CORD2
MCID: CNR004
MIFTS: 63

Cone-Rod Dystrophy 2 (CORD2)

Categories: Eye diseases, Genetic diseases, Neuronal diseases, Rare diseases

Aliases & Classifications for Cone-Rod Dystrophy 2

MalaCards integrated aliases for Cone-Rod Dystrophy 2:

Name: Cone-Rod Dystrophy 2 58 12 54 76 30 6 15 39 74
Cone-Rod Dystrophy 58 39 12 77 54 26 30 13 56 6 15
Cord2 58 12 54 76
Cone-Rod Retinal Dystrophy 2 12 54 76
Cone-Rod Retinal Dystrophy 58 12 26
Rcrd2 58 12 54
Crd2 12 54 76
Cone-Rod Retinal Dystrophy-2 58 13
Retinal Cone-Rod Dystrophy 2 12 54
Retinal Cone-Rod Dystrophy 58 26
Cord 58 26
Crd 58 26
Cone-Rod Retinal Dystrophy; Crd; Crd2 58
Retinal Cone-Rod Dystrophy; Rcrd2 58
Progressive Cone-Rod Dystrophy 74
Dystrophy, Cone-Rod, Type 2 41
Tapetoretinal Degeneration 26
Cone-Rod Dystrophy; Cord 58
Retinitis Pigmentosa 2 74
Cone-Rod Degeneration 26
Retinitis Pigmentosa 74

Characteristics:

OMIM:

58
Inheritance:
autosomal dominant (19q13.1-q13.2)


HPO:

33
cone-rod dystrophy 2:
Inheritance autosomal dominant inheritance


Classifications:



Summaries for Cone-Rod Dystrophy 2

NIH Rare Diseases : 54 Cone-rod dystrophy (CRD) is a group of inheritedeye disorders that affect the light sensitive cells of the retina called the cones and rods. People with this condition experience vision loss over time as the cones and rods deteriorate. Initial signs and symptoms that usually occur in childhood may include decreased sharpness of vision (visual acuity) and abnormal sensitivity to light (photophobia). These signs are usually followed by blind spots in the central field of vision (scotomas), loss of color perception, and loss of peripheral vision. Most individuals with this condition are legally blind by mid adulthood. There are over 30 types of CRD caused by mutations in several different genes that can be inherited in many different ways including autosomal recessive, autosomal dominant, X-linked or mitochondrial patterns. CRDs are usually non-syndromic, but they may also be part of several syndromes. There is no cure for CRD; however, there may be ways to slow the disease process. Depending on the underlying cause of CRD and other associated symptoms, research may be ongoing to try to identify an effective treatment.

MalaCards based summary : Cone-Rod Dystrophy 2, also known as cone-rod dystrophy, is related to cone-rod dystrophy 7 and cone-rod dystrophy 6. An important gene associated with Cone-Rod Dystrophy 2 is CRX (Cone-Rod Homeobox), and among its related pathways/superpathways are Phototransduction and Metabolism of fat-soluble vitamins. The drugs Antioxidants and Anesthetics have been mentioned in the context of this disorder. Affiliated tissues include Eye and Eye, and related phenotypes are reduced visual acuity and constriction of peripheral visual field

Disease Ontology : 12 A retinal degeneration that characterized by progressive deterioration of the cone and rod photoreceptor cells.

Genetics Home Reference : 26 Cone-rod dystrophy is a group of related eye disorders that causes vision loss, which becomes more severe over time. These disorders affect the retina, which is the layer of light-sensitive tissue at the back of the eye. In people with cone-rod dystrophy, vision loss occurs as the light-sensing cells of the retina gradually deteriorate.

OMIM : 58 Cone-rod dystrophy (CORD) characteristically leads to early impairment of vision. An initial loss of color vision and of visual acuity is followed by nyctalopia (night blindness) and loss of peripheral visual fields. In extreme cases, these progressive symptoms are accompanied by widespread, advancing retinal pigmentation and chorioretinal atrophy of the central and peripheral retina (Moore, 1992). In many families, perhaps a majority, central and peripheral chorioretinal atrophy is not found (Tzekov, 1998). (120970)

UniProtKB/Swiss-Prot : 76 Cone-rod dystrophy 2: An inherited retinal dystrophy characterized by retinal pigment deposits visible on fundus examination, predominantly in the macular region, and initial loss of cone photoreceptors followed by rod degeneration. This leads to decreased visual acuity and sensitivity in the central visual field, followed by loss of peripheral vision. Severe loss of vision occurs earlier than in retinitis pigmentosa, due to cone photoreceptors degenerating at a higher rate than rod photoreceptors.

Wikipedia : 77 A cone dystrophy is an inherited ocular disorder characterized by the loss of cone cells, the... more...

Related Diseases for Cone-Rod Dystrophy 2

Diseases in the Cone-Rod Dystrophy 6 family:

Cone-Rod Dystrophy 2 Cone-Rod Dystrophy 1
Cone-Rod Dystrophy 5 Cone-Rod Dystrophy 7
Cone-Rod Dystrophy 3 Cone-Rod Dystrophy 8
Cone-Rod Dystrophy 13 Cone-Rod Dystrophy 10
Cone-Rod Dystrophy 11 Cone-Rod Dystrophy 12
Cone-Rod Dystrophy 9 Cone-Rod Dystrophy 15
Cone-Rod Dystrophy 16 Cone-Rod Dystrophy 17
Cone-Rod Dystrophy 18 Cone-Rod Dystrophy 19
Cone-Rod Dystrophy 20 Cone-Rod Dystrophy 21

Diseases related to Cone-Rod Dystrophy 2 via text searches within MalaCards or GeneCards Suite gene sharing:

