysis with cerebellar ataxia and motor neuropathy 12.0
235 neuropathy, hereditary sensory and autonomic, adult-onset, with anosmia 12.0
236 syndromic hereditary optic neuropathy 12.0
237 congenital axonal neuropathy with encephalopathy 12.0
238 charcot-marie-tooth disease, recessive intermediate b 12.0
239 carpal tunnel syndrome 12.0
240 x-linked charcot-marie-tooth disease 11.9
241 mitochondrial dna depletion syndrome 7 11.9
242 moebius axonal neuropathy hypogonadism 11.9
243 x-linked hereditary sensory and autonomic neuropathy with deafness 11.9
244 mitochondrial trifunctional protein deficiency 11.9
245 mitochondrial dna depletion syndrome 6 11.9
246 deafness, autosomal recessive 9 11.9
247 charcot-marie-tooth disease, x-linked recessive, 3 11.9
248 charcot-marie-tooth disease, dominant intermediate d 11.9
249 distal hereditary motor neuronopathy type 2 11.9
250 inflammatory and toxic neuropathy 11.9
251 glossopharyngeal motor neuropathy 11.9
252 infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome 11.9
253 microcephaly-complex motor and sensory axonal neuropathy syndrome 11.9
254 neuronopathy, distal hereditary motor, type iib 11.9
255 charcot-marie-tooth disease, axonal, type 2x 11.9
256 charcot-marie-tooth disease, axonal, type 2dd 11.9
257 tangier disease 11.9
258 charcot-marie-tooth disease, axonal, type 2ee 11.9
259 charcot-marie-tooth disease, axonal, type 2z 11.9
260 charcot-marie-tooth disease, axonal, type 2cc 11.9
261 spinocerebellar ataxia 18 11.9
262 deafness, sensorineural, with peripheral neuropathy and arterial disease 11.9
263 chronic demyelinizing neuropathy with igm monoclonal 11.9
264 deafness mesenteric diverticula of small bowel neuropathy 11.9
265 deafness peripheral neuropathy arterial disease 11.9
266 visceral neuropathy familial 11.9
267 autosomal dominant optic atrophy and peripheral neuropathy 11.9
268 moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome 11.9
269 hypomyelination neuropathy-arthrogryposis syndrome 11.9
270 infectious disease with peripheral neuropathy 11.9
271 malignant lymphoma with peripheral neuropathy 11.9
272 rare hereditary systemic disease with peripheral neuropathy 11.9
273 rare hereditary metabolic disease with peripheral neuropathy 11.9
274 rare hereditary neurologic disease with peripheral neuropathy 11.9
275 rare hereditary disease with peripheral neuropathy 11.9
276 systemic inflammatory disease associated with an acquired peripheral neuropathy 11.9
277 hematological disease associated with an acquired peripheral neuropathy 11.9
278 acquired amyloid peripheral neuropathy 11.9
279 solid tumor associated with an acquired peripheral neuropathy 11.9
280 mitochondrial disease with peripheral neuropathy 11.9
281 acute pure sensory neuropathy 11.9
282 laminopathy with peripheral neuropathy 11.9
283 periodic paralysis with later-onset distal motor neuropathy 11.9
284 non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy 11.9
285 autoimmune/inflammatory optic neuropathy 11.9
286 autosomal dominant distal axonal motor neuropathy-myofibrillar myopathy syndrome 11.9
287 visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome 11.9
288 optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome 11.9
289 genetic peripheral neuropathy 11.9
290 guillain-barre syndrome 11.9
291 neuronopathy, distal hereditary motor, type iia 11.8
292 neuronopathy, distal hereditary motor, type viia 11.8
293 charcot-marie-tooth disease, demyelinating, type 1g 11.8
294 lewis-sumner syndrome 11.8
295 spastic paraplegia 49, autosomal recessive 11.8
296 neuronopathy, distal hereditary motor, type i 11.8
297 neuronopathy, distal hereditary motor, type iic 11.8
298 abetalipoproteinemia 11.8
299 amyloidosis, finnish type 11.8
300 canomad syndrome 11.8
301 spinocerebellar ataxia 4 11.7
302 spinocerebellar ataxia, autosomal recessive 21 11.7
303 encephalopathy due to defective mitochondrial and peroxisomal fission 2 11.7
304 microvascular complications of diabetes 1 11.7
305 long-chain 3-hydroxyacyl-coa dehydrogenase deficiency 11.7
306 charcot-marie-tooth disease type 2a2b 11.7
307 neuronopathy, distal hereditary motor, type viib 11.7
308 blau syndrome 11.7
309 charcot-marie-tooth disease, axonal, with vocal cord paresis, autosomal recessive 11.7
310 spastic ataxia 5, autosomal recessive 11.7
311 spastic paraplegia 10, autosomal dominant 11.7
312 deafness, autosomal recessive 59 11.7
313 adult polyglucosan body disease 11.7
314 spinal muscular atrophy, distal, autosomal recessive, 2 11.7
315 spinal muscular atrophy, distal, autosomal recessive, 1 11.7
316 neuronopathy, distal hereditary motor, type iid 11.6
317 tarsal tunnel syndrome 11.6
318 polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract 11.6
319 charcot-marie-tooth disease, type 4j 11.6
320 spastic paraplegia 9a, autosomal dominant 11.6
321 charcot-marie-tooth disease, axonal, type 2h 11.6
322 spastic ataxia, charlevoix-saguenay type 11.5
323 demyelinating polyneuropathy 11.5
324 indifference to pain, congenital, autosomal recessive 11.5
325 harel-yoon syndrome 11.5
326 lattice corneal dystrophy type ii 11.5
327 mononeuritis multiplex 11.5
328 neuronopathy, distal hereditary motor, type viii 11.5
329 spinal muscular atrophy, distal, x-linked 3 11.5
330 neuronopathy, distal hereditary motor, type vb 11.5
331 myasthenic syndrome, congenital, 7, presynaptic 11.5
332 neuronopathy, distal hereditary motor, type ix 11.5
333 charcot-marie-tooth disease, dominant intermediate f 11.4
334 mitochondrial dna depletion syndrome 4b 11.4
335 laurence-moon syndrome 11.4
336 alpha-methylacyl-coa racemase deficiency 11.4
337 intestinal pseudo-obstruction 11.4
338 machado-joseph disease 11.4
339 autosomal dominant charcot-marie-tooth disease type 2 with giant axons 11.4
340 marinesco-sjogren syndrome 11.4
341 chediak-higashi syndrome 11.4
342 spastic paraplegia 7, autosomal recessive 11.4
343 charcot-marie-tooth disease, recessive intermediate d 11.4
344 systemic lupus erythematosus 11.4
345 charcot-marie-tooth disease, axonal, autosomal recessive, type 2a2b 11.4
346 autosomal dominant distal hereditary motor neuronopathy 11.4
347 spinocerebellar ataxia 2 11.4
348 spinocerebellar ataxia 25 11.4
349 ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus 11.4
350 spinocerebellar ataxia 1 11.4
351 chronic progressive external ophthalmoplegia 11.4
352 erythromelalgia 11.4
353 chronic inflammatory demyelinating polyradiculoneuropathy 11.4
354 charcot-marie-tooth disease type 2a2a 11.4
355 waldenstroem's macroglobulinemia 11.3
356 radiculopathy 11.3
357 spastic paraplegia 15 11.3
358 autonomic dysfunction 11.3
359 hereditary spastic paraplegia 11.3
360 piriformis syndrome 11.3
361 guillain-barre syndrome, familial 11.3
362 spinal muscular atrophy, type i 11.3
363 myopathy 11.3
364 spastic paraplegia 39, autosomal recessive 11.3
365 spinocerebellar ataxia 46 11.3
366 leigh syndrome 11.3
367 syncope 11.3
368 pure autonomic failure 11.3
369 leprosy 3 11.3
370 microvascular complications of diabetes 5 11.3
371 progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 1 11.3
372 cerebrotendinous xanthomatosis 11.3
373 pnpla6-related disorders 11.3
374 spastic paraplegia 3a 11.3
375 lipomatosis, multiple symmetric 11.3
376 paroxysmal extreme pain disorder 11.3
377 achalasia-addisonianism-alacrima syndrome 11.3
378 neuronal intranuclear inclusion disease 11.3
379 myoclonic epilepsy associated with ragged-red fibers 11.3
380 myofibrillar myopathy 11.3
381 fainting 11.3
382 spastic paraplegia 23, autosomal recessive 11.2
383 dysautonomia 11.2
384 mitochondrial dna depletion syndrome 4a 11.2
385 mannosidosis, beta a, lysosomal 11.2
386 progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 1 11.2
387 oliver-mcfarlane syndrome 11.2
388 mohr-tranebjaerg syndrome 11.2
389 wolfram syndrome 2 11.2
390 progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 3 11.2
391 neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 11.2
392 muscular dystrophy, limb-girdle, autosomal recessive 23 11.2
393 neurodevelopmental disorder with central and peripheral motor dysfunction 11.2
394 siddiqi syndrome 11.2
395 familial episodic pain syndrome 11.2
396 ataxia with vitamin e deficiency 11.2
397 mitochondrial membrane protein-associated neurodegeneration 11.2
398 spastic paraplegia 11 11.2
399 diabetes mellitus, type i 11.2
400 diabetes mellitus, noninsulin-dependent 11.2
401 prp systemic amyloidosis 11.2
402 autoimmune autonomic ganglionopathy 11.2
403 ntrk1 congenital insensitivity to pain with anhidrosis 11.2
404 microvascular complications of diabetes 3 11.2
405 microvascular complications of diabetes 4 11.2
406 microvascular complications of diabetes 6 11.2
407 microvascular complications of diabetes 7 11.2
408 beriberi 11.2
409 acute pandysautonomia 11.2
410 alcohol use disorder 11.2