(showing 2263, show less)
# Related Disease Score Top Affiliating Genes
1 cone-rod dystrophy 7 35.2 ABCA4 RIMS1
2 cone-rod dystrophy 6 35.1 GUCA1A GUCY2D RPGR
3 cone-rod dystrophy 9 35.1 ABCA4 CRX GUCY2D RPGRIP1
4 cone-rod dystrophy 12 35.1 CERKL PROM1
5 cone-rod dystrophy 8 35.0 ABCA4 CORD8 CRX GUCY2D RPGRIP1
6 cone-rod dystrophy 1 34.9 CORD1 RPGRIP1
7 leber congenital amaurosis 4 34.1 AIPL1 CRX GUCY2D
8 retinitis pigmentosa 3 33.8 ABCA4 RPGR RPGRIP1
9 leber congenital amaurosis 1 33.2 GUCA1A GUCY2D TULP1
10 retinitis pigmentosa 32.8 ABCA4 AIPL1 CERKL CRX FAM161A GUCA1A
11 retinitis 31.7 CERKL FAM161A PRPH2 RHO RPGR RPGRIP1
12 stargardt disease 31.5 ABCA4 PROM1 PRPH2 RHO RPGR
13 stargardt disease 1 31.3 ABCA4 CRX RHO
14 fundus dystrophy 31.1 ABCA4 AIPL1 CERKL CRX GUCA1A GUCY2D
15 retinitis pigmentosa 19 30.9 ABCA4 RHO
16 retinitis pigmentosa 1 30.9 PRPH2 RHO
17 cone dystrophy 30.9 GUCA1A RHO RPGR
18 stargardt macular degeneration 30.9 ABCA4 PRPH2 RHO RIMS1
19 leber congenital amaurosis 30.9 ABCA4 AIPL1 CRX GUCA1A GUCY2D NR2E3
20 retinal degeneration 30.7 ABCA4 AIPL1 CRX GUCA1A GUCY2D NR2E3
21 enhanced s-cone syndrome 29.8 AIPL1 CRX NR2E3
22 yemenite deaf-blind hypopigmentation syndrome 29.6 ABCA4 AIPL1 GUCY2D RHO RPGR
23 retinal disease 29.3 ABCA4 AIPL1 CRX GUCA1A GUCY2D PRPH2
24 spondylometaphyseal dysplasia with cone-rod dystrophy 13.0
25 cone-rod dystrophy, x-linked, 1 13.0
26 cone-rod dystrophy, x-linked, 3 12.9
27 cone-rod dystrophy 3 12.9
28 cone-rod dystrophy and hearing loss 1 12.9
29 cone-rod dystrophy 18 12.9
30 cone-rod dystrophy 20 12.9
31 cone-rod dystrophy 13 12.9
32 cone-rod dystrophy 15 12.9
33 cone-rod dystrophy and hearing loss 2 12.8
34 cone-rod dystrophy 5 12.8
35 cone-rod dystrophy 10 12.8
36 cone-rod dystrophy 19 12.8
37 cone-rod dystrophy 11 12.8
38 cone-rod dystrophy 21 12.8
39 cone-rod dystrophy 17 12.7
40 spinal cord injury 12.7
41 spinal cord disease 12.5
42 leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation 12.5
43 jalili syndrome 12.5
44 cerebellar hypoplasia tapetoretinal degeneration 12.5
45 tethered spinal cord syndrome 12.5
46 sex cord-gonadal stromal tumor 12.4
47 hypomyelination with brainstem and spinal cord involvement and leg spasticity 12.4
48 mental retardation, severe, with spasticity and pigmentary tapetoretinal degeneration 12.4
49 cone dystrophy 3 12.4
50 tethered cord syndrome 12.4
51 distal myopathy with vocal cord weakness 12.4
52 central cord syndrome 12.3
53 split spinal cord malformation 12.3
54 spinal cord ependymoma 12.3
55 spinal cord glioma 12.3
56 spinal cord infarction 12.3
57 spinal cord lymphoma 12.3
58 tapetoretinal degeneration with ataxia 12.3
59 charcot-marie-tooth disease, axonal, with vocal cord paresis, autosomal recessive 12.3
60 testicular sex cord-stromal neoplasm 12.3
61 umbilical cord ulceration and intestinal atresia 12.3
62 ovarian sex cord tumor with annular tubules 12.3
63 spinal cord lipoma 12.3
64 lipoma of spermatic cord 12.3
65 spinal cord dermoid cyst 12.3
66 central cervical cord syndrome 12.3
67 ovarian sex-cord stromal tumor 12.2
68 spinal cancer 12.2
69 spinal cord astrocytoma 12.2
70 spermatic cord cancer 12.2
71 mixed germ cell-sex cord neoplasm 12.2
72 spinal cord melanoma 12.2
73 spinal cord oligodendroglioma 12.1
74 spinal cord primitive neuroectodermal neoplasm 12.1
75 spinal cord sarcoma 12.1
76 spinal cord neuroblastoma 12.1
77 primary tethered cord syndrome 12.1
78 spinal cord intramedullary teratoma 12.1
79 newfoundland rod-cone dystrophy 12.1
80 idiopathic spinal cord herniation 12.0
81 adult spinal cord glioblastoma multiforme 12.0
82 childhood spinal cord tumor 12.0
83 chylomicron retention disease 12.0
84 vocal cord paralysis and ptosis 12.0
85 spinal canal and spinal cord meningioma 12.0
86 thoracic spinal canal and spinal cord meningioma 12.0
87 lumbar spinal canal and spinal cord meningioma 12.0
88 multiple spinal canal and spinal cord meningioma 12.0
89 adult spinal cord ependymoma 12.0
90 cervical spinal canal and spinal cord meningioma 12.0
91 sacral spinal canal and spinal cord meningioma 12.0
92 congenital laryngeal palsy 11.9
93 vascular helix of umbilical cord 11.9
94 vocal cord scarring 11.9
95 sex cord-stromal benign neoplasm 11.9
96 ovarian sex cord-stromal benign neoplasm 11.9
97 testicular sex cord-stromal benign neoplasm 11.9
98 neurofibroma of spinal cord 11.9
99 testicular torsion 11.9
100 neuronopathy, distal hereditary motor, type viia 11.8
101 limb-body wall complex 11.8
102 diastematomyelia 11.8
103 spondylometaphyseal dysplasia, axial 11.8
104 brown-sequard syndrome 11.7
105 spondylosis 11.7
106 spinal meningioma 11.7
107 hypotrichosis, congenital, with juvenile macular dystrophy 11.7
108 cone-rod dystrophy, x-linked, 2 11.6
109 amyotrophic lateral sclerosis 21 11.6
110 vascular disease 11.6
111 bietti crystalline corneoretinal dystrophy 11.6
112 laryngeal abductor paralysis 11.6
113 syringomyelia 11.6
114 transverse myelitis 11.5
115 hydromyelia 11.5
116 hemangioblastoma 11.5
117 neuronopathy, distal hereditary motor, type viib 11.5
118 charcot-marie-tooth disease, axonal, type 2k 11.5
119 neural tube defects 11.5
120 neuromyelitis optica 11.5
121 arachnoid cysts 11.5
122 amyotrophic lateral sclerosis 1 11.4
123 cleft lip-retinopathy syndrome 11.4
124 chiari malformation type i 11.4
125 tucker syndrome 11.4
126 myelomeningocele 11.4
127 multiple sclerosis 11.4
128 cone-rod dystrophy 16 11.4
129 chiari malformation type ii 11.4
130 chiari malformation 11.4
131 arteriovenous malformation 11.3
132 myelitis 11.3
133 brachial plexus lesion 11.3
134 cortisone reductase deficiency 1 11.3
135 cortisone reductase deficiency 2 11.3
136 meningitis 11.3
137 cerebral cavernous malformations 11.3
138 acute flaccid myelitis 11.3
139 alstrom syndrome 11.3
140 bardet-biedl syndrome 1 11.3
141 blue cone monochromacy 11.3
142 leber congenital amaurosis 3 11.3
143 leber congenital amaurosis 10 11.3
144 cone dystrophy 4 11.3
145 bardet-biedl syndrome 11.3
146 syringohydromyelia 11.3
147 acute disseminated encephalomyelitis 11.3
148 cobb syndrome 11.3
149 spasticity 11.3
150 astrocytoma 11.3
151 fibrocartilaginous embolism 11.3
152 abdominal wall defect 11.3
153 cerebellar hypoplasia 11.3
154 oculorenocerebellar syndrome 11.3
155 anencephaly 11.2
156 spinal muscular atrophy, type i 11.2
157 laryngeal adductor paralysis 11.2
158 distal hereditary motor neuropathy type 7 11.2
159 spinal intradural arachnoid cysts 11.2
160 cerebellar degeneration 11.2
161 foix-alajouanine syndrome 11.2
162 spinal stenosis 11.2
163 epidural abscess 11.2
164 arachnoiditis 11.2
165 peripheral nervous system disease 11.2
166 meningioma, familial 11.2
167 respiratory failure 11.2
168 cavernous malformation 11.2
169 charcot-marie-tooth disease 11.2
170 cavernous hemangioma 11.2
171 ossification of the posterior longitudinal ligament of spine 11.2
172 cauda equina syndrome 11.2
173 spinocerebellar ataxia 1 11.2
174 chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids 11.2
175 paraplegia 11.2
176 glioma susceptibility 1 11.1
177 spinal muscular atrophy 11.1
178 meningocele 11.1
179 funisitis 11.1
180 neurosarcoidosis 11.1
181 von hippel-lindau syndrome 11.1
182 congenital hydrocephalus 11.1
183 varicocele 11.1
184 adrenoleukodystrophy 11.1
185 patau syndrome 11.1
186 spinal shock 11.1
187 guillain-barre syndrome 11.1
188 metachromatic leukodystrophy 11.1
189 anaplastic ependymoma 11.1
190 pilocytic astrocytoma 11.1
191 ependymoma 11.1
192 neuroblastoma 1 11.1
193 gonadoblastoma 11.1
194 anterior spinal artery syndrome 11.1
195 amyotrophy, monomelic 11.1
196 tabes dorsalis 11.1
197 laryngitis 11.1
198 afibrinogenemia, congenital 11.1
199 hereditary spastic paraplegia 11.1
200 marfan syndrome 11.1
201 stiff-person syndrome 11.1
202 schizencephaly 11.1
203 pelizaeus-merzbacher disease 11.1
204 autonomic neuropathy 11.1
205 intracranial hypotension 11.1
206 cerebral cavernous malformation, familial 11.1
207 hypotonia 11.1
208 spontaneous intracranial hypotension 11.1
209 goiter, multinodular, cystic renal disease, and digital anomalies 11.1
210 refsum disease, classic 11.1
211 daneman davy mancer syndrome 11.1
212 acute cystitis 11.1
213 glioma 11.1
214 hematopoietic stem cell transplantation 11.1
215 neurogenic bowel 11.0
216 motor neuron disease 11.0
217 cerebral palsy 11.0
218 beta-thalassemia 11.0
219 hydrocephalus 11.0
220 pure autonomic failure 11.0
221 encephalitis 11.0
222 paresthesia 11.0
223 multiple system atrophy 1 11.0
224 intracranial cysts 11.0
225 mononeuropathy 11.0
226 myoclonus 11.0
227 klippel-feil syndrome 11.0
228 leukodystrophy 11.0
229 achondroplasia 11.0
230 tetanus 11.0
231 tropical spastic paraparesis 11.0
232 gastroschisis 11.0
233 myeloma, multiple 11.0
234 adrenomyeloneuropathy 11.0
235 krabbe disease 11.0
236 gangliocytoma 11.0
237 caudal regression sequence 11.0
238 west nile virus 11.0
239 rabies 11.0
240 hhv-6 encephalitis 11.0
241 tremor 11.0
242 sensory peripheral neuropathy 11.0
243 myxopapillary ependymoma 11.0
244 proximal spinal muscular atrophy 11.0
245 burkitt lymphoma 11.0
246 creutzfeldt-jakob disease 11.0
247 sacral defect with anterior meningocele 11.0
248 spina bifida occulta 11.0
249 grade iii astrocytoma 11.0
250 bacterial meningitis 11.0
251 spinal and bulbar muscular atrophy, x-linked 1 11.0
252 buerger disease 11.0
253 leigh syndrome 11.0
254 tetanus neonatorum 11.0
255 primary angiitis of the central nervous system 11.0
256 hypertonia 11.0
257 cerebrotendinous xanthomatosis 11.0
258 duodenal atresia 11.0
259 testicular seminoma 11.0
260 melanosis, neurocutaneous 11.0
261 movement disease 11.0
262 distal hereditary motor neuropathies 11.0
263 neurosyphilis 11.0
264 syphilitic myelopathy 11.0
265 ovarian fibroma 11.0
266 machado-joseph disease 11.0
267 friedreich ataxia 1 11.0
268 omenn syndrome 11.0
269 mucopolysaccharidosis iii 11.0
270 neonatal stroke 11.0
271 adenoid cystic carcinoma 11.0
272 atypical teratoid rhabdoid tumor 11.0
273 glomus vagale tumor 11.0
274 iniencephaly 11.0
275 primary central nervous system lymphoma 11.0
276 neurofibromatosis, type ii 10.9
277 adie pupil 10.9
278 neuropathy, hereditary, with liability to pressure palsies 10.9
279 temporal arteritis 10.9
280 joubert syndrome 1 10.9
281 hydrocephalus, normal-pressure 10.9
282 familial mediterranean fever 10.9
283 papilloma of choroid plexus 10.9
284 porphyria, congenital erythropoietic 10.9
285 wernicke-korsakoff syndrome 10.9
286 leukoencephalopathy with vanishing white matter 10.9
287 hereditary motor and sensory neuropathy, type iic 10.9
288 acute hemorrhagic leukoencephalitis 10.9
289 leukocyte adhesion deficiency, type iii 10.9
290 aicardi-goutieres syndrome 10.9
291 syphilitic meningitis 10.9
292 neuroschistosomiasis 10.9
293 factor xiii deficiency 10.9
294 brain stem glioma 10.9
295 essential tremor 10.9
296 progressive bulbar palsy 10.9
297 dandy-walker complex 10.9
298 idiopathic hypertrophic pachymeningitis 10.9
299 tarlov cysts 10.9
300 swallowing disorders 10.9
301 midline cervical cleft 10.9
302 apnea of prematurity 10.9
303 behcet syndrome 10.9
304 central pain syndrome 10.9
305 brain and spinal tumors 10.9
306 charcot-marie-tooth disease type 2g 10.9
307 sandhoff disease 10.9
308 tay-sachs disease 10.9
309 primary lateral sclerosis, juvenile 10.9
310 gm1 gangliosidosis 10.9
311 vascular erectile tumor 10.9
312 congenital vascular cavernous malformations 10.9
313 familial hemangioma 10.9
314 amyloidosis, hereditary, transthyretin-related 10.8
315 laryngeal web, familial 10.8
316 spinal muscular atrophy, lower extremity-predominant, 1, autosomal dominant 10.8
317 omphalocele, autosomal 10.8
318 spinal muscular atrophy, late-onset, finkel type 10.8
319 spinocerebellar ataxia 2 10.8
320 syringomyelia, noncommunicating isolated 10.8
321 proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome 10.8
322 spinal muscular atrophy, type iii 10.8
323 spinal muscular atrophy, type ii 10.8
324 gm2-gangliosidosis, ab variant 10.8
325 spastic paraplegia 20, autosomal recessive 10.8
326 pontocerebellar hypoplasia, type 2a 10.8
327 spastic paraplegia 2, x-linked 10.8
328 spinocerebellar ataxia 5 10.8
329 athabaskan brainstem dysgenesis syndrome 10.8
330 spinal muscular atrophy, distal, autosomal recessive, 1 10.8
331 spinocerebellar ataxia 13 10.8
332 pontocerebellar hypoplasia, type 2b 10.8
333 pontocerebellar hypoplasia, type 2c 10.8
334 viral meningitis 10.8
335 aseptic meningitis 10.8
336 central nervous system disease 10.8
337 cerebral ventricle cancer 10.8
338 croup 10.8
339 giant axonal neuropathy 10.8
340 cerebro-oculo-facio-skeletal syndrome 10.8
341 chronic hiccups 10.8
342 diffuse intrinsic pontine glioma 10.8
343 floppy infant syndrome 10.8
344 ischemia 10.7
345 frontotemporal dementia and/or amyotrophic lateral sclerosis 1 10.6
346 spinocerebellar ataxia 31 10.6
347 cerebral amyloid angiopathy, itm2b-related, 2 10.6
348 charcot-marie-tooth disease, axonal, type 2a1 10.6
349 charcot-marie-tooth disease and deafness 10.6
350 lateral meningocele syndrome 10.6
351 multiple endocrine neoplasia, type i 10.6
352 spinocerebellar ataxia 34 10.6
353 neuromyotonia and axonal neuropathy, autosomal recessive 10.6
354 chromosome 8q22.1 duplication syndrome 10.6
355 neuronopathy, distal hereditary motor, type iia 10.6
356 spinocerebellar ataxia 6 10.6
357 splenogonadal fusion with limb defects and micrognathia 10.6
358 thanatophoric dysplasia, type ii 10.6
359 neuropathy, hereditary sensory and autonomic, type iia 10.6
360 amyotonia congenita 10.6
361 amyotrophic lateral sclerosis 2, juvenile 10.6
362 arthrogryposis multiplex congenita, neurogenic type 10.6
363 spinocerebellar ataxia, autosomal recessive 2 10.6
364 complement component 2 deficiency 10.6
365 dandy-walker syndrome 10.6
366 dyggve-melchior-clausen disease 10.6
367 aicardi-goutieres syndrome 1 10.6
368 gm1-gangliosidosis, type i 10.6
369 gm1-gangliosidosis, type ii 10.6
370 gm1-gangliosidosis, type iii 10.6
371 gaucher disease, type i 10.6
372 lipoid proteinosis of urbach and wiethe 10.6
373 microcephaly with cervical spine fusion anomalies 10.6
374 lethal congenital contracture syndrome 1 10.6
375 congenital disorder of glycosylation, type iic 10.6
376 spastic ataxia, charlevoix-saguenay type 10.6
377 spinal muscular atrophy, type iv 10.6
378 mitochondrial dna depletion syndrome 7 10.6
379 subaortic stenosis--short stature syndrome 10.6
380 spinal muscular atrophy, distal, x-linked 3 10.6
381 toe syndactyly, telecanthus, and anogenital and renal malformations 10.6
382 amyotrophic lateral sclerosis 15 with or without frontotemporal dementia 10.6
383 neural tube defects, x-linked 10.6
384 spinal muscular atrophy, x-linked 2 10.6
385 spinocerebellar ataxia, x-linked 1 10.6
386 kearns-sayre syndrome 10.6