411 optic atrophy 1 11.2
412 charcot-marie-tooth disease type 2a 11.2
413 spastic paraplegia 17, autosomal dominant 11.2
414 porphyria, acute intermittent 11.2
415 polyradiculopathy 11.2
416 hereditary amyloidosis 11.2
417 fabry disease 11.2
418 spinal muscular atrophy, distal, autosomal recessive, 5 11.2
419 lattice corneal dystrophy 11.2
420 retinitis pigmentosa 11.2
421 visceral myopathy 11.2
422 boylan dew greco syndrome 11.2
423 familial amyloidosis, finnish type 11.2
424 paraneoplastic syndromes 11.2
425 microvascular complications of diabetes 2 11.1
426 antiphospholipid syndrome 11.1
427 spinocerebellar degeneration 11.1
428 krabbe disease 11.1
429 optic atrophy 3, autosomal dominant 11.1
430 metachromatic leukodystrophy 11.1
431 intermittent claudication 11.1
432 leber plus disease 11.1
433 wolfram syndrome 11.1
434 parsonage turner syndrome 11.1
435 mitochondrial neurogastrointestinal encephalomyopathy 11.1
436 mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes 11.1
437 glaucoma, normal tension 11.1
438 centronuclear myopathy 11.1
439 acute porphyria 11.1
440 brachial plexus lesion 11.1
441 mitochondrial complex i deficiency, nuclear type 1 11.1
442 spastic paraplegia 3, autosomal dominant 11.1
443 progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 2 11.1
444 progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 4 11.1
445 moebius syndrome 11.1
446 ataxia-telangiectasia 11.1
447 mitochondrial complex iv deficiency 11.1
448 arts syndrome 11.1
449 spastic ataxia 11.1
450 abducens nerve disease 11.1
451 olivopontocerebellar atrophy 11.1
452 episodic ataxia 11.1
453 variegate porphyria 11.1
454 smith-magenis syndrome 11.1
455 spastic paraplegia 55, autosomal recessive 11.1
456 osteopetrosis 11.1
457 nuclear gene-encoded leigh syndrome 11.1
458 spastic paraplegia 10 11.1
459 epilepsy, progressive myoclonic, 4, with or without renal failure 11.1
460 cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss 11.1
461 spastic paraplegia 31, autosomal dominant 11.1
462 mononeuropathy of the median nerve, mild 11.1
463 optic atrophy 10 with or without ataxia, mental retardation, and seizures 11.1
464 charcot-marie-tooth disease, dominant intermediate g 11.1
465 fragile x-associated tremor/ataxia syndrome 11.1
466 notalgia paresthetica 11.1
467 oculopharyngeal muscular dystrophy 11.1
468 exfoliation syndrome 11.1
469 deafness and myopia 11.1
470 mcleod syndrome 11.1
471 spastic paraplegia 30, autosomal dominant 11.1
472 myopathy, myofibrillar, 6 11.1
473 neurodegeneration with brain iron accumulation 4 11.1
474 perrault syndrome 11.1
475 niemann-pick disease 11.1
476 coproporphyria, hereditary 11.1
477 glaucoma 1, open angle, a 11.1
478 ataxia-pancytopenia syndrome 11.1
479 behr syndrome 11.1
480 cerebellar ataxia, early-onset, with retained tendon reflexes 11.1
481 spastic paraplegia 15, autosomal recessive 11.1
482 vitamin e, familial isolated deficiency of 11.1
483 mitochondrial complex i deficiency, nuclear type 12 11.1
484 mitochondrial complex i deficiency, mitochondrial type 1 11.1
485 spinocerebellar ataxia 10 11.1
486 spinocerebellar ataxia, autosomal recessive 4 11.1
487 posterior column ataxia with retinitis pigmentosa 11.1
488 microcephaly, seizures, and developmental delay 11.1
489 nescav syndrome 11.1
490 wolfram-like syndrome, autosomal dominant 11.1
491 spinocerebellar ataxia 43 11.1
492 neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures 11.1
493 cerebellar ataxia type 43 11.1
494 autonomic nervous system disease 11.1
495 tyrosinemia 11.1
496 autoimmune gastrointestinal dysmotility 11.1
497 paraneoplastic neurologic disorders 11.1
498 spastic paraplegia 14 11.1
499 spastic paraplegia type 49 11.1
500 amyotrophic lateral sclerosis 4, juvenile 11.1
501 spinal muscular atrophy, distal, autosomal recessive, 3 11.1
502 congenital disorder of glycosylation, type ia 11.1
503 cerebellar ataxia, deafness, and narcolepsy, autosomal dominant 11.1
504 mitochondrial dna depletion syndrome 1 11.0
505 spinocerebellar ataxia 11 11.0
506 spastic paraplegia 56, autosomal recessive 11.0
507 charcot-marie-tooth disease type 1g 11.0
508 arnold stickler bourne syndrome 11.0
509 polyneuropathy associated with igm monoclonal gammapathy with anti-mag 11.0
510 choreoacanthocytosis 10.9
511 ribose 5-phosphate isomerase deficiency 10.9
512 spastic paraplegia 26, autosomal recessive 10.9
513 spinocerebellar ataxia 23 10.9
514 leukodystrophy, hypomyelinating, 5 10.9
515 mitochondrial dna depletion syndrome 8a 10.9
516 perrault syndrome 3 10.9
517 mental retardation, autosomal dominant 13 10.9
518 myopathy with extrapyramidal signs 10.9
519 spinocerebellar ataxia, autosomal recessive 16 10.9
520 ataxia-oculomotor apraxia 4 10.9
521 spastic paraplegia 74, autosomal recessive 10.9
522 yuan-harel-lupski syndrome 10.9
523 neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features 10.9
524 mitochondrial complex v deficiency, nuclear type 5 10.9
525 epileptic encephalopathy, early infantile, 81 10.9
526 arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum 10.9
527 mitochondrial dna depletion syndrome 10.9
528 lupus - neurological sequelae 10.9
529 familial syringomyelia 10.9
530 slowed nerve conduction velocity, autosomal dominant 10.9
531 charcot-marie-tooth disease type 5 10.8
532 radial nerve lesion 10.8
533 spinal muscular atrophy with respiratory distress type 2 10.8
534 genetic motor neuron disease 10.8 SCN11A MPZ MFN2
535 charcot-marie-tooth disease with ptosis and parkinsonism 10.8
536 mitochondrial complex iii deficiency, nuclear type 1 10.8
537 lateral meningocele syndrome 10.8
538 osteopetrosis, autosomal dominant 2 10.8
539 pruritus, hereditary localized 10.8
540 spinocerebellar ataxia, autosomal recessive 2 10.8
541 gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to 10.8
542 van buchem disease 10.8
543 chylomicron retention disease 10.8
544 metachromatic leukodystrophy due to saposin b deficiency 10.8
545 mitochondrial dna depletion syndrome 3 10.8
546 osteopetrosis, autosomal recessive 1 10.8
547 osteopetrosis, autosomal recessive 2 10.8
548 osteopetrosis, autosomal recessive 5 10.8
549 osteopetrosis, autosomal recessive 3 10.8
550 imerslund-grasbeck syndrome 1 10.8
551 intestinal pseudoobstruction, neuronal, chronic idiopathic, x-linked 10.8
552 combined oxidative phosphorylation deficiency 6 10.8
553 immunodeficiency 47 10.8
554 mitochondrial complex i deficiency, nuclear type 30 10.8
555 wieacker-wolff syndrome, female-restricted 10.8
556 mitochondrial complex v deficiency, mitochondrial type 1 10.8
557 phosphoglycerate dehydrogenase deficiency 10.8
558 mitochondrial complex v deficiency, nuclear type 1 10.8
559 spinocerebellar ataxia 19 10.8
560 osteopetrosis, autosomal dominant 1 10.8
561 combined oxidative phosphorylation deficiency 1 10.8
562 myopathy, myofibrillar, 3 10.8
563 kanzaki disease 10.8
564 tukel syndrome 10.8
565 myopathy, myofibrillar, 4 10.8
566 osteopetrosis, autosomal recessive 4 10.8
567 osteopetrosis, autosomal recessive 6 10.8
568 osteopetrosis, autosomal recessive 7 10.8
569 porphyria, acute hepatic 10.8
570 progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 5 10.8
571 spastic paraplegia 48, autosomal recessive 10.8
572 coenzyme q10 deficiency, primary, 2 10.8
573 mitochondrial pyruvate carrier deficiency 10.8
574 peroxisome biogenesis disorder 6b 10.8
575 peroxisome biogenesis disorder 8b 10.8
576 peroxisome biogenesis disorder 9b 10.8
577 spastic paraplegia 53, autosomal recessive 10.8
578 spastic paraplegia 54, autosomal recessive 10.8
579 mitochondrial complex iii deficiency, nuclear type 2 10.8
580 congenital disorder of deglycosylation 10.8
581 spastic paraplegia 79, autosomal recessive 10.8
582 hypobetalipoproteinemia, familial, 1 10.8
583 neurodegeneration with brain iron accumulation 6 10.8
584 spastic paraplegia 57, autosomal recessive 10.8
585 spastic paraplegia 61, autosomal recessive 10.8
586 vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome 10.8
587 pontocerebellar hypoplasia, type 10 10.8
588 combined oxidative phosphorylation deficiency 24 10.8
589 coenzyme q10 deficiency, primary, 8 10.8
590 combined oxidative phosphorylation deficiency 29 10.8
591 spinocerebellar ataxia, autosomal recessive 26 10.8
592 leukodystrophy, progressive, early childhood-onset 10.8
593 mitochondrial complex i deficiency, nuclear type 2 10.8
594 mitochondrial complex i deficiency, nuclear type 4 10.8
595 mitochondrial complex i deficiency, nuclear type 6 10.8
596 mitochondrial complex i deficiency, nuclear type 7 10.8
597 mitochondrial complex i deficiency, nuclear type 8 10.8
598 mitochondrial complex i deficiency, nuclear type 9 10.8
599 mitochondrial complex i deficiency, nuclear type 10 10.8
600 mitochondrial complex i deficiency, nuclear type 11 10.8
601 mitochondrial complex i deficiency, nuclear type 13 10.8
602 mitochondrial complex i deficiency, nuclear type 14 10.8
603 mitochondrial complex i deficiency, nuclear type 15 10.8
604 mitochondrial complex i deficiency, nuclear type 16 10.8
605 mitochondrial complex i deficiency, nuclear type 17 10.8
606 mitochondrial complex i deficiency, nuclear type 18 10.8
607 mitochondrial complex i deficiency, nuclear type 19 10.8
608 mitochondrial complex i deficiency, nuclear type 21 10.8
609 mitochondrial complex i deficiency, nuclear type 22 10.8
610 mitochondrial complex i deficiency, nuclear type 23 10.8
611 mitochondrial complex i deficiency, nuclear type 24 10.8
612 mitochondrial complex i deficiency, nuclear type 25 10.8
613 mitochondrial complex i deficiency, nuclear type 26 10.8
614 mitochondrial complex i deficiency, nuclear type 27 10.8
615 mitochondrial complex i deficiency, nuclear type 28 10.8
616 mitochondrial complex i deficiency, nuclear type 29 10.8
617 mitochondrial complex i deficiency, nuclear type 31 10.8
618 mitochondrial complex i deficiency, nuclear type 32 10.8
619 mitochondrial complex i deficiency, nuclear type 33 10.8
620 leukodystrophy, hypomyelinating, 18 10.8
621 spastic ataxia 9, autosomal recessive 10.8
622 neuromuscular disease and ocular or auditory anomalies with or without seizures 10.8
623 mitochondrial complex i deficiency, nuclear type 34 10.8
624 congenital bile acid synthesis defect 10.8
625 spastic ataxia 1 10.8
626 spastic ataxia 2 10.8
627 muscular disease 10.8
628 46,xy sex reversal 10.8
629 chronic nk-cell lymphocytosis 10.8
630 spastic paraplegia 8 10.8
631 hamanishi ueba tsuji syndrome 10.8
632 late-onset distal myopathy, markesbery-griggs type 10.8
633 lipidosis with triglycerid storage disease 10.8
634 neonatal adrenoleukodystrophy 10.8
635 ramos arroyo clark syndrome 10.8
636 spastic paraplegia 19 10.8
637 spastic paraplegia 25 10.8
638 spastic paraplegia 26 10.8
639 spastic paraplegia 29 10.8
640 spastic paraplegia 3 10.8
641 spastic paraplegia 5a 10.8
642 spastic paraplegia 6 10.8
643 alg1-congenital disorder of glycosylation 10.8
644 aids - neurological complications 10.8
645 ataxias and cerebellar or spinocerebellar degeneration 10.8
646 familial spastic paralysis 10.8
647 spinocerebellar atrophy 10.8
648 ataxia and polyneuropathy, adult-onset 10.8
649 charcot-marie-tooth disease type x 10.7 SPTLC1 PMP22 MPZ MFN2 GJB1 GDAP1
650 abnormal pupillary function 10.7 MPZ GDAP1
651 vasculitis 10.7
652 mononeuritis of lower limb 10.7 PMP22 NGF
653 lesion of sciatic nerve 10.7 PMP22 NGF
654 combined oxidative phosphorylation deficiency 7 10.7 MT-ND4 MFN2
655 hyperglycemia 10.7
656 diabetes mellitus 10.6
657 yemenite deaf-blind hypopigmentation syndrome 10.6
658 optic neuritis 10.6
659 diabetic polyneuropathy 10.6
660 paresthesia 10.6
661 amyloidosis 10.6
662 facial onset sensory and motor neuronopathy 10.6
663 autosomal dominant charcot-marie-tooth disease type 2g 10.6
664 polyradiculoneuropathy 10.6
665 muscular atrophy 10.6
666 branchiootic syndrome 1 10.5
667 hansen's disease 10.5
668 myeloma, multiple 10.5
669 lateral sclerosis 10.5
670 amyotrophic lateral sclerosis 1 10.5
671 kearns-sayre syndrome 10.5
672 sensorineural hearing loss 10.5
673 vascular disease 10.5
674 impotence 10.5
675 chronic pain 10.5
676 paraplegia 10.5
677 hypoglycemia 10.4
678 encephalopathy 10.4
679 intraocular pressure quantitative trait locus 10.4
680 vitamin b12 deficiency 10.4
681 allergic hypersensitivity disease 10.4
682 tremor 10.4
683 cataract 10.4
684 alcohol dependence 10.4
685 anhidrosis 10.4
686 constipation 10.4
687 monoclonal gammopathy of uncertain significance 10.4
688 scotoma 10.4
689 plexopathy 10.4
690 peripheral vascular disease 10.4
691 wallerian degeneration 10.4
692 autoimmune disease 10.4
693 sarcoidosis 1 10.4
694 cryoglobulinemia 10.4
695 open-angle glaucoma 10.4
696 kidney disease 10.4
697 lymphoma 10.3
698 hypotonia 10.3
699 dysphagia 10.3
700 gastroparesis 10.3
701 lipid metabolism disorder 10.3
702 posttransplant acute limbic encephalitis 10.3
703 macroglobulinemia 10.3
704 respiratory failure 10.3
705 spinal muscular atrophy 10.3
706 eye disease 10.3
707 mitochondrial disorders 10.3
708 papilledema 10.3
709 exophthalmos 10.3
710 churg-strauss syndrome 10.3
711 immune deficiency disease 10.3
712 diarrhea 10.3
713 facial paralysis 10.3
714 dystonia 10.3
715 alpha/beta t-cell lymphopenia with gamma/delta t-cell expansion, severe cytomegalovirus infection, and autoimmunity 10.3
716 porphyria 10.3
717 hepatitis c 10.3
718 47,xyy 10.3
719 sleep apnea 10.3
720 poems syndrome 10.3
721 connective tissue disease 10.3
722 end stage renal disease 10.3
723 lupus erythematosus 10.3
724 autosomal recessive disease 10.3
725 miller fisher syndrome 10.3
726 arthropathy 10.3
727 glaucoma, primary open angle 10.3
728 pathologic nystagmus 10.3
729 allergic angiitis 10.3
730 rheumatoid arthritis 10.3
731 polyarteritis nodosa 10.3
732 neuroretinitis 10.3
733 multiple sclerosis 10.3
734 lyme disease 10.3
735 branch retinal artery occlusion 10.3
736 retinal artery occlusion 10.3
737 autosomal dominant cerebellar ataxia 10.3
738 hypothyroidism 10.3
739 ptosis 10.3
740 headache 10.2
741 leukemia, acute lymphoblastic 10.2
742 exanthem 10.2
743 osteomyelitis 10.2
744 b-cell lymphoma 10.2
745 scleroderma, familial progressive 10.2
746 pain sensitivity quantitative trait locus 1 10.2
747 scoliosis 10.2
748 demyelinating disease 10.2
749 uremia 10.2
750 spastic paraparesis 10.2
751 trigeminal neuralgia 10.2
752 cauda equina syndrome 10.2
753 retinitis 10.2
754 chickenpox 10.2
755 colorectal cancer 10.2
756 cryoglobulinemia, familial mixed 10.2
757 leukodystrophy 10.2
758 acquired immunodeficiency syndrome 10.2
759 mitochondrial metabolism disease 10.2
760 hypereosinophilic syndrome 10.2
761 migraine with or without aura 1 10.2
762 resting heart rate, variation in 10.2
763 human immunodeficiency virus type 1 10.2
764 spasticity 10.2
765 muscular dystrophy 10.2
766 postherpetic neuralgia 10.2
767 central retinal artery occlusion 10.2
768 color blindness 10.2
769 neuroblastoma 10.2
770 meningioma, radiation-induced 10.2
771 meningioma, familial 10.2
772 spinal meningioma 10.2
773 neuroma 10.2
774 myelitis 10.2
775 purpura 10.2
776 liver disease 10.2
777 secretory meningioma 10.2
778 lymphoplasmacyte-rich meningioma 10.2
779 fibromyalgia 10.2
780 plasma cell neoplasm 10.2
781 hepatitis c virus 10.2
782 arthritis 10.2
783 encephalitis 10.2
784 temporal arteritis 10.2
785 ocular motor apraxia 10.2
786 quadriplegia 10.2
787 herpes zoster 10.2
788 neuromyelitis optica 10.2
789 suppression amblyopia 10.2
790 amblyopia 10.2
791 myositis 10.2
792 celiac disease 1 10.2
793 nervous system disease 10.2
794 intracranial hypertension 10.2
795 encephalopathy, progressive, early-onset, with episodic rhabdomyolysis 10.2
796 uveitis 10.2
797 lactic acidosis 10.2
798 richards-rundle syndrome 10.2
799 peroxisome biogenesis disorder 1b 10.2
800 autosomal dominant intermediate charcot-marie-tooth 10.2
801 autosomal recessive intermediate charcot-marie-tooth disease 10.2
802 autosomal dominant charcot-marie-tooth disease type 2 due to kif5a mutation 10.2
803 autosomal dominant intermediate charcot-marie-tooth disease with neuropathic pain 10.2
804 autosomal dominant charcot-marie-tooth disease type 2 due to tfg mutation 10.2
805 dnajb2-related charcot-marie-tooth disease type 2 10.2
806 compartment syndrome 10.2
807 myotonic dystrophy 10.2
808 granulomatosis with polyangiitis 10.1
809 restless legs syndrome 10.1
810 graves' disease 10.1
811 systemic scleroderma 10.1
812 liver cirrhosis 10.1
813 glucose intolerance 10.1
814 neurogenic bladder 10.1
815 al amyloidosis 10.1
816 sjogren syndrome 10.1
817 pain agnosia 10.1
818 neurilemmoma 10.1
819 mitochondrial myopathy 10.1
820 chronic kidney disease 10.1
821 herpes simplex 10.1
822 crohn's disease 10.1
823 48,xyyy 10.1
824 deficiency anemia 10.1
825 small cell carcinoma 10.1
826 cranial nerve palsy 10.1
827 neurofibromatosis 10.1
828 ocular hypertension 10.1
829 hereditary transthyretin amyloidosis 10.1
830 transverse myelitis 10.1
831 back pain 10.1
832 cardiac conduction defect 10.1
833 anemia, x-linked, with or without neutropenia and/or platelet abnormalities 10.1
834 rickets 10.1
835 microscopic polyangiitis 10.1
836 atrial standstill 1 10.1
837 hypercholesterolemia, familial, 1 10.1
838 lymphoma, hodgkin, classic 10.1
839 myasthenia gravis 10.1
840 mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome 10.1
841 tetanus 10.1
842 neutropenia 10.1
843 bell's palsy 10.1
844 bilirubin metabolic disorder 10.1
845 ischemia 10.1
846 raynaud phenomenon 10.1
847 joint laxity, short stature, and myopia 10.1
848 myopia 10.1
849 arteriosclerosis 10.1
850 retinal vascular disease 10.1
851 mixed connective tissue disease 10.1
852 head injury 10.1