387 mesomelia-synostoses syndrome 10.6
388 neuronopathy, distal hereditary motor, type va 10.6
389 amyotrophic lateral sclerosis 5, juvenile 10.6
390 amyotrophic lateral sclerosis 4, juvenile 10.6
391 histiocytosis-lymphadenopathy plus syndrome 10.6
392 spinocerebellar ataxia 10 10.6
393 congenital cataracts, facial dysmorphism, and neuropathy 10.6
394 spinocerebellar ataxia 12 10.6
395 cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 10.6
396 spinocerebellar ataxia 11 10.6
397 charcot-marie-tooth disease, type 4b2 10.6
398 spinocerebellar ataxia 14 10.6
399 radioulnar synostosis with amegakaryocytic thrombocytopenia 1 10.6
400 spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2 10.6
401 amyotrophic lateral sclerosis 3 10.6
402 spinocerebellar ataxia 15 10.6
403 lipodystrophy, familial partial, type 7 10.6
404 hurler-scheie syndrome 10.6
405 cinca syndrome 10.6
406 spinocerebellar ataxia 17 10.6
407 spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1 10.6
408 spastic paraplegia 7, autosomal recessive 10.6
409 spinocerebellar ataxia, autosomal recessive 4 10.6
410 smith-mccort dysplasia 1 10.6
411 spinocerebellar ataxia 19 10.6
412 spinocerebellar ataxia 21 10.6
413 pontocerebellar hypoplasia, type 1a 10.6
414 lethal congenital contracture syndrome 2 10.6
415 amyotrophic lateral sclerosis 6 with or without frontotemporal dementia 10.6
416 amyotrophic lateral sclerosis 8 10.6
417 neuronopathy, distal hereditary motor, type iib 10.6
418 neuropathy, hereditary sensory and autonomic, type v 10.6
419 spinocerebellar ataxia 20 10.6
420 spinocerebellar ataxia 8 10.6
421 leukodystrophy, hypomyelinating, 2 10.6
422 ataxia, sensory, 1, autosomal dominant 10.6
423 posterior column ataxia with retinitis pigmentosa 10.6
424 myopathy, myofibrillar, 3 10.6
425 charcot-marie-tooth disease, axonal, autosomal dominant, type 2a2a 10.6
426 spinocerebellar ataxia, autosomal recessive 7 10.6
427 spinocerebellar ataxia 26 10.6
428 spinocerebellar ataxia 27 10.6
429 aicardi-goutieres syndrome 2 10.6
430 spinocerebellar ataxia 23 10.6
431 spinocerebellar ataxia 28 10.6
432 aicardi-goutieres syndrome 3 10.6
433 aicardi-goutieres syndrome 4 10.6
434 spinocerebellar ataxia, autosomal recessive 8 10.6
435 spinal muscular atrophy, distal, autosomal recessive, 4 10.6
436 congenital arthrogryposis with anterior horn cell disease 10.6
437 amyotrophic lateral sclerosis 9 10.6
438 amyotrophic lateral sclerosis 10 with or without frontotemporal dementia 10.6
439 amyotrophic lateral sclerosis 11 10.6
440 aicardi-goutieres syndrome 5 10.6
441 neuronopathy, distal hereditary motor, type iic 10.6
442 amyotrophic lateral sclerosis 12 10.6
443 odontoid hypoplasia 10.6
444 prothrombin deficiency, congenital 10.6
445 spinocerebellar ataxia, autosomal recessive 10 10.6
446 spinocerebellar ataxia 35 10.6
447 amyotrophic lateral sclerosis 14 with or without frontotemporal dementia 10.6
448 spinocerebellar ataxia 36 10.6
449 spinocerebellar ataxia, autosomal recessive 11 10.6
450 spinocerebellar ataxia, autosomal recessive 12 10.6
451 amyotrophic lateral sclerosis 16, juvenile 10.6
452 neuronopathy, distal hereditary motor, type vb 10.6
453 amyotrophic lateral sclerosis 18 10.6
454 spinocerebellar ataxia, autosomal recessive 13 10.6
455 multiple mitochondrial dysfunctions syndrome 3 10.6
456 spinocerebellar ataxia, autosomal recessive 14 10.6
457 amyotrophic lateral sclerosis 20 10.6
458 amyotrophic lateral sclerosis 19 10.6
459 spinocerebellar ataxia, autosomal recessive 15 10.6
460 spinocerebellar ataxia, autosomal recessive 16 10.6
461 frontotemporal dementia and/or amyotrophic lateral sclerosis 2 10.6
462 spinocerebellar ataxia 37 10.6
463 spinocerebellar ataxia 38 10.6
464 spinocerebellar ataxia 40 10.6
465 spinocerebellar ataxia, autosomal recessive 17 10.6
466 spinocerebellar ataxia, autosomal recessive 18 10.6
467 amyotrophic lateral sclerosis 22 with or without frontotemporal dementia 10.6
468 spinocerebellar ataxia, autosomal recessive 20 10.6
469 multiple mitochondrial dysfunctions syndrome 4 10.6
470 spinocerebellar ataxia 41 10.6
471 frontotemporal dementia and/or amyotrophic lateral sclerosis 3 10.6
472 frontotemporal dementia and/or amyotrophic lateral sclerosis 4 10.6
473 spinocerebellar ataxia, autosomal recessive 21 10.6
474 spinocerebellar ataxia 42 10.6
475 spasticity, childhood-onset, with hyperglycinemia 10.6
476 spinocerebellar ataxia, autosomal recessive 22 10.6
477 spinocerebellar ataxia, autosomal recessive 23 10.6
478 spinocerebellar ataxia 43 10.6
479 spinocerebellar ataxia, autosomal recessive 24 10.6
480 spinocerebellar ataxia, autosomal recessive 25 10.6
481 spinocerebellar ataxia, autosomal recessive 26 10.6
482 spinocerebellar ataxia 44 10.6
483 spinocerebellar ataxia 45 10.6
484 spinocerebellar ataxia 46 10.6
485 amyotrophic lateral sclerosis 23 10.6
486 amyotrophic lateral sclerosis 24 10.6
487 amyotrophic lateral sclerosis 25 10.6
488 spinocerebellar ataxia 47 10.6
489 leukodystrophy, hypomyelinating, 17 10.6
490 spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits 10.6
491 spinocerebellar ataxia 48 10.6
492 basal ganglia calcification, idiopathic, 7, autosomal recessive 10.6
493 brain meningioma 10.6
494 childhood-onset cerebral x-linked adrenoleukodystrophy 10.6
495 craniorachischisis 10.6
496 autoimmune peripheral neuropathy 10.6
497 baylisascariasis 10.6
498 meningovascular neurosyphilis 10.6
499 spinal polio 10.6
500 bulbospinal polio 10.6
501 malignant leydig cell tumor 10.6
502 malignant sertoli cell tumor 10.6
503 malignant sertoli-leydig cell tumor 10.6
504 spasmodic dystonia 10.6
505 sublingual gland adenoid cystic carcinoma 10.6
506 parotid gland adenoid cystic carcinoma 10.6
507 ovarian clear cell carcinoma 10.6
508 lymph node adenoid cystic carcinoma 10.6
509 haemophilus meningitis 10.6
510 malignant epithelioid hemangioendothelioma 10.6
511 fungal meningitis 10.6
512 juvenile spinal muscular atrophy 10.6
513 central nervous system tuberculosis 10.6
514 mononeuritis multiplex 10.6
515 transient cerebral ischemia 10.6
516 cerebellar disease 10.6
517 thoracic outlet syndrome 10.6
518 brachial plexus neuropathy 10.6
519 childhood brain stem glioma 10.6
520 breast epithelioid hemangioma 10.6
521 adult myxoid chondrosarcoma 10.6
522 cervical large cell neuroendocrine carcinoma 10.6
523 childhood brain meningioma 10.6
524 tertiary neurosyphilis 10.6
525 autosomal dominant leukodystrophy with autonomic disease 10.6
526 grin2b-related neurodevelopmental disorder 10.6
527 spastic paraplegia 11 10.6
528 brain tumor, childhood 10.6
529 choroid plexus cyst 10.6
530 cockayne syndrome type ii 10.6
531 desmoplastic small round cell tumor 10.6
532 extracranial arteriovenous malformation 10.6
533 gemignani syndrome 10.6
534 giant congenital nevus 10.6
535 granulosa cell tumor of the ovary 10.6
536 gynandroblastoma 10.6
537 handl syndrome 10.6
538 hemimegalencephaly 10.6
539 hypertrophic olivary degeneration 10.6
540 infantile-onset ascending hereditary spastic paralysis 10.6
541 limb-girdle muscular dystrophy type 1a 10.6
542 meningococcal infection 10.6
543 meningoencephalocele 10.6
544 mollaret meningitis 10.6
545 neisseria meningitidis infection 10.6
546 painful legs and moving toes syndrome 10.6
547 paraneoplastic neurologic disorders 10.6
548 pontocerebellar hypoplasia type 1 10.6
549 riboflavin transporter deficiency 10.6