853 myoclonus 10.1
854 graft-versus-host disease 10.1
855 alacrima, achalasia, and mental retardation syndrome 10.1
856 leukemia 10.1
857 meningitis 10.1
858 retinal detachment 10.1
859 sexual disorder 10.1
860 macular retinal edema 10.1
861 cerebrovascular disease 10.1
862 hyperthyroidism 10.1
863 achalasia 10.1
864 aneurysm 10.1
865 hypertriglyceridemia, familial 10.1
866 leukemia, chronic lymphocytic 10.1
867 lymphoma, non-hodgkin, familial 10.1
868 body mass index quantitative trait locus 1 10.1
869 retinal vein occlusion 10.1
870 hypogonadism 10.1
871 friedreich ataxia 10.1
872 thymoma, familial 10.1
873 macular degeneration, age-related, 1 10.1
874 optic disk drusen 10.1
875 gonadal dysgenesis 10.1
876 hyperinsulinism 10.1
877 glomerulonephritis 10.1
878 thymoma 10.1
879 polymyositis 10.1
880 multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly 10.0
881 orthostatic intolerance 10.0
882 nasopharyngeal carcinoma 10.0
883 muscle hypertrophy 10.0
884 neurosarcoidosis 10.0
885 multiple cranial nerve palsy 10.0
886 acute retrobulbar neuritis 10.0
887 syphilis 10.0
888 osteosclerotic myeloma 10.0
889 spinal cord injury 10.0
890 seizures, benign familial neonatal, 1 10.0
891 lepromatous leprosy 10.0
892 keratoconjunctivitis sicca 10.0
893 foster-kennedy syndrome 10.0
894 pulmonary tuberculosis 10.0
895 adenoma 10.0
896 cytokine deficiency 10.0
897 lipomatosis, multiple 10.0
898 alkuraya-kucinskas syndrome 10.0
899 diffuse large b-cell lymphoma 10.0
900 pleomorphic lipoma 10.0
901 microcephaly 10.0
902 horner's syndrome 10.0
903 critical illness polyneuropathy 10.0
904 thrombocytopenia 10.0
905 peroneal nerve paralysis 10.0
906 ulcerative colitis 10.0
907 myeloid leukemia 10.0
908 fasciitis 10.0
909 congenital amyoplasia 10.0
910 anterior cutaneous nerve entrapment syndrome 10.0
911 breast cancer 10.0
912 strabismus 10.0
913 lung cancer 10.0
914 osteogenic sarcoma 10.0
915 optic papillitis 10.0
916 wernicke encephalopathy 10.0
917 thrombophilia 10.0
918 acute kidney failure 10.0
919 complex regional pain syndrome 10.0
920 central nervous system disease 10.0
921 plasmacytoma 10.0
922 pituitary adenoma 10.0
923 mitochondrial encephalomyopathy 10.0
924 mechanical strabismus 10.0
925 marek disease 10.0
926 cytomegalovirus infection 10.0
927 cochlear nerve deficiency 10.0
928 ovarian cancer 10.0
929 small cell cancer of the lung 10.0
930 syringomyelia, noncommunicating isolated 10.0
931 aging 10.0
932 pulmonary disease, chronic obstructive 10.0
933 aspergillosis 10.0
934 inflammatory bowel disease 10.0
935 telangiectasis 10.0
936 dementia 10.0
937 neuroaxonal dystrophy 10.0
938 acromegaly 10.0
939 thoracic outlet syndrome 10.0
940 syringomyelia 10.0
941 silent myocardial infarction 10.0
942 thyroiditis 10.0
943 arteries, anomalies of 10.0
944 homocysteinemia 10.0
945 hereditary ataxia 10.0
946 primary biliary cirrhosis 10.0
947 hepatitis b 10.0
948 keratopathy 10.0
949 adenocarcinoma 10.0
950 insulinoma 10.0
951 movement disease 10.0
952 sleep disorder 10.0
953 polycythemia 10.0
954 influenza 10.0
955 refractive error 10.0
956 sickle cell disease 10.0
957 anca-associated vasculitis 10.0
958 cerebellar degeneration 10.0
959 parkinson disease, late-onset 10.0
960 pernicious anemia 10.0
961 scapuloperoneal spinal muscular atrophy 10.0
962 body mass index quantitative trait locus 11 10.0
963 stroke, ischemic 10.0
964 reflex sympathetic dystrophy 10.0
965 mammary-digital-nail syndrome 10.0
966 leptin deficiency or dysfunction 10.0
967 peripheral artery disease 10.0
968 limb ischemia 10.0
969 plica syndrome 10.0
970 algoneurodystrophy 10.0
971 cholera 10.0
972 central retinal vein occlusion 10.0
973 synovitis 10.0
974 turner syndrome 10.0
975 aortic aneurysm 10.0
976 ileus 10.0
977 keratoconjunctivitis 10.0
978 neurofibroma 10.0
979 alopecia 10.0
980 otof-related deafness 10.0
981 depression 10.0
982 apnea, obstructive sleep 9.9
983 cardiac arrhythmia 9.9
984 multiple system atrophy 1 9.9
985 keratitis, hereditary 9.9
986 pancreatic cancer 9.9
987 diabetes mellitus, ketosis-prone 9.9
988 leukemia, acute lymphoblastic 3 9.9
989 colitis 9.9
990 fibrous dysplasia 9.9
991 osteonecrosis 9.9
992 ulnar nerve lesion 9.9
993 ehlers-danlos syndrome 9.9
994 frozen shoulder 9.9
995 hepatitis 9.9
996 hemangioma 9.9
997 tropical spastic paraparesis 9.9
998 gastritis 9.9
999 burning mouth syndrome 9.9
1000 congestive heart failure 9.9
1001 retinal degeneration 9.9
1002 collagen disease 9.9
1003 berardinelli-seip congenital lipodystrophy 9.9
1004 trpv4-associated disorders 9.9
1005 adrenomyeloneuropathy 9.9
1006 prurigo nodularis 9.9
1007 traumatic brain injury 9.9
1008 glial tumor 9.9
1009 rapidly involuting congenital hemangioma 9.9
1010 spondyloarthropathy 1 9.9
1011 atherosclerosis susceptibility 9.9
1012 meralgia paraesthetica, familial 9.9
1013 myelopathy, htlv-1-associated 9.9
1014 myoclonus and ataxia 9.9
1015 polycythemia vera 9.9
1016 coronary heart disease 1 9.9
1017 chorea, childhood-onset, with psychomotor retardation 9.9
1018 hyperlipoproteinemia, type iii 9.9
1019 gastrointestinal ulceration, recurrent, with dysfunctional platelets 9.9
1020 lipoprotein quantitative trait locus 9.9
1021 apraxia 9.9
1022 miyoshi muscular dystrophy 9.9
1023 asymptomatic neurosyphilis 9.9
1024 dermatomyositis 9.9
1025 inflammatory spondylopathy 9.9
1026 chagas disease 9.9
1027 acute leukemia 9.9
1028 choreatic disease 9.9
1029 squamous cell carcinoma 9.9
1030 viral hepatitis 9.9
1031 melanoma 9.9
1032 dermatitis 9.9
1033 early myoclonic encephalopathy 9.9
1034 pustulosis of palm and sole 9.9
1035 poliomyelitis 9.9
1036 spondylitis 9.9
1037 macular holes 9.9
1038 psoriasis 9.9
1039 glioma 9.9
1040 htlv-1 associated myelopathy/tropical spastic paraparesis 9.9
1041 mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes 9.9
1042 neurosyphilis 9.9
1043 myotonia 9.9
1044 methanol poisoning 9.9
1045 argyria 9.9
1046 aortic aneurysm, familial abdominal, 1 9.9
1047 alzheimer disease 9.9
1048 renal cell carcinoma, nonpapillary 9.9
1049 intracranial hypertension, idiopathic 9.9
1050 paine syndrome 9.9
1051 leukemia, acute myeloid 9.9
1052 body mass index quantitative trait locus 9 9.9
1053 body mass index quantitative trait locus 8 9.9
1054 body mass index quantitative trait locus 4 9.9
1055 body mass index quantitative trait locus 10 9.9
1056 anxiety 9.9
1057 body mass index quantitative trait locus 7 9.9
1058 body mass index quantitative trait locus 12 9.9
1059 body mass index quantitative trait locus 14 9.9
1060 glucocorticoid deficiency 4 with or without mineralocorticoid deficiency 9.9
1061 body mass index quantitative trait locus 18 9.9
1062 body mass index quantitative trait locus 19 9.9
1063 body mass index quantitative trait locus 20 9.9
1064 angina pectoris 9.9
1065 distal arthrogryposis 9.9
1066 meningoencephalitis 9.9
1067 hemiplegia 9.9
1068 sarcoma 9.9
1069 diphtheria 9.9
1070 aseptic meningitis 9.9
1071 tolosa-hunt syndrome 9.9
1072 ichthyosis 9.9
1073 cockayne syndrome 9.9
1074 bursitis 9.9
1075 glioblastoma multiforme 9.9
1076 progressive muscular atrophy 9.9
1077 spindle cell sarcoma 9.9
1078 perineurioma 9.9
1079 pancreatitis 9.9
1080 spinal stenosis 9.9
1081 hemophilia 9.9
1082 rheumatoid vasculitis 9.9
1083 bickerstaff brainstem encephalitis 9.9
1084 gastroesophageal reflux 9.9
1085 hirschsprung disease 1 9.9
1086 inclusion body myositis 9.9
1087 pheochromocytoma 9.9
1088 hemochromatosis, type 1 9.9
1089 insulin-like growth factor i 9.9
1090 graves disease 1 9.9
1091 xanthomatosis 9.9
1092 muscular dystrophy, congenital, lmna-related 9.9
1093 melanoma, cutaneous malignant 10 9.9
1094 lambert-eaton myasthenic syndrome 9.9
1095 lymphoplasmacytic lymphoma 9.9
1096 adrenal gland pheochromocytoma 9.9
1097 lymphoproliferative syndrome 9.9
1098 thrombosis 9.9
1099 myoglobinuria 9.9
1100 xerophthalmia 9.9
1101 hydrocephalus 9.9
1102 diabetic angiopathy 9.9
1103 nephrotic syndrome 9.9
1104 acute cystitis 9.9
1105 gout 9.9
1106 epicondylitis 9.9
1107 cerebral palsy 9.9
1108 transient cerebral ischemia 9.9
1109 lipomatosis 9.9
1110 seminoma 9.9
1111 diffuse infiltrative lymphocytosis syndrome 9.9
1112 osteoarthritis 9.9
1113 waardenburg's syndrome 9.9
1114 pulmonary embolism 9.9
1115 plantar fasciitis 9.9
1116 chromosomal triplication 9.9
1117 chronic graft versus host disease 9.9
1118 pyridoxine deficiency 9.9
1119 hypoxia 9.9
1120 chronic acquired demyelinating polyneuropathy 9.9
1121 overgrowth syndrome 9.9
1122 creutzfeldt-jakob disease 9.8
1123 thrombophilia due to thrombin defect 9.8
1124 varicose veins 9.8
1125 takayasu arteritis 9.8
1126 arachnoid cysts, intracranial 9.8
1127 psoriatic arthritis 9.8
1128 myocardial infarction 9.8
1129 riboflavin deficiency 9.8
1130 tendinitis 9.8
1131 metabolic acidosis 9.8
1132 cryptococcal meningitis 9.8
1133 covid-19 9.8
1134 castleman disease 9.8
1135 malignant hypertension 9.8
1136 pertussis 9.8
1137 heart disease 9.8
1138 clubfoot 9.8
1139 hypertrophic cardiomyopathy 9.8
1140 pancytopenia 9.8
1141 retinal ischemia 9.8
1142 hepatitis a 9.8
1143 dilated cardiomyopathy 9.8
1144 megaesophagus 9.8
1145 monoclonal paraproteinemia 9.8
1146 acrodermatitis 9.8
1147 cellulitis 9.8
1148 optic nerve sheath meningioma 9.8
1149 peptic ulcer disease 9.8
1150 carotid artery dissection 9.8
1151 iridocyclitis 9.8
1152 diabetes insipidus 9.8
1153 tenosynovitis 9.8
1154 irritable bowel syndrome 9.8
1155 toxoplasmosis 9.8
1156 mitochondrial dna-associated leigh syndrome and narp 9.8
1157 herpes zoster ophthalmicus 9.8
1158 limbic encephalitis 9.8
1159 myoclonus epilepsy 9.8
1160 splenomegaly 9.8
1161 anoxia 9.8
1162 brain injury 9.8
1163 cerebral atrophy 9.8
1164 neurotrophic keratopathy 9.8
1165 cranial neuralgia 9.8
1166 cancer-associated retinopathy 9.8
1167 neurofibromatosis, type ii 9.8
1168 pfeiffer syndrome 9.8
1169 acroosteolysis 9.8
1170 adie pupil 9.8
1171 hashimoto thyroiditis 9.8
1172 hypertelorism 9.8
1173 facioscapulohumeral muscular dystrophy 1 9.8
1174 dowling-degos disease 1 9.8
1175 torticollis 9.8
1176 biotinidase deficiency 9.8
1177 wilson disease 9.8
1178 adrenoleukodystrophy 9.8
1179 menkes disease 9.8
1180 gallbladder disease 1 9.8
1181 sickle cell anemia 9.8
1182 pars planitis 9.8
1183 anorexia nervosa 9.8
1184 hypereosinophilic syndrome, idiopathic 9.8
1185 pyruvate dehydrogenase e1-beta deficiency 9.8
1186 polymicrogyria with or without vascular-type ehlers-danlos syndrome 9.8
1187 autosomal recessive cerebellar ataxia 9.8
1188 mucositis 9.8
1189 igg4-related disease 9.8
1190 partial optic atrophy 9.8
1191 brucellosis 9.8
1192 cat-scratch disease 9.8
1193 rabies 9.8
1194 arteriovenous malformation 9.8
1195 megacolon 9.8
1196 goiter 9.8
1197 dengue disease 9.8
1198 vestibular neuronitis 9.8
1199 carotid stenosis 9.8
1200 focal segmental glomerulosclerosis 9.8
1201 hyperparathyroidism 9.8
1202 cholestasis 9.8
1203 iritis 9.8
1204 toxic shock syndrome 9.8
1205 mental depression 9.8
1206 keratosis 9.8
1207 gaucher's disease 9.8
1208 thrombocytosis 9.8
1209 spondylosis 9.8
1210 gastroenteritis 9.8
1211 severe acute respiratory syndrome 9.8
1212 human immunodeficiency virus infectious disease 9.8
1213 acute disseminated encephalomyelitis 9.8
1214 neuronitis 9.8
1215 eosinophilia-myalgia syndrome 9.8
1216 polymicrogyria 9.8
1217 scn9a neuropathic pain syndromes 9.8
1218 lymphosarcoma 9.8
1219 osteochondroma 9.8
1220 radiation induced brachial plexopathy 9.8
1221 cerebral beriberi 9.8
1222 isolated optic neuritis 9.8
1223 pik3ca-related overgrowth syndrome 9.8
1224 oculomotor apraxia 9.8
1225 thyroid carcinoma 9.8
1226 anisocoria 9.8
1227 bladder cancer 9.8
1228 burkitt lymphoma 9.8
1229 epidermoid cysts 9.8
1230 fibrosis of extraocular muscles, congenital, 1 9.8
1231 popliteal cyst 9.8
1232 prostate cancer 9.8
1233 neural tube defects 9.8
1234 spinal arachnoiditis 9.8
1235 myxedema 9.8
1236 neurodegeneration with brain iron accumulation 2a 9.8
1237 occipital horn syndrome 9.8
1238 dermatitis herpetiformis, familial 9.8
1239 propionic acidemia 9.8
1240 endometrial cancer 9.8
1241 major depressive disorder 9.8
1242 west nile virus 9.8
1243 pulmonary hypertension 9.8
1244 aspiration pneumonia 9.8
1245 brown-vialetto-van laere syndrome 9.8
1246 autism spectrum disorder 9.8
1247 cardiac arrest 9.8
1248 acrodermatitis chronica atrophicans 9.8
1249 zika fever 9.8
1250 childhood acute lymphocytic leukemia 9.8
1251 polycystic kidney disease 9.8
1252 hypogonadotropic hypogonadism 9.8
1253 postural orthostatic tachycardia syndrome 9.8
1254 venous insufficiency 9.8
1255 tuberculoid leprosy 9.8
1256 monocular esotropia 9.8
1257 chronic meningitis 9.8
1258 microphthalmia 9.8
1259 prostatic hypertrophy 9.8
1260 hypoparathyroidism 9.8
1261 disseminated intravascular coagulation 9.8
1262 choroiditis 9.8
1263 retinal vasculitis 9.8
1264 cortical blindness 9.8
1265 hemosiderosis 9.8
1266 arachnoiditis 9.8
1267 scleritis 9.8
1268 methylmalonic acidemia 9.8
1269 cystitis 9.8
1270 calcinosis 9.8
1271 status epilepticus 9.8
1272 exostosis 9.8
1273 iron metabolism disease 9.8
1274 macrocytic anemia 9.8
1275 chondroma 9.8
1276 testicular cancer 9.8
1277 causalgia 9.8
1278 mood disorder 9.8
1279 craniopharyngioma 9.8
1280 thrombophlebitis 9.8
1281 multidrug-resistant tuberculosis 9.8
1282 intraneural perineurioma 9.8
1283 intracranial hypotension 9.8
1284 brain edema 9.8
1285 cavernous hemangioma 9.8
1286 retinal disease 9.8
1287 conjunctivitis 9.8
1288 prion disease 9.8
1289 cocaine abuse 9.8
1290 night blindness 9.8
1291 lung disease 9.8
1292 dermatitis herpetiformis 9.8
1293 oropharynx cancer 9.8
1294 narcolepsy 9.8
1295 orbital disease 9.8
1296 esotropia 9.8
1297 bscl2-related neurologic disorders/seipinopathy 9.8
1298 polg-related disorders 9.8
1299 amaurosis fugax 9.8
1300 growth hormone deficiency 9.8
1301 lymphomatoid granulomatosis 9.8
1302 spastic paraplegia 17 9.8
1303 testicular seminoma 9.8
1304 seizure disorder 9.8
1305 specific language disorder 9.8
1306 autosomal recessive non-syndromic sensorineural deafness type dfnb 9.8
1307 rare tumor 9.8
1308 candidiasis, familial, 1 9.7
1309 hemifacial spasm, familial 9.7
1310 huntington disease 9.7
1311 endosteal hyperostosis, autosomal dominant 9.7
1312 melanoma, uveal 9.7
1313 myotonic dystrophy 1 9.7
1314 optic nerve hypoplasia, bilateral 9.7
1315 polykaryocytosis inducer 9.7
1316 pelvic organ prolapse 9.7
1317 thrombophilia due to activated protein c resistance 9.7
1318 triiodothyronine receptor auxiliary protein 9.7
1319 vasculitis, lymphocytic, nodular 9.7
1320 wolff-parkinson-white syndrome 9.7
1321 autism 9.7
1322 cutis marmorata telangiectatica congenita 9.7
1323 cystic fibrosis 9.7
1324 wolfram syndrome 1 9.7
1325 enterocolitis 9.7
1326 gaucher disease, type i 9.7
1327 mycosis fungoides 9.7
1328 proteasome-associated autoinflammatory syndrome 1 9.7
1329 tay-sachs disease 9.7
1330 pelizaeus-merzbacher disease 9.7
1331 deafness, nonsyndromic sensorineural, mitochondrial 9.7
1332 optic atrophy 4 9.7
1333 leukemia, chronic myeloid 9.7
1334 ewing sarcoma 9.7
1335 acute promyelocytic leukemia 9.7
1336 mantle cell lymphoma 9.7
1337 focal dystonia 9.7
1338 chronic venous insufficiency 9.7
1339 colorectal adenocarcinoma 9.7
1340 crohn's colitis 9.7
1341 atrial fibrillation 9.7
1342 inguinal hernia 9.7
1343 hereditary lymphedema i 9.7
1344 bone disease 9.7
1345 bone resorption disease 9.7
1346 cytomegalovirus retinitis 9.7
1347 tabes dorsalis 9.7
1348 sialadenitis 9.7
1349 intracranial aneurysm 9.7
1350 hypertensive retinopathy 9.7
1351 infant gynecomastia 9.7
1352 visual epilepsy 9.7
1353 esophagitis 9.7
1354 panuveitis 9.7
1355 vogt-koyanagi-harada disease 9.7
1356 bronchopneumonia 9.7
1357 pyloric stenosis 9.7
1358 acoustic neuroma 9.7
1359 gynecomastia 9.7
1360 leiomyoma 9.7
1361 hypermobility syndrome 9.7
1362 acute closed-angle glaucoma 9.7
1363 neovascular glaucoma 9.7
1364 duodenal ulcer 9.7
1365 retinal vascular occlusion 9.7
1366 rectum cancer 9.7
1367 enthesopathy 9.7
1368 relapsing-remitting multiple sclerosis 9.7
1369 granulomatous angiitis 9.7
1370 relapsing polychondritis 9.7
1371 myoma 9.7
1372 capillary hemangioma 9.7
1373 glycogen storage disease 9.7
1374 acute pancreatitis 9.7
1375 membranoproliferative glomerulonephritis 9.7
1376 primary hyperoxaluria 9.7
1377 malignant glioma 9.7
1378 vaccinia 9.7
1379 carotid artery disease 9.7
1380 mammary paget's disease 9.7
1381 breast adenocarcinoma 9.7
1382 cavernous sinus thrombosis 9.7
1383 hypertrichosis 9.7
1384 hepatitis e 9.7
1385 rhinitis 9.7
1386 hypokalemia 9.7
1387 calciphylaxis 9.7
1388 benign ependymoma 9.7
1389 infertility 9.7
1390 cellular ependymoma 9.7
1391 lymphopenia 9.7
1392 osteochondrosis 9.7
1393 septic arthritis 9.7
1394 periodontitis 9.7
1395 mucormycosis 9.7
1396 bullous pemphigoid 9.7
1397 chronic fatigue syndrome 9.7
1398 eating disorder 9.7
1399 decubitus ulcer 9.7
1400 homocystinuria 9.7
1401 glaucomatocyclitic crisis 9.7
1402 acute myocardial infarction 9.7
1403 fatty liver disease 9.7
1404 vitreous detachment 9.7
1405 hypersensitivity vasculitis 9.7
1406 nonsyndromic deafness 9.7
1407 dfnx1 nonsyndromic hearing loss and deafness 9.7
1408 dnmt1-related disorder 9.7
1409 hypermobile ehlers-danlos syndrome 9.7
1410 isolated methylmalonic acidemia 9.7
1411 gigantism 9.7
1412 heavy metal poisoning 9.7
1413 multifocal choroiditis 9.7
1414 ovarian epithelial cancer 9.7
1415 primary orthostatic hypotension 9.7
1416 pudendal neuralgia 9.7
1417 undifferentiated connective tissue disease 9.7
1418 age-related hearing loss 9.7
1419 cerebral aneurysms 9.7
1420 hemifacial spasm 9.7
1421 systemic autoimmune disease 9.7
1422 paraneoplastic sensory ganglionopathy 9.7