550 spastic paraplegia 15 10.6
551 spastic paraplegia 5a 10.6
552 subacute cerebellar degeneration 10.6
553 thyrotoxic periodic paralysis 10.6
554 urachal cyst 10.6
555 complement component 8 deficiency 10.6
556 distal hereditary motor neuropathy, type ii 10.6
557 distal hereditary motor neuropathy, type v 10.6
558 lissencephaly with cerebellar hypoplasia 10.6
559 aids - neurological complications 10.6
560 immune-mediated encephalomyelitis 10.6
561 infantile hypotonia 10.6
562 korsakoff's amnesic syndrome 10.6
563 megalencephaly 10.6
564 meningitis and encephalitis 10.6
565 mini stroke 10.6
566 o'sullivan-mcleod syndrome 10.6
567 postinfectious encephalomyelitis 10.6
568 progressive locomotor ataxia 10.6
569 shaken baby syndrome 10.6
570 syphilitic spinal sclerosis 10.6
571 vasculitis syndromes of the central and peripheral nervous systems 10.6
572 cerebral beriberi 10.6
573 erb's palsy 10.6
574 amelogenesis imperfecta 10.6
575 spondyloepimetaphyseal dysplasia, strudwick type 10.6
576 macular dystrophy, concentric annular 10.6 ABCA4 CRX
577 eye degenerative disease 10.5 GUCA1A GUCY2D PRPH2
578 peripheral retinal degeneration 10.5 PRPH2 RPGR
579 leukemia 10.5
580 hereditary retinal dystrophy 10.5 GUCY2D RHO
581 allergic encephalomyelitis 10.5
582 choroidal dystrophy, central areolar, 1 10.5 GUCA1A GUCY2D PRPH2 RIMS1
583 prolonged electroretinal response suppression 10.5 ABCA4 CRX GUCY2D PROM1 PRPH2
584 choroid disease 10.5 RHO RPGR
585 laurence-moon syndrome 10.5 RPGR RPGRIP1
586 leber congenital amaurosis 9 10.4 AIPL1 CRX GUCY2D RPGRIP1 TULP1
587 cancer-associated retinopathy 10.4 RHO TULP1
588 vascular myelopathy 10.4
589 achromatopsia 3 10.4 AIPL1 CRX GUCY2D RPGRIP1 TULP1
590 lateral sclerosis 10.4
591 corneal dystrophy 10.4
592 diencephalic syndrome 10.4
593 secondary syringomyelia 10.4
594 idiopathic syringomyelia 10.4
595 primary syringomyelia 10.4
596 hereditary choroidal atrophy 10.4 AIPL1 GUCA1A GUCY2D PROM1 PRPH2 RIMS1
597 partial central choroid dystrophy 10.4 AIPL1 GUCA1A GUCY2D PROM1 PRPH2 RIMS1
598 red-green color blindness 10.4 ABCA4 RHO
599 neurogenic bladder 10.4
600 congenital stationary night blindness 10.4 ABCA4 AIPL1 RHO
601 retinitis pigmentosa 7 10.4 PRPH2 RHO
602 lymphoma 10.4
603 pain - chronic 10.4
604 benign ependymoma 10.3
605 decubitus ulcer 10.3
606 liposarcoma 10.3
607 tritanopia 10.3 GUCY2D RHO
608 danon disease 10.3
609 ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus 10.3
610 myopia 10.3
611 megaloblastic anemia 10.3
612 pathologic nystagmus 10.3
613 neuropathy 10.3
614 graft-versus-host disease 10.3
615 complex regional pain syndrome 10.3
616 angina pectoris 10.3
617 quadriplegia 10.3
618 pre-eclampsia 10.3
619 aortic aneurysm 10.2
620 acute leukemia 10.2
621 lipomatosis, multiple 10.2
622 scoliosis 10.2
623 pleomorphic lipoma 10.2
624 depression 10.2
625 thalassemia 10.2
626 hemangioma 10.2
627 brain injury 10.2
628 intermittent claudication 10.2
629 aplastic anemia 10.2
630 pulmonary fibrosis and/or bone marrow failure, telomere-related, 2 10.2
631 gestational diabetes 10.2
632 hypoxia 10.2
633 duane retraction syndrome 10.2
634 isolated duane retraction syndrome 10.2
635 sarcoma 10.2
636 osteochondroma 10.2
637 laryngeal abductor paralysis-intellectual disability syndrome 10.2
638 congenital cervical spinal stenosis 10.2
639 diabetes mellitus 10.2
640 teratoma 10.2
641 encephalopathy 10.2
642 usher syndrome, type iid 10.2 RHO RPGR
643 impotence 10.2
644 glioblastoma 10.2
645 neuromyelitis optica spectrum disorder 10.2
646 traumatic brain injury 10.2
647 myelodysplastic syndrome 10.1
648 bacteriuria 10.1
649 lymphocytic leukemia 10.1
650 spondyloepiphyseal dysplasia with congenital joint dislocations 10.1
651 macular degeneration, age-related, 2 10.1
652 neurofibromatosis, type i 10.1
653 neurofibromatosis, type iv, of riccardi 10.1
654 spinocerebellar ataxia 7 10.1
655 thiamine-responsive megaloblastic anemia syndrome 10.1
656 retinitis pigmentosa 2 10.1
657 mitochondrial complex v deficiency, mitochondrial type 1 10.1
658 neuropathy, ataxia, and retinitis pigmentosa 10.1
659 macular degeneration, age-related, 1 10.1
660 nephronophthisis 4 10.1
661 polyglucosan body myopathy 1 with or without immunodeficiency 10.1
662 retinal dystrophy with or without macular staphyloma 10.1
663 achromatopsia 10.1
664 alopecia 10.1
665 cataract 10.1
666 hereditary ataxia 10.1
667 keratoconus 10.1
668 sensorineural hearing loss 10.1
669 nephronophthisis 10.1
670 autosomal dominant cerebellar ataxia 10.1
671 retinal vascular disease 10.1
672 hypotrichosis 10.1
673 cleft lip 10.1
674 muscular dystrophy 10.1
675 limb-girdle muscular dystrophy 10.1
676 myotonic dystrophy 10.1
677 growth hormone deficiency 10.1
678 myotonia atrophica 10.1
679 spondylosis, cervical 10.1
680 thrombosis 10.1
681 eclampsia 10.1
682 microphthalmia 10.1
683 3-methylglutaconic aciduria, type iii 10.1
684 chorioamnionitis 10.1
685 myeloid leukemia 10.1
686 cytomegalovirus infection 10.1
687 saethre-chotzen syndrome 10.1
688 detrusor sphincter dyssynergia 10.1
689 leukemia, acute lymphoblastic 10.1
690 limb ischemia 10.1
691 dermatitis 10.1
692 glioblastoma multiforme 10.1
693 histiocytoma 10.1
694 allergic hypersensitivity disease 10.1
695 malignant fibroxanthoma 10.1
696 fibrous histiocytoma 10.1
697 muscular atrophy 10.1
698 wallerian degeneration 10.1
699 bone cancer 10.1
700 ganglioglioma 10.1
701 trichomegaly 10.1
702 cohen syndrome 10.1
703 retinopathy, pigmentary, and mental retardation 10.1
704 senior-loken syndrome 4 10.1
705 retinitis pigmentosa 54 10.1
706 oligomeganephronia 10.1
707 albinism 10.1
708 juvenile nephronophthisis 10.1
709 arthritis 10.1
710 hepatitis 10.1
711 leiomyosarcoma 10.1
712 undifferentiated pleomorphic sarcoma 10.1
713 insulin-like growth factor i 10.1
714 leukemia, acute myeloid 10.1
715 ige responsiveness, atopic 10.0
716 paraganglioma 10.0
717 infertility 10.0
718 acute graft versus host disease 10.0
719 laryngostenosis 10.0
720 lumbosacral plexus lesion 10.0
721 malignant neoplasm of acoustic nerve 10.0
722 central nervous system cancer 10.0
723 laryngeal disease 10.0
724 isolated amyelia 10.0
725 familial syringomyelia 10.0
726 paratesticular adenocarcinoma 10.0
727 aging 10.0
728 anxiety 10.0
729 arteriovenous fistula 10.0
730 sexual disorder 10.0
731 melanoma 10.0
732 adenocarcinoma 10.0
733 oligodendroglioma 10.0
734 germinoma 10.0
735 subependymoma 10.0
736 peutz-jeghers syndrome 10.0
737 restless legs syndrome 10.0
738 schistosomiasis 10.0
739 neurofibroma 10.0
740 hereditary multiple osteochondromas 10.0
741 spastic paraparesis 10.0
742 peripheral vascular disease 10.0
743 hereditary multiple exostoses 10.0
744 asthma 10.0
745 colitis 10.0
746 osteomyelitis 10.0
747 poliomyelitis 10.0
748 neonatal hypoxic and ischemic brain injury 10.0
749 myocardial infarction 10.0
750 inguinal hernia 10.0
751 bilirubin metabolic disorder 10.0
752 histiocytosis 10.0
753 systemic lupus erythematosus 10.0
754 spondylocarpotarsal synostosis syndrome 10.0
755 deficiency anemia 10.0
756 bronchopulmonary dysplasia 10.0
757 vitamin b12 deficiency 10.0
758 hypothyroidism 10.0
759 acute respiratory distress syndrome 10.0
760 chronic enteropathy associated with slco2a1 gene 10.0
761 hemangiopericytoma, malignant 10.0
762 secretory meningioma 10.0
763 combined t cell and b cell immunodeficiency 10.0
764 herpes simplex 10.0