1423 spontaneous intracranial hypotension 9.7
1424 abducens palsy 9.7
1425 hypertension, essential 9.7
1426 lentigines 9.7
1427 macrodactyly 9.7
1428 metatropic dysplasia 9.7
1429 neurofibromatosis, type i 9.7
1430 otitis media 9.7
1431 peroneal nerve, accessory deep 9.7
1432 mccune-albright syndrome 9.7
1433 pseudopapilledema 9.7
1434 spastic paraplegia 4, autosomal dominant 9.7
1435 spondylosis, cervical 9.7
1436 vitiligo-associated multiple autoimmune disease susceptibility 6 9.7
1437 zinc finger protein 1 9.7
1438 chordoma 9.7
1439 congenital heart defects, hamartomas of tongue, and polysyndactyly 9.7
1440 3-hydroxyacyl-coa dehydrogenase deficiency 9.7
1441 gitelman syndrome 9.7
1442 pseudoxanthoma elasticum 9.7
1443 reticulum cell sarcoma 9.7
1444 tardive dyskinesia 9.7
1445 squamous cell carcinoma, head and neck 9.7
1446 werner syndrome 9.7
1447 wernicke-korsakoff syndrome 9.7
1448 fragile x tremor/ataxia syndrome 9.7
1449 corpus callosum, partial agenesis of, x-linked 9.7
1450 optic atrophy 2 9.7
1451 retinoschisis 1, x-linked, juvenile 9.7
1452 warburg micro syndrome 1 9.7
1453 helicobacter pylori infection 9.7
1454 intervertebral disc disease 9.7
1455 renal cell carcinoma, papillary, 1 9.7
1456 hypertension, early-onset, autosomal dominant, with severe exacerbation in pregnancy 9.7
1457 vitiligo-associated multiple autoimmune disease susceptibility 1 9.7
1458 angioid streaks 9.7
1459 muscular dystrophy, congenital merosin-deficient, 1a 9.7
1460 legionnaire disease 9.7
1461 lipodystrophy, congenital generalized, type 1 9.7
1462 primary lateral sclerosis, adult, 1 9.7
1463 lung cancer susceptibility 3 9.7
1464 fatty liver disease, nonalcoholic 1 9.7
1465 gastric cancer 9.7
1466 dengue virus 9.7
1467 membranous nephropathy 9.7
1468 livedoid vasculitis 9.7
1469 invasive aspergillosis 9.7
1470 hypophosphatemia 9.7
1471 epidemic typhus 9.7
1472 short qt syndrome 9.7
1473 cervical dystonia 9.7
1474 fibroma 9.7
1475 cogan syndrome 9.7
1476 crest syndrome 9.7
1477 pontocerebellar hypoplasia 9.7
1478 adenoid cystic carcinoma 9.7
1479 aortic dissection 9.7
1480 dopamine beta-hydroxylase deficiency 9.7
1481 keratoconus 9.7
1482 thalassemia 9.7
1483 bacterial infectious disease 9.7
1484 osteomalacia 9.7
1485 pre-eclampsia 9.7
1486 primary optic atrophy 9.7
1487 portal hypertension 9.7
1488 gastric ulcer 9.7
1489 enophthalmos 9.7
1490 pituitary apoplexy 9.7
1491 retinal microaneurysm 9.7
1492 adult respiratory distress syndrome 9.7
1493 pyelonephritis 9.7
1494 alternating exotropia 9.7
1495 exotropia 9.7
1496 hemopericardium 9.7
1497 gestational diabetes 9.7
1498 prediabetes syndrome 9.7
1499 emery-dreifuss muscular dystrophy 9.7
1500 pericardial effusion 9.7
1501 low compliance bladder 9.7
1502 common variable immunodeficiency 9.7
1503 secondary hyperparathyroidism 9.7
1504 hepatic coma 9.7
1505 hypertrophic pyloric stenosis 9.7
1506 background diabetic retinopathy 9.7
1507 megaloblastic anemia 9.7
1508 paranasal sinus disease 9.7
1509 amenorrhea 9.7
1510 primary angle-closure glaucoma 9.7
1511 noonan syndrome with multiple lentigines 9.7
1512 generalized anxiety disorder 9.7
1513 neuroleptic malignant syndrome 9.7
1514 candidiasis 9.7
1515 urticaria 9.7
1516 communicating hydrocephalus 9.7
1517 lymphadenitis 9.7
1518 pneumothorax 9.7
1519 neuroendocrine tumor 9.7
1520 epilepsy 9.7
1521 autoimmune hepatitis 9.7
1522 hyperostosis 9.7
1523 essential thrombocythemia 9.7
1524 colon adenocarcinoma 9.7
1525 kernicterus 9.7
1526 protein s deficiency 9.7
1527 transitional cell carcinoma 9.7
1528 pigmented villonodular synovitis 9.7
1529 tic disorder 9.7
1530 contact dermatitis 9.7
1531 prostatic adenoma 9.7
1532 endometriosis 9.7
1533 substance abuse 9.7
1534 multiple endocrine neoplasia 9.7
1535 cutis laxa 9.7
1536 lysosomal storage disease 9.7
1537 thymic carcinoma 9.7
1538 temporal lobe epilepsy 9.7
1539 bone inflammation disease 9.7
1540 fibrosarcoma 9.7
1541 histiocytosis 9.7
1542 skin carcinoma 9.7
1543 skin disease 9.7
1544 extraskeletal chondroma 9.7
1545 restrictive cardiomyopathy 9.7
1546 essential tremor 9.7
1547 nephrolithiasis 9.7
1548 eosinophilic pneumonia 9.7
1549 severe combined immunodeficiency 9.7
1550 inherited metabolic disorder 9.7
1551 t-cell lymphoblastic leukemia/lymphoma 9.7
1552 carotid artery occlusion 9.7
1553 myocarditis 9.7
1554 paralytic ileus 9.7
1555 pellagra 9.7
1556 hodgkin's lymphoma, lymphocytic-histiocytic predominance 9.7
1557 malignant hyperthermia 9.7
1558 rubella 9.7
1559 skin melanoma 9.7
1560 atrophic gastritis 9.7
1561 gas gangrene 9.7
1562 herpes zoster oticus 9.7
1563 primary cerebellar degeneration 9.7
1564 status asthmaticus 9.7
1565 hypopituitarism 9.7
1566 bronchiectasis 9.7
1567 necrotizing fasciitis 9.7
1568 villonodular synovitis 9.7
1569 albinism 9.7
1570 limb-girdle muscular dystrophy 9.7
1571 lama2-related muscular dystrophy 9.7
1572 spastic paraplegia 4 9.7
1573 trichorhinophalangeal syndrome 9.7
1574 allergic encephalomyelitis 9.7
1575 athetosis 9.7
1576 broken heart syndrome 9.7
1577 central serous chorioretinopathy 9.7
1578 cerebrospinal fluid leak 9.7
1579 chiari malformation 9.7
1580 chromophil renal cell carcinoma 9.7
1581 cluster headache 9.7
1582 cutaneous polyarteritis nodosa 9.7
1583 dentinogenesis imperfecta type 2 9.7
1584 glossodynia 9.7
1585 harlequin syndrome 9.7
1586 human t-cell leukemia virus type 1 9.7
1587 hypoganglionosis 9.7
1588 leukemia, t-cell, chronic 9.7
1589 light chain deposition disease 9.7
1590 melanoma-associated retinopathy 9.7
1591 mercury poisoning 9.7
1592 rosai-dorfman disease 9.7
1593 skeletal dysplasias 9.7
1594 st anthony's fire 9.7
1595 tarlov cysts 9.7
1596 bunion 9.7
1597 color vision deficiency 9.7
1598 nonsyndromic hearing loss 9.7
1599 pituitary tumors 9.7
1600 paraneoplastic limbic encephalitis 9.7
1601 b-cell non-hodgkin lymphoma 9.7
1602 rare neurodegenerative disease 9.7
1603 acute transverse myelitis 9.7
1604 cerebrofacial arteriovenous metameric syndrome 9.7
1605 temporomandibular joint anomaly 9.7
1606 cyanide poisoning 9.7
1607 secondary vasculitis 9.7
1608 neuroendocrine neoplasm of pancreas 9.7
1609 familial short qt syndrome 9.7
1610 acute liver failure 9.7
1611 acanthosis nigricans 9.6
1612 blood group--newfoundland 9.6
1613 progressive familial heart block, type ia 9.6
1614 hepatocellular carcinoma 9.6
1615 cardiofaciocutaneous syndrome 1 9.6
1616 cervical rib 9.6
1617 chlorpropamide-alcohol flushing 9.6
1618 cleft palate, isolated 9.6
1619 deafness, unilateral 9.6
1620 cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1 9.6
1621 dentatorubral-pallidoluysian atrophy 9.6
1622 discrimination, two-point, reduction in 9.6
1623 camurati-engelmann disease 9.6
1624 exudative vitreoretinopathy 1 9.6
1625 gilles de la tourette syndrome 9.6
1626 hand skill, relative 9.6
1627 spondyloepiphyseal dysplasia with congenital joint dislocations 9.6
1628 kaposi sarcoma 9.6
1629 leiomyoma, uterine 9.6
1630 macroglossia 9.6
1631 thyroid carcinoma, familial medullary 9.6
1632 medulloblastoma 9.6
1633 renal failure, progressive, with hypertension 9.6
1634 noonan syndrome 1 9.6
1635 hemifacial microsomia 9.6
1636 spinocerebellar ataxia 7 9.6
1637 osteoporosis 9.6
1638 nephrolithiasis, calcium oxalate 9.6
1639 perry syndrome 9.6
1640 posterior column ataxia 9.6
1641 hutchinson-gilford progeria syndrome 9.6
1642 raynaud disease 9.6
1643 retinoblastoma 9.6
1644 schizophrenia 9.6
1645 spondylolisthesis 9.6
1646 spondyloepimetaphyseal dysplasia, strudwick type 9.6
1647 spondylometaphyseal dysplasia, kozlowski type 9.6
1648 stiff-person syndrome 9.6
1649 sturge-weber syndrome 9.6
1650 chromosome 2q35 duplication syndrome 9.6
1651 tobacco addiction 9.6
1652 acrodermatitis enteropathica, zinc-deficiency type 9.6
1653 australia antigen 9.6
1654 gordon holmes syndrome 9.6
1655 cockayne syndrome a 9.6
1656 eosinophilic fasciitis 9.6
1657 galactosemia i 9.6
1658 glycogen storage disease ii 9.6
1659 homocystinuria due to deficiency of n -methylenetetrahydrofolate reductase activity 9.6
1660 acetylation, slow 9.6
1661 myelofibrosis 9.6
1662 myopathy, congenital 9.6
1663 pulmonic stenosis 9.6
1664 dihydropyrimidine dehydrogenase deficiency 9.6
1665 spastic paraplegia 20, autosomal recessive 9.6
1666 xeroderma pigmentosum, variant type 9.6
1667 de sanctis-cacchione syndrome 9.6
1668 phosphoribosylpyrophosphate synthetase superactivity 9.6
1669 deafness, x-linked 1 9.6
1670 muscular dystrophy, duchenne type 9.6
1671 tooth size 9.6
1672 retinitis pigmentosa-deafness syndrome 9.6
1673 cyclic vomiting syndrome 9.6
1674 deafness, aminoglycoside-induced 9.6
1675 wolfram syndrome, mitochondrial form 9.6
1676 prostatic hyperplasia, benign 9.6
1677 supranuclear palsy, progressive, 1 9.6
1678 suppression of tumorigenicity 12 9.6
1679 wilms tumor 5 9.6
1680 ventricular fibrillation, paroxysmal familial, 1 9.6
1681 systemic lupus erythematosus 2 9.6
1682 abdominal obesity-metabolic syndrome 1 9.6
1683 maturity-onset diabetes of the young 9.6
1684 spongiform encephalopathy with neuropsychiatric features 9.6
1685 gastrointestinal stromal tumor 9.6
1686 leprosy 2 9.6
1687 mycobacterium tuberculosis 1 9.6
1688 kala-azar 1 9.6
1689 spinocerebellar ataxia 28 9.6
1690 malaria 9.6
1691 bone mineral density quantitative trait locus 8 9.6
1692 smoking as a quantitative trait locus 3 9.6
1693 major affective disorder 8 9.6
1694 major affective disorder 9 9.6
1695 hearing loss, noise-induced 9.6
1696 bone mineral density quantitative trait locus 15 9.6
1697 myelodysplastic syndrome 9.6
1698 cardiofaciocutaneous syndrome 2 9.6
1699 episodic pain syndrome, familial, 3 9.6
1700 spastic paraplegia, intellectual disability, nystagmus, and obesity 9.6
1701 mucopolysaccharidosis-plus syndrome 9.6
1702 tendinopathy 9.6
1703 peyronie's disease 9.6
1704 chlamydia pneumonia 9.6
1705 chikungunya 9.6
1706 cutaneous lupus erythematosus 9.6
1707 tick-borne encephalitis 9.6
1708 foodborne botulism 9.6
1709 usher syndrome 9.6
1710 brugada syndrome 9.6
1711 adult t-cell leukemia 9.6
1712 female breast cancer 9.6
1713 brachyolmia 9.6
1714 cone dystrophy 9.6
1715 atrioventricular block 9.6
1716 focal hand dystonia 9.6
1717 diabetic encephalopathy 9.6
1718 tonsil squamous cell carcinoma 9.6
1719 immunoglobulin alpha deficiency 9.6
1720 heavy chain disease 9.6
1721 gamma heavy chain disease 9.6
1722 diffuse alopecia areata 9.6
1723 ileitis 9.6
1724 warburg micro syndrome 9.6
1725 gallbladder disease 9.6
1726 hypomyelinating leukodystrophy 9.6
1727 dry beriberi 9.6
1728 ocular tuberculosis 9.6
1729 x-linked recessive disease 9.6
1730 chronic myelomonocytic leukemia 9.6
1731 neurodegeneration with brain iron accumulation 9.6
1732 type 1 diabetes mellitus 3 9.6
1733 type 1 diabetes mellitus 10 9.6
1734 migraine with aura 9.6
1735 trypanosomiasis 9.6
1736 cholelithiasis 9.6
1737 endocarditis 9.6
1738 silicosis 9.6
1739 siderosis 9.6
1740 common cold 9.6
1741 gastric lymphoma 9.6
1742 interstitial nephritis 9.6
1743 renal hypertension 9.6
1744 primary polycythemia 9.6
1745 methemoglobinemia 9.6
1746 amnestic disorder 9.6
1747 corneal edema 9.6
1748 primary hyperparathyroidism 9.6
1749 orbital cellulitis 9.6
1750 chlamydia 9.6
1751 pneumocystosis 9.6
1752 pulmonary edema 9.6
1753 iron deficiency anemia 9.6
1754 synostosis 9.6
1755 conn's syndrome 9.6
1756 detrusor sphincter dyssynergia 9.6
1757 dengue hemorrhagic fever 9.6
1758 paranoid schizophrenia 9.6
1759 dysentery 9.6
1760 tibial nerve palsy 9.6
1761 hemolytic-uremic syndrome 9.6
1762 posterior uveitis 9.6
1763 olecranon bursitis 9.6
1764 hereditary spherocytosis 9.6
1765 renal osteodystrophy 9.6
1766 periventricular leukomalacia 9.6
1767 exocrine pancreatic insufficiency 9.6
1768 hyperinsulinemic hypoglycemia 9.6
1769 diabetic cataract 9.6
1770 pulmonary sarcoidosis 9.6
1771 hepatic encephalopathy 9.6
1772 kwashiorkor 9.6
1773 mature cataract 9.6
1774 facial neuralgia 9.6
1775 de quervain disease 9.6
1776 renal tubular acidosis 9.6
1777 azoospermia 9.6
1778 adult-onset still's disease 9.6
1779 shoulder impingement syndrome 9.6
1780 glossopharyngeal neuralgia 9.6
1781 46 xx gonadal dysgenesis 9.6
1782 lymphangioma 9.6
1783 echinococcosis 9.6
1784 panniculitis 9.6
1785 thrombocytopenia due to platelet alloimmunization 9.6
1786 mitral valve stenosis 9.6
1787 pericarditis 9.6
1788 ossifying fibroma 9.6
1789 urethral stricture 9.6
1790 hyperuricemia 9.6
1791 sphingolipidosis 9.6
1792 leiomyosarcoma 9.6
1793 hereditary multiple exostoses 9.6
1794 ectodermal dysplasia 9.6
1795 dental caries 9.6
1796 ankylosis 9.6
1797 pharyngitis 9.6
1798 basal cell carcinoma 9.6
1799 hematologic cancer 9.6
1800 chronic inflammatory demyelinating polyneuritis 9.6
1801 corneal dystrophy 9.6
1802 epidermolysis bullosa 9.6
1803 glucosephosphate dehydrogenase deficiency 9.6
1804 laryngeal squamous cell carcinoma 9.6
1805 anuria 9.6
1806 astrocytoma 9.6
1807 interstitial lung disease 9.6
1808 papillary carcinoma 9.6
1809 spinal cord disease 9.6
1810 neurilemmomatosis 9.6
1811 gastric dilatation 9.6
1812 central nervous system lymphoma 9.6
1813 rhabdomyosarcoma 9.6
1814 germinoma 9.6
1815 embryonal carcinoma 9.6
1816 bipolar disorder 9.6
1817 gm2 gangliosidosis 9.6
1818 liposarcoma 9.6
1819 palmoplantar keratosis 9.6
1820 cerebritis 9.6
1821 empty sella syndrome 9.6
1822 olfactory neuroblastoma 9.6
1823 gastric adenocarcinoma 9.6
1824 thyroid gland medullary carcinoma 9.6
1825 pancreatic adenocarcinoma 9.6
1826 heart valve disease 9.6
1827 persian gulf syndrome 9.6
1828 familial retinoblastoma 9.6
1829 rapidly progressive glomerulonephritis 9.6
1830 elephantiasis 9.6
1831 optic nerve glioma 9.6
1832 myxopapillary ependymoma 9.6
1833 copper deficiency myelopathy 9.6
1834 nutritional deficiency disease 9.6
1835 pneumonia 9.6
1836 chiasmal syndrome 9.6
1837 hemolytic anemia 9.6
1838 malignant peripheral nerve sheath tumor 9.6
1839 bronchitis 9.6
1840 progressive multifocal leukoencephalopathy 9.6
1841 juvenile pilocytic astrocytoma 9.6
1842 tuberculum sellae meningioma 9.6
1843 peritonitis 9.6
1844 pyridoxine deficiency anemia 9.6
1845 localized scleroderma 9.6
1846 measles 9.6
1847 subacute delirium 9.6
1848 intermediate coronary syndrome 9.6
1849 chorioretinitis 9.6
1850 progressive myoclonus epilepsy 9.6
1851 learning disability 9.6
1852 degenerative disc disease 9.6
1853 leishmaniasis 9.6
1854 central sleep apnea 9.6
1855 cleft lip 9.6
1856 orbital plasma cell granuloma 9.6
1857 exposure keratitis 9.6
1858 stomatitis 9.6
1859 interstitial keratitis 9.6
1860 atp7a-related copper transport disorders 9.6
1861 childhood ataxia with central nervous system hypomyelination / vanishing white matter 9.6
1862 hereditary multiple osteochondromas 9.6
1863 mpv17-related mitochondrial dna maintenance defect 9.6
1864 ngly1-related congenital disorder of deglycosylation 9.6
1865 plp1 disorders 9.6
1866 rab18 deficiency 9.6
1867 wfs1 wolfram syndrome spectrum disorder 9.6
1868 acute graft versus host disease 9.6
1869 acute monoblastic leukemia 9.6
1870 acute zonal occult outer retinopathy 9.6
1871 amyloidosis aa 9.6
1872 autoimmune encephalitis 9.6
1873 charcot-marie-tooth disease type 2l 9.6
1874 charles bonnet syndrome 9.6
1875 chromosome 17p duplication 9.6
1876 chronic polyradiculoneuritis 9.6
1877 cold agglutinin disease 9.6
1878 cramp-fasciculation syndrome 9.6
1879 dfnb1 9.6
1880 diffuse cutaneous systemic sclerosis 9.6
1881 enteropathica 9.6
1882 gangliosidosis 9.6
1883 homologous wasting disease 9.6
1884 hyperacusis 9.6
1885 hypoaldosteronism 9.6
1886 lathyrism 9.6
1887 lymphocytic hypophysitis 9.6
1888 macrophage activation syndrome 9.6
1889 meningococcemia 9.6
1890 persistent genital arousal disorder 9.6
1891 pontine hemorrhage 9.6
1892 precocious puberty 9.6
1893 primary central nervous system lymphoma 9.6
1894 pseudo-turner syndrome 9.6
1895 retroperitoneal fibrosis 9.6
1896 sacral plexopathy 9.6
1897 sinonasal undifferentiated carcinoma 9.6
1898 sticky platelet syndrome 9.6
1899 synovial chondromatosis 9.6
1900 tuberculous meningitis 9.6
1901 weber syndrome 9.6
1902 early-onset glaucoma 9.6
1903 angiomatosis 9.6
1904 cavernous malformation 9.6
1905 cumulative trauma disorders 9.6
1906 hypertonia 9.6
1907 myopathy - thyrotoxic 9.6
1908 overuse syndrome 9.6
1909 repetitive motion disorders 9.6
1910 spinal cord infarction 9.6
1911 werdnig-hoffman disease 9.6
1912 whiplash 9.6
1913 subacute cutaneous lupus erythematosus 9.6
1914 inflammatory myopathy with abundant macrophages 9.6
1915 46,xy partial gonadal dysgenesis 9.6
1916 drug-induced vasculitis 9.6
1917 muscular lipidosis 9.6
1918 periodic paralysis 9.6
1919 progressive muscular dystrophy 9.6
1920 idiopathic uveal effusion syndrome 9.6
1921 rare hereditary hemochromatosis 9.6
1922 toxic oil syndrome 9.6
1923 autosomal recessive spastic ataxia 9.6
1924 acyl-coa dehydrogenase deficiency 9.6
1925 igg4-related ophthalmic disease 9.6
1926 igg4-related pachymeningitis 9.6
1927 avascular necrosis 9.6
1928 persistent idiopathic facial pain 9.6
1929 serotonin syndrome 9.6
1930 discoid lupus erythematosus 9.6
1931 transient pseudohypoaldosteronism 9.6
1932 premature aging 9.6
1933 erythrokeratoderma 9.6
1934 type ii mixed cryoglobulinemia 9.6
1935 pediatric systemic lupus erythematosus 9.6
1936 complex hereditary spastic paraplegia 9.6
1937 pure hereditary spastic paraplegia 9.6
1938 hajdu-cheney syndrome 9.4
1939 cerebral amyloid angiopathy, cst3-related 9.4
1940 amyloidosis, familial visceral 9.4
1941 angioedema, hereditary, type i 9.4
1942 aplasia cutis congenita, nonsyndromic 9.4
1943 atrial tachyarrhythmia with short pr interval 9.4
1944 behcet syndrome 9.4
1945 blue rubber bleb nevus 9.4