765 cytokine deficiency 10.0
766 breast cancer 10.0
767 mucopolysaccharidosis-plus syndrome 10.0
768 burns 10.0
769 hemophagocytic lymphohistiocytosis 10.0
770 joint disorders 10.0
771 severe combined immunodeficiency 10.0
772 polyneuropathy 10.0
773 cystitis 10.0
774 arthropathy 10.0
775 radiculopathy 10.0
776 spondylitis 10.0
777 hydrocele 10.0
778 prostate cancer 9.9
779 rheumatoid arthritis 9.9
780 myelofibrosis 9.9
781 lipomyelomeningocele 9.9
782 critical limb ischemia 9.9
783 omphalocele 9.9
784 biliary atresia 9.9
785 myeloid sarcoma 9.9
786 lupus erythematosus 9.9
787 toxoplasmosis 9.9
788 congenital cytomegalovirus 9.9
789 spondyloarthropathy 1 9.9
790 thrombophilia due to thrombin defect 9.9
791 diabetic neuropathy 9.9
792 hepatitis b 9.9
793 fibroma 9.9
794 vasculitis 9.9
795 fanconi anemia, complementation group a 9.9
796 reflex sympathetic dystrophy 9.9
797 langerhans cell histiocytosis 9.9
798 cysticercosis 9.9
799 pulmonary edema 9.9
800 algoneurodystrophy 9.9
801 capillary hemangioma 9.9
802 lipomatosis 9.9
803 chickenpox 9.9
804 ewing's family of tumors 9.9
805 neurenteric cyst 9.9
806 patent urachus 9.9
807 aortic aneurysm, familial abdominal, 1 9.9
808 epidermoid cysts 9.9
809 myelopathy, htlv-1-associated 9.9
810 sarcoidosis 1 9.9
811 neural tube defects, folate-sensitive 9.9
812 dermatitis, atopic 9.9
813 aortic aneurysm, familial thoracic 1 9.9
814 congenital hypothyroidism 9.9
815 pertussis 9.9
816 heart disease 9.9
817 central neurocytoma 9.9
818 neuritis 9.9
819 hyperostosis 9.9
820 relapsing-remitting multiple sclerosis 9.9
821 neurilemmoma 9.9
822 demyelinating disease 9.9
823 hyperglycemia 9.9
824 t-cell leukemia 9.9
825 chronic graft versus host disease 9.9
826 dysphagia 9.9
827 alzheimer disease 9.9
828 horns in sheep 9.9
829 adult t-cell leukemia 9.9
830 male infertility 9.9
831 idiopathic scoliosis 9.9
832 dermoid cyst 9.9
833 hemoglobinopathy 9.9
834 actinomycosis 9.9
835 rosai-dorfman disease 9.9
836 streptococcal group a invasive disease 9.9
837 renal cell carcinoma, nonpapillary 9.9
838 spinal arachnoiditis 9.9
839 wiskott-aldrich syndrome 9.9
840 alpha-thalassemia 9.9
841 infantile liver failure syndrome 1 9.9
842 acute lymphocytic leukemia 9.9
843 liver cirrhosis 9.9
844 lymphoproliferative syndrome 9.9
845 horner's syndrome 9.9
846 thyroid cancer 9.9
847 exostosis 9.9
848 rhabdomyosarcoma 9.9
849 mammary paget's disease 9.9
850 pneumonia 9.9
851 acquired immunodeficiency syndrome 9.9
852 polycythemia 9.9
853 rubella 9.9
854 sickle cell disease 9.9
855 bladder cancer 9.8
856 scoliosis, isolated 1 9.8
857 down syndrome 9.8
858 wilms tumor 5 9.8
859 ichthyosis prematurity syndrome 9.8
860 aspergillosis 9.8
861 wilms tumor 6 9.8
862 sclerosing cholangitis, neonatal 9.8
863 acute liver failure 9.8
864 cerebral artery occlusion 9.8
865 larynx cancer 9.8
866 testicular cancer 9.8
867 diffuse idiopathic skeletal hyperostosis 9.8
868 leukoplakia 9.8
869 headache 9.8
870 osteoporosis 9.8
871 pelger-huet anomaly 9.8
872 vesicoureteral reflux 1 9.8
873 lung cancer 9.8
874 chondrosarcoma 9.8
875 cryptorchidism, unilateral or bilateral 9.8
876 stroke, ischemic 9.8
877 prostate cancer, hereditary, 8 9.8
878 body mass index quantitative trait locus 1 9.8
879 leukemia, chronic myeloid 9.8
880 prostate cancer, hereditary, 6 9.8
881 malaria 9.8
882 chronic granulomatous disease 9.8
883 neutropenia 9.8
884 thrombocytopenia 9.8
885 cardiac arrest 9.8
886 hydronephrosis 9.8
887 endodermal sinus tumor 9.8
888 endometrial stromal sarcoma 9.8
889 aortic disease 9.8
890 kidney disease 9.8
891 adenoma 9.8
892 influenza 9.8
893 pulmonary embolism 9.8
894 tuberculous meningitis 9.8
895 postherpetic neuralgia 9.8
896 whiplash 9.8
897 diabetes mellitus, noninsulin-dependent 9.8
898 esophageal cancer 9.8
899 ovarian cancer 9.8
900 pernicious anemia 9.8
901 torticollis 9.8
902 lymphoma, hodgkin, classic 9.8
903 sickle cell anemia 9.8
904 patent ductus arteriosus 1 9.8
905 crohn's disease 9.8
906 primary progressive multiple sclerosis 9.8
907 pain agnosia 9.8
908 oligohydramnios 9.8
909 optic nerve disease 9.8
910 chondroma 9.8
911 fibrosarcoma 9.8
912 pilomyxoid astrocytoma 9.8
913 pancreatitis 9.8
914 in situ carcinoma 9.8
915 amyloidosis 9.8
916 aortic coarctation 9.8
917 hemangioendothelioma 9.8
918 spina bifida aperta 9.8
919 hepatocellular carcinoma 9.8
920 retinoblastoma 9.8
921 small cell cancer of the lung 9.8
922 congenital heart defects, hamartomas of tongue, and polysyndactyly 9.8
923 mycosis fungoides 9.8
924 polycythemia vera 9.8
925 sudden infant death syndrome 9.8
926 intervertebral disc disease 9.8
927 juvenile myelomonocytic leukemia 9.8
928 human immunodeficiency virus type 1 9.8
929 osteoarthritis 9.8
930 osteopetrosis 9.8
931 hemorrhagic cystitis 9.8
932 intestinal atresia 9.8
933 leiomyoma 9.8
934 diabetic polyneuropathy 9.8
935 diarrhea 9.8
936 lymphangioma 9.8
937 neonatal jaundice 9.8
938 epidermolysis bullosa 9.8
939 food allergy 9.8
940 plasmacytoma 9.8
941 syphilis 9.8
942 seminoma 9.8
943 dystonia 9.8
944 scrapie 9.8
945 herpes zoster 9.8
946 measles 9.8
947 priapism 9.8
948 chromosomal triplication 9.8
949 engraftment syndrome 9.8
950 hansen's disease 9.8
951 leukomalacia 9.8
952 dedifferentiated liposarcoma 9.8
953 gastroesophageal reflux 9.8
954 mesothelioma, malignant 9.8
955 wilms tumor 1 9.8
956 autism 9.8
957 enterocolitis 9.8
958 myasthenia gravis 9.8
959 sjogren syndrome 9.8
960 muscular dystrophy, duchenne type 9.8
961 ataxia and polyneuropathy, adult-onset 9.8
962 gallbladder disease 1 9.8
963 myxoid liposarcoma 9.8
964 acute myocardial infarction 9.8
965 chronic inflammatory demyelinating polyneuropathy 9.8
966 dilated cardiomyopathy 9.8
967 hemolytic anemia 9.8
968 post-transplant lymphoproliferative disease 9.8
969 tooth disease 9.8
970 chagas disease 9.8
971 goiter 9.8
972 dementia 9.8
973 periventricular leukomalacia 9.8
974 severe pre-eclampsia 9.8
975 papilledema 9.8
976 neuroma 9.8
977 constipation 9.8
978 iron metabolism disease 9.8
979 orchitis 9.8
980 benign mesothelioma 9.8
981 ganglioneuroblastoma 9.8
982 pseudohypoparathyroidism 9.8
983 polyradiculoneuropathy 9.8
984 human immunodeficiency virus infectious disease 9.8
985 thyroiditis 9.8
986 myasthenia gravis congenital 9.8
987 head injury 9.8
988 eosinophilic granuloma 9.8
989 blood group, colton system 9.7
990 klippel-trenaunay-weber syndrome 9.7
991 scheuermann disease 9.7
992 celiac disease 1 9.7
993 chondrodysplasia punctata syndrome 9.7
994 leprosy 3 9.7
995 body mass index quantitative trait locus 11 9.7
996 premature ovarian failure 1 9.7
997 body mass index quantitative trait locus 8 9.7
998 hurler syndrome 9.7
999 body mass index quantitative trait locus 10 9.7
1000 body mass index quantitative trait locus 7 9.7
1001 preterm premature rupture of the membranes 9.7
1002 body mass index quantitative trait locus 14 9.7
1003 lung cancer susceptibility 3 9.7
1004 body mass index quantitative trait locus 18 9.7
1005 body mass index quantitative trait locus 19 9.7
1006 diffuse large b-cell lymphoma 9.7
1007 fecal incontinence 9.7
1008 severe congenital neutropenia 9.7
1009 inflammatory bowel disease 9.7
1010 sparganosis 9.7
1011 rickets 9.7
1012 infant gynecomastia 9.7
1013 gynecomastia 9.7
1014 pyuria 9.7
1015 squamous cell carcinoma 9.7
1016 calcinosis 9.7
1017 giant cell tumor 9.7
1018 arteriosclerosis 9.7
1019 papilloma 9.7