1946 hypercarotenemia and vitamin a deficiency, autosomal dominant 9.4
1947 sotos syndrome 1 9.4
1948 charcot-marie-tooth disease, guadalajara neuronal type 9.4
1949 cherubism 9.4
1950 chiari malformation type i 9.4
1951 alagille syndrome 1 9.4
1952 clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly 9.4
1953 coloboma of macula 9.4
1954 complement component 4, partial deficiency of 9.4
1955 cone-rod dystrophy 2 9.4
1956 cri-du-chat syndrome 9.4
1957 deafness, autosomal dominant 1 9.4
1958 dupuytren contracture 9.4
1959 ear flare 9.4
1960 ear malformation 9.4
1961 ehlers-danlos syndrome, hypermobility type 9.4
1962 multiple self-healing squamous epithelioma 9.4
1963 erythrocytosis, familial, 1 9.4
1964 erythrokeratodermia variabilis et progressiva 1 9.4
1965 esophageal cancer 9.4
1966 facial spasm 9.4
1967 fanconi renotubular syndrome 1 9.4
1968 fibrodysplasia ossificans progressiva 9.4
1969 hair whorl 9.4
1970 hemifacial atrophy, progressive 9.4
1971 hyperalphalipoproteinemia 1 9.4
1972 ichthyosis vulgaris 9.4
1973 ige responsiveness, atopic 9.4
1974 intussusception 9.4
1975 keratitis-ichthyosis-deafness syndrome, autosomal dominant 9.4
1976 klippel-trenaunay-weber syndrome 9.4
1977 laryngeal abductor paralysis 9.4
1978 laryngomalacia 9.4
1979 legg-calve-perthes disease 9.4
1980 masticatory muscles, hypertrophy of 9.4
1981 melkersson-rosenthal syndrome 9.4
1982 meniere disease 9.4
1983 metaphyseal chondrodysplasia, schmid type 9.4
1984 nondisjunction 9.4
1985 spinal muscular atrophy, lower extremity-predominant, 1, autosomal dominant 9.4
1986 multiple endocrine neoplasia, type iib 9.4
1987 neutrophilia, hereditary 9.4
1988 ocular dominance 9.4
1989 obsessive-compulsive disorder 9.4
1990 multicentric carpotarsal osteolysis syndrome 9.4
1991 parastremmatic dwarfism 9.4
1992 polyposis, skin pigmentation, alopecia, and fingernail changes 9.4
1993 proteus syndrome 9.4
1994 protoporphyria, erythropoietic, 1 9.4
1995 pulmonary hypertension, primary, 1 9.4
1996 pyloric stenosis, infantile hypertrophic, 1 9.4
1997 emery-dreifuss muscular dystrophy 2, autosomal dominant 9.4
1998 scoliosis, isolated 1 9.4
1999 thrombocytopenic purpura, autoimmune 9.4
2000 thyroid cancer, nonmedullary, 1 9.4
2001 trichomegaly 9.4
2002 down syndrome 9.4
2003 tritanopia 9.4
2004 suppressor of tumorigenicity 3 9.4
2005 carpenter syndrome 1 9.4
2006 acyl-coa dehydrogenase, short-chain, deficiency of 9.4
2007 alexander disease 9.4
2008 alstrom syndrome 9.4
2009 anemia, autoimmune hemolytic 9.4
2010 bardet-biedl syndrome 1 9.4
2011 buerger disease 9.4
2012 fazio-londe disease 9.4
2013 carnitine deficiency, myopathic 9.4
2014 peroxisome biogenesis disorder 1a 9.4
2015 charge syndrome 9.4
2016 bile acid synthesis defect, congenital, 4 9.4
2017 chondrosarcoma 9.4
2018 boucher-neuhauser syndrome 9.4
2019 corpus callosum, agenesis of 9.4
2020 pituitary adenoma 4, acth-secreting 9.4
2021 dandy-walker syndrome 9.4
2022 deafness, autosomal recessive 1a 9.4
2023 deafness, onychodystrophy, osteodystrophy, mental retardation, and seizures syndrome 9.4
2024 diastematomyelia 9.4
2025 duodenal atresia 9.4
2026 schopf-schulz-passarge syndrome 9.4
2027 ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive 9.4
2028 epidermolysis bullosa dystrophica, autosomal recessive 9.4
2029 factor vii deficiency 9.4
2030 fructose intolerance, hereditary 9.4
2031 galactorrhea 9.4
2032 multiple acyl-coa dehydrogenase deficiency 9.4
2033 glycogen storage disease iii 9.4
2034 perrault syndrome 1 9.4
2035 hemihyperplasia, isolated 9.4
2036 hemolytic uremic syndrome, atypical 1 9.4
2037 urofacial syndrome 1 9.4
2038 hypoascorbemia 9.4
2039 kuru 9.4
2040 miller-dieker lissencephaly syndrome 9.4
2041 macrocephaly/megalencephaly syndrome, autosomal recessive 9.4
2042 maple syrup urine disease 9.4
2043 familial mediterranean fever 9.4
2044 megacystis-microcolon-intestinal hypoperistalsis syndrome 9.4
2045 thiamine-responsive megaloblastic anemia syndrome 9.4
2046 methane production 9.4
2047 microcolon 9.4
2048 moyamoya disease 1 9.4
2049 mucolipidosis iii alpha/beta 9.4
2050 myoclonic epilepsy of lafora 9.4
2051 myoclonic epilepsy of unverricht and lundborg 9.4
2052 galactosialidosis 9.4
2053 neuraminidase deficiency 9.4
2054 niemann-pick disease, type c1 9.4
2055 hyperoxaluria, primary, type i 9.4
2056 hyperoxaluria, primary, type ii 9.4
2057 pancreatic agenesis 1 9.4
2058 subacute sclerosing panencephalitis 9.4
2059 d-bifunctional protein deficiency 9.4
2060 abnormal hair, joint laxity, and developmental delay 9.4
2061 polycystic kidney disease 4 with or without polycystic liver disease 9.4
2062 sandhoff disease 9.4
2063 spinocerebellar ataxia, autosomal recessive 3 9.4
2064 asplenia, isolated congenital 9.4
2065 hypothyroidism, congenital, nongoitrous, 4 9.4
2066 restrictive dermopathy, lethal 9.4
2067 chanarin-dorfman syndrome 9.4
2068 usher syndrome, type i 9.4
2069 methylmalonic aciduria and homocystinuria, cblc type 9.4
2070 waardenburg syndrome, type 4a 9.4
2071 xeroderma pigmentosum, complementation group a 9.4
2072 muscular dystrophy, becker type 9.4
2073 albinism-deafness syndrome 9.4
2074 spinal muscular atrophy, x-linked 2 9.4
2075 tubulin, beta 9.4
2076 charcot-marie-tooth peroneal muscular atrophy, x-linked, with aplasia cutis congenita 9.4
2077 choroideremia 9.4
2078 hemophilia b 9.4
2079 incontinentia pigmenti 9.4
2080 lowe oculocerebrorenal syndrome 9.4
2081 linear skin defects with multiple congenital anomalies 1 9.4
2082 myopathy, centronuclear, x-linked 9.4
2083 properdin deficiency, x-linked 9.4
2084 rett syndrome 9.4
2085 spastic paraplegia 2, x-linked 9.4
2086 spinal and bulbar muscular atrophy, x-linked 1 9.4
2087 diabetes and deafness, maternally inherited 9.4
2088 oncocytoma 9.4
2089 parkinson disease, mitochondrial 9.4
2090 epilepsy, childhood absence 1 9.4
2091 epiphyseal dysplasia, multiple, 2 9.4
2092 frontotemporal dementia 9.4
2093 aminopterin syndrome sine aminopterin 9.4
2094 deafness, autosomal dominant 4a 9.4
2095 d-2-hydroxyglutaric aciduria 1 9.4
2096 budd-chiari syndrome 9.4
2097 glaucoma 3, primary infantile, b 9.4
2098 deafness, autosomal dominant 5 9.4
2099 agammaglobulinemia 1, autosomal recessive 9.4
2100 stuve-wiedemann syndrome 9.4
2101 amyotrophy, monomelic 9.4
2102 rigid spine muscular dystrophy 1 9.4
2103 dermatitis, atopic 9.4
2104 leukoencephalopathy with vanishing white matter 9.4
2105 megalencephalic leukoencephalopathy with subcortical cysts 1 9.4
2106 keratosis pilaris atrophicans 9.4
2107 spastic paraplegia 11, autosomal recessive 9.4
2108 cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 9.4
2109 progressive familial heart block, type ib 9.4
2110 panbronchiolitis, diffuse 9.4
2111 langerhans cell histiocytosis 9.4
2112 spastic paraplegia 14, autosomal recessive 9.4
2113 nonaka myopathy 9.4
2114 aneurysmal bone cysts 9.4
2115 spinocerebellar ataxia 15 9.4
2116 kufor-rakeb syndrome 9.4
2117 allergic rhinitis 9.4
2118 microcephaly, amish type 9.4
2119 epileptic encephalopathy, early infantile, 6 9.4
2120 spinocerebellar ataxia 21 9.4
2121 bulimia nervosa 9.4
2122 ovarian cancer 1 9.4
2123 diabetes mellitus, noninsulin-dependent, 4 9.4
2124 neutrophilic dermatosis, acute febrile 9.4
2125 tropical calcific pancreatitis 9.4
2126 myopathy, myosin storage, autosomal dominant 9.4
2127 hypertension, diastolic 9.4
2128 spinocerebellar ataxia 20 9.4
2129 spondyloepimetaphyseal dysplasia, matrilin-3 related 9.4
2130 spinocerebellar ataxia 8 9.4
2131 avascular necrosis of femoral head, primary, 1 9.4
2132 myopia 6 9.4
2133 choanal atresia, posterior 9.4
2134 aplastic anemia 9.4
2135 erythroderma, ichthyosiform, congenital reticular 9.4
2136 syndactyly, mesoaxial synostotic, with phalangeal reduction 9.4
2137 goldberg-shprintzen syndrome 9.4
2138 testicular microlithiasis 9.4
2139 combined oxidative phosphorylation deficiency 3 9.4
2140 potocki-lupski syndrome 9.4
2141 xfe progeroid syndrome 9.4
2142 congenital disorder of glycosylation, type in 9.4
2143 hemolytic anemia, cd59-mediated, with or without immune-mediated polyneuropathy 9.4
2144 epilepsy, progressive myoclonic, 1b 9.4
2145 multiple sclerosis 2 9.4
2146 neurodegeneration due to cerebral folate transport deficiency 9.4
2147 spastic paraplegia 36, autosomal dominant 9.4
2148 fanconi renotubular syndrome 2 9.4
2149 alpha-1-antitrypsin deficiency 9.4
2150 ectodermal dysplasia-syndactyly syndrome 2 9.4
2151 tuberculin skin test reactivity, absence of 9.4
2152 thiamine metabolism dysfunction syndrome 4 9.4
2153 cyanosis, transient neonatal 9.4
2154 myopia, high, with cataract and vitreoretinal degeneration 9.4
2155 pseudohypoaldosteronism, type iie 9.4
2156 thrombocythemia 3 9.4
2157 infantile cerebellar-retinal degeneration 9.4
2158 peripartum cardiomyopathy 9.4
2159 pontine tegmental cap dysplasia 9.4