1020 angiolipoma 9.7
1021 spindle cell sarcoma 9.7
1022 paget's disease of bone 9.7
1023 mucormycosis 9.7
1024 diabetes insipidus 9.7
1025 polyarteritis nodosa 9.7
1026 hemophilia 9.7
1027 chronic active epstein-barr virus infection 9.7
1028 fetal macrosomia 9.7
1029 fibromatosis 9.7
1030 fournier gangrene 9.7
1031 precocious puberty 9.7
1032 rosette-forming glioneuronal tumor 9.7
1033 dysautonomia 9.7
1034 acute transverse myelitis 9.7
1035 atlantoaxial subluxation 9.7
1036 autoimmune disease 9.7
1037 colorectal cancer 9.7
1038 factor viii deficiency 9.7
1039 huntington disease 9.7
1040 parkinson disease, late-onset 9.7
1041 spondylolisthesis 9.7
1042 thyroid cancer, nonmedullary, 2 9.7
1043 varicose veins 9.7
1044 anemia, autoimmune hemolytic 9.7
1045 sarcoma, synovial 9.7
1046 hemophilia a 9.7
1047 rett syndrome 9.7
1048 supranuclear palsy, progressive, 1 9.7
1049 acute insulin response 9.7
1050 basal cell carcinoma 1 9.7
1051 acute promyelocytic leukemia 9.7
1052 gastric cancer 9.7
1053 pulmonary hypertension 9.7
1054 acute lymphoblastic leukemia, childhood 9.7
1055 chronic kidney failure 9.7
1056 epidermolysis bullosa dystrophica 9.7
1057 nephrolithiasis 9.7
1058 small cell carcinoma 9.7
1059 cervical dystonia 9.7
1060 autism spectrum disorder 9.7
1061 fibrous dysplasia 9.7
1062 meningococcal meningitis 9.7
1063 amyotrophic neuralgia 9.7
1064 hemiplegia 9.7
1065 placenta praevia 9.7
1066 lyme disease 9.7
1067 clubfoot 9.7
1068 nephrotic syndrome 9.7
1069 hemosiderosis 9.7
1070 gout 9.7
1071 congenital toxoplasmosis 9.7
1072 cholestasis 9.7
1073 prostatitis 9.7
1074 echinococcosis 9.7
1075 disease of mental health 9.7
1076 conversion disorder 9.7
1077 hepatitis c 9.7
1078 basal cell carcinoma 9.7
1079 mesenchymoma 9.7
1080 transitional cell carcinoma 9.7
1081 leydig cell tumor 9.7
1082 acute pancreatitis 9.7
1083 bone inflammation disease 9.7
1084 sertoli cell tumor 9.7
1085 epidural neoplasm 9.7
1086 myopathy 9.7
1087 pleomorphic xanthoastrocytoma 9.7
1088 spindle cell hemangioma 9.7
1089 chronic inflammatory demyelinating polyradiculoneuropathy 9.7
1090 mature teratoma 9.7
1091 aortic valve insufficiency 9.7
1092 malignant mesenchymoma 9.7
1093 progressive multifocal leukoencephalopathy 9.7
1094 hyperthyroidism 9.7
1095 perinatal necrotizing enterocolitis 9.7
1096 epididymo-orchitis 9.7
1097 intracranial hypertension 9.7
1098 fasciitis 9.7
1099 rere-related disorders 9.7
1100 amniotic band syndrome 9.7
1101 cluster headache 9.7
1102 congenital rubella 9.7
1103 germ cells tumors 9.7
1104 homologous wasting disease 9.7
1105 mycobacterium abscessus 9.7
1106 weber syndrome 9.7
1107 angioosteohypertrophic syndrome 9.7
1108 radiation myelitis 9.7
1109 leukemia, chronic lymphocytic 2 9.6
1110 radin blood group antigen 9.6
1111 blood group--wright antigen 9.6
1112 leukocyte adhesion deficiency, type i 9.6
1113 attention deficit-hyperactivity disorder 9.6
1114 laryngomalacia 9.6
1115 leukemia, chronic lymphocytic 9.6
1116 myositis 9.6
1117 paget disease of bone 3 9.6
1118 pheochromocytoma 9.6
1119 polykaryocytosis inducer 9.6
1120 mccune-albright syndrome 9.6
1121 anus, imperforate 9.6
1122 neuropathy, hereditary sensory and autonomic, type iii 9.6
1123 jejunal atresia 9.6
1124 thymoma, familial 9.6
1125 graves disease 1 9.6
1126 immunodysregulation, polyendocrinopathy, and enteropathy, x-linked 9.6
1127 dystonia 9 9.6
1128 suppression of tumorigenicity 12 9.6
1129 lymphoma, non-hodgkin, familial 9.6
1130 coronary heart disease 1 9.6
1131 ovarian cancer 1 9.6
1132 endometrial cancer 9.6
1133 major depressive disorder 9.6
1134 deafness-infertility syndrome 9.6
1135 bone mineral density quantitative trait locus 8 9.6
1136 ewing sarcoma 9.6
1137 bone mineral density quantitative trait locus 15 9.6
1138 meconium ileus 9.6
1139 twin-to-twin transfusion syndrome 9.6
1140 bone fracture 9.6
1141 diabetic foot ulcers 9.6
1142 diamond-blackfan anemia 9.6
1143 ischemic heart disease 9.6
1144 liver disease 9.6
1145 lymphoblastic lymphoma 9.6
1146 marginal zone b-cell lymphoma 9.6
1147 pol iii-related leukodystrophies 9.6
1148 polycystic ovary syndrome 9.6
1149 sacrococcygeal teratoma 9.6
1150 metabolic acidosis 9.6
1151 sleep apnea 9.6
1152 clostridium difficile colitis 9.6
1153 stuttering 9.6
1154 siderosis 9.6
1155 spondyloarthropathy 9.6
1156 megacolon 9.6
1157 pyelonephritis 9.6
1158 mitral valve insufficiency 9.6
1159 optic neuritis 9.6
1160 pulmonary alveolar proteinosis 9.6
1161 patulous eustachian tube 9.6
1162 bronchus cancer 9.6
1163 patent foramen ovale 9.6
1164 amenorrhea 9.6
1165 cholera 9.6
1166 thrombocytopenia due to platelet alloimmunization 9.6
1167 neuroendocrine tumor 9.6
1168 viral hepatitis 9.6
1169 gaucher's disease 9.6
1170 cholecystitis 9.6
1171 post-traumatic stress disorder 9.6
1172 ankylosis 9.6
1173 cystadenoma 9.6
1174 endometriosis 9.6
1175 pulmonary tuberculosis 9.6
1176 antiphospholipid syndrome 9.6
1177 gliosarcoma 9.6
1178 thymoma 9.6
1179 purpura 9.6
1180 neurofibrosarcoma 9.6
1181 choriocarcinoma 9.6
1182 extramedullary plasmacytoma 9.6
1183 pleural empyema 9.6
1184 placental insufficiency 9.6
1185 erdheim-chester disease 9.6
1186 neuromuscular disease 9.6
1187 ganglioneuroma 9.6
1188 myoblastoma 9.6
1189 endometrial stromal tumor 9.6
1190 central nervous system vasculitis 9.6
1191 tanycytic ependymoma 9.6
1192 clear cell ependymoma 9.6
1193 acute t cell leukemia 9.6
1194 lymphopenia 9.6
1195 sarcomatosis 9.6
1196 lung disease 9.6
1197 evans' syndrome 9.6
1198 toxocariasis 9.6
1199 hypereosinophilic syndrome 9.6
1200 hypoglycemia 9.6
1201 acute monoblastic leukemia 9.6
1202 anaplastic ganglioglioma 9.6
1203 anaplastic oligodendroglioma 9.6
1204 bowenoid papulosis 9.6
1205 fetal methylmercury syndrome 9.6
1206 heparin-induced thrombocytopenia 9.6
1207 leukemia, b-cell, chronic 9.6
1208 limbic encephalitis 9.6
1209 lipogranulomatosis 9.6
1210 lymphosarcoma 9.6
1211 plasmablastic lymphoma 9.6
1212 seizure disorder 9.6
1213 superficial siderosis 9.6
1214 myelocystocele 9.6
1215 isolated optic neuritis 9.6
1216 osteoporotic fracture 9.6
1217 pfeiffer syndrome 9.6
1218 arteries, anomalies of 9.6
1219 blue rubber bleb nevus 9.6
1220 cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1 9.6
1221 exudative vitreoretinopathy 1 9.6
1222 hairy nose tip 9.6
1223 diaphragmatic hernia, congenital 9.6
1224 meckel diverticulum 9.6
1225 medulloblastoma 9.6
1226 nephrolithiasis, calcium oxalate 9.6
1227 pityriasis rubra pilaris 9.6
1228 protoporphyria, erythropoietic, 1 9.6
1229 pulmonary hypertension, primary, 1 9.6
1230 scleroderma, familial progressive 9.6
1231 digeorge syndrome 9.6
1232 thyroid cancer, nonmedullary, 1 9.6
1233 tracheoesophageal fistula with or without esophageal atresia 9.6
1234 trigeminal neuralgia 9.6
1235 williams-beuren syndrome 9.6
1236 alexander disease 9.6
1237 chediak-higashi syndrome 9.6
1238 chordoma 9.6
1239 galactorrhea 9.6
1240 biotinidase deficiency 9.6
1241 neutrophil actin dysfunction 9.6
1242 ocular motor apraxia 9.6
1243 respiratory distress syndrome in premature infants 9.6
1244 oncocytoma 9.6
1245 neuronopathy, distal hereditary motor, type viii 9.6
1246 xanthomatosis 9.6
1247 brittle bone disorder 9.6
1248 aneurysmal bone cysts 9.6
1249 scheie syndrome 9.6
1250 autoimmune disease 1 9.6
1251 alpha/beta t-cell lymphopenia with gamma/delta t-cell expansion, severe cytomegalovirus infection, and autoimmunity 9.6
1252 intraocular pressure quantitative trait locus 9.6
1253 encephalocraniocutaneous lipomatosis 9.6
1254 muscle hypertrophy 9.6
1255 hemorrhage, intracerebral 9.6
1256 cholangiocarcinoma 9.6
1257 chronic ulcer of skin 9.6
1258 alcohol abuse 9.6
1259 anaplastic large cell lymphoma 9.6
1260 brain ischemia 9.6
1261 lymphomatoid granulomatosis 9.6
1262 megakaryocytic leukemia 9.6
1263 newborn respiratory distress syndrome 9.6
1264 systemic scleroderma 9.6
1265 ulcerative colitis 9.6
1266 secondary progressive multiple sclerosis 9.6
1267 infective endocarditis 9.6
1268 latex allergy 9.6
1269 recessive dystrophic epidermolysis bullosa 9.6
1270 miyoshi muscular dystrophy 9.6
1271 intrahepatic cholestasis of pregnancy 9.6
1272 obstructive nephropathy 9.6
1273 childhood acute myeloid leukemia 9.6
1274 bone resorption disease 9.6
1275 asymptomatic neurosyphilis 9.6
1276 endocarditis 9.6
1277 esophageal atresia 9.6
1278 meningoencephalitis 9.6
1279 glucose intolerance 9.6
1280 hypoparathyroidism 9.6
1281 esophageal varix 9.6
1282 t cell deficiency 9.6
1283 neonatal anemia 9.6
1284 disseminated intravascular coagulation 9.6
1285 diphtheria 9.6
1286 autonomic nervous system disease 9.6
1287 chronic laryngitis 9.6
1288 blastomycosis 9.6
1289 telangiectasis 9.6
1290 choreatic disease 9.6
1291 coccidioidomycosis 9.6
1292 hyperparathyroidism 9.6
1293 beriberi 9.6
1294 squamous cell papilloma 9.6
1295 plasmodium falciparum malaria 9.6
1296 frozen shoulder 9.6
1297 vacterl association 9.6
1298 keratosis 9.6
1299 histoplasmosis 9.6
1300 status epilepticus 9.6
1301 epilepsy 9.6
1302 hypogonadism 9.6
1303 dysostosis 9.6
1304 adenosarcoma 9.6
1305 enthesopathy 9.6
1306 granular cell tumor 9.6
1307 granulomatous angiitis 9.6
1308 morphine dependence 9.6
1309 cystic teratoma 9.6
1310 synovitis 9.6
1311 dyskeratosis congenita 9.6
1312 bronchiolitis 9.6
1313 bursitis 9.6
1314 lipid metabolism disorder 9.6
1315 progressive muscular atrophy 9.6
1316 central nervous system lymphoma 9.6
1317 vaccinia 9.6
1318 superior mesenteric artery syndrome 9.6
1319 plexopathy 9.6
1320 blood group incompatibility 9.6
1321 carcinosarcoma 9.6
1322 encephalitozoonosis 9.6
1323 granulomatous dermatitis 9.6
1324 rhinitis 9.6
1325 pleomorphic adenoma 9.6
1326 placenta accreta 9.6
1327 pituitary carcinoma 9.6
1328 ureteral obstruction 9.6
1329 demyelinating polyneuropathy 9.6
1330 hemoglobin e disease 9.6
1331 malignant peripheral nerve sheath tumor 9.6
1332 gliomatosis cerebri 9.6
1333 fibromyalgia 9.6
1334 cervical adenoma malignum 9.6
1335 myositis ossificans 9.6
1336 juvenile rheumatoid arthritis 9.6
1337 compartment syndrome 9.6
1338 subacute thyroiditis 9.6
1339 hypogonadotropism 9.6
1340 malignant pleural mesothelioma 9.6
1341 situs inversus 9.6
1342 placenta disease 9.6
1343 intestinal obstruction 9.6
1344 polyhydramnios 9.6
1345 subacute delirium 9.6
1346 erythromelalgia 9.6
1347 necrotizing fasciitis 9.6
1348 systolic heart failure 9.6
1349 yellow fever 9.6
1350 irritable bowel syndrome 9.6
1351 congenital syphilis 9.6
1352 eosinophilia-myalgia syndrome 9.6
1353 morquio syndrome 9.6
1354 col1a1/2-related osteogenesis imperfecta 9.6
1355 afibrinogenemia 9.6
1356 anaplastic oligoastrocytoma 9.6
1357 blastic plasmacytoid dendritic cell 9.6
1358 cerebrospinal fluid leak 9.6
1359 charcot-marie-tooth disease type 2c 9.6
1360 eosinophilic granulomatosis with polyangiitis 9.6
1361 fibrosing mediastinitis 9.6
1362 hip subluxation 9.6
1363 htlv-1 associated myelopathy/tropical spastic paraparesis 9.6
1364 microscopic polyangiitis 9.6
1365 neurogenic hypertension 9.6
1366 oligoastrocytoma 9.6
1367 pyogenic granuloma 9.6
1368 respiratory distress syndrome, infant 9.6
1369 soft tissue sarcoma 9.6
1370 spondyloenchondrodysplasia 9.6
1371 hereditary hypophosphatemic rickets 9.6
1372 rapidly involuting congenital hemangioma 9.6
1373 extraventricular neurocytoma 9.6
1374 serotonin syndrome 9.6
1375 hajdu-cheney syndrome 9.5
1376 alcohol dependence 9.5
1377 angelman syndrome 9.5
1378 apnea, obstructive sleep 9.5
1379 atrial standstill 1 9.5
1380 aortic valve disease 1 9.5
1381 carpal tunnel syndrome 9.5
1382 cleft palate, isolated 9.5
1383 coloboma of macula 9.5
1384 erythermalgia, primary 9.5
1385 floating-harbor syndrome 9.5
1386 hypertriglyceridemia, familial 9.5
1387 kaposi sarcoma 9.5
1388 keratitis, hereditary 9.5
1389 leukemia, acute monocytic 9.5
1390 melorheostosis, isolated 9.5
1391 antigen defined by monoclonal antibody aj9 9.5
1392 myoclonus and ataxia 9.5
1393 carney complex, type 1 9.5
1394 pelvic organ prolapse 9.5
1395 proteus syndrome 9.5
1396 raynaud disease 9.5
1397 scapuloperoneal spinal muscular atrophy 9.5
1398 tetralogy of fallot 9.5
1399 triiodothyronine receptor auxiliary protein 9.5
1400 vater/vacterl association 9.5
1401 takayasu arteritis 9.5
1402 diastrophic dysplasia 9.5
1403 hypoplastic left heart syndrome 1 9.5
1404 mucolipidosis ii alpha/beta 9.5
1405 niemann-pick disease, type a 9.5
1406 pancreatic cancer 9.5
1407 polyglucosan body neuropathy, adult form 9.5
1408 pyruvate kinase deficiency of red cells 9.5
1409 xeroderma pigmentosum, variant type 9.5
1410 androgen insensitivity syndrome 9.5
1411 lesch-nyhan syndrome 9.5
1412 severe combined immunodeficiency, x-linked 9.5
1413 hypophosphatemic rickets, x-linked recessive 9.5
1414 bornholm eye disease 9.5
1415 pigmentary disorder, reticulate, with systemic manifestations, x-linked 9.5
1416 colonic atresia 9.5
1417 opitz-kaveggia syndrome 9.5
1418 exstrophy of bladder 9.5
1419 helicobacter pylori infection 9.5
1420 frontotemporal dementia 9.5
1421 adenomyosis 9.5
1422 pleuropulmonary blastoma 9.5
1423 chondrodysplasia punctata, brachytelephalangic, autosomal 9.5
1424 caronte 9.5
1425 aceruloplasminemia 9.5
1426 ascaris lumbricoides infection 9.5
1427 salla disease 9.5
1428 nasopharyngeal carcinoma 9.5
1429 allergic rhinitis 9.5
1430 headache associated with sexual activity 9.5
1431 tropical calcific pancreatitis 9.5
1432 granulomatosis with polyangiitis 9.5
1433 spondylocostal dysostosis 3, autosomal recessive 9.5
1434 chromosome 16p13.3 deletion syndrome, proximal 9.5
1435 diabetes mellitus, ketosis-prone 9.5
1436 pseudopseudohypoparathyroidism 9.5
1437 microvascular complications of diabetes 3 9.5
1438 microvascular complications of diabetes 4 9.5
1439 microvascular complications of diabetes 6 9.5
1440 microvascular complications of diabetes 7 9.5
1441 mononeuropathy of the median nerve, mild 9.5
1442 human herpesvirus 8 9.5
1443 leptin deficiency or dysfunction 9.5
1444 global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies 9.5
1445 alport syndrome 9.5
1446 b-cell lymphomas 9.5
1447 cerebral hemorrhage 9.5
1448 common variable immunodeficiency 9.5
1449 coronary artery anomaly 9.5
1450 end stage renal failure 9.5
1451 hereditary hemorrhagic telangiectasia 9.5
1452 holoprosencephaly 9.5
1453 human venous malformation 9.5
1454 hypoplastic left heart syndrome 9.5
1455 insulinoma 9.5
1456 malignant glioma 9.5
1457 muscle disorders 9.5
1458 niemann-pick disease 9.5
1459 peripheral t-cell lymphoma 9.5
1460 pulmonary fibrosis 9.5
1461 sinusitis 9.5
1462 testicular lymphoma 9.5
1463 invasive aspergillosis 9.5
1464 aspiration pneumonia 9.5
1465 paralytic poliomyelitis 9.5
1466 hereditary sensory neuropathy 9.5
1467 t-cell large granular lymphocyte leukemia 9.5
1468 renal fibrosis 9.5
1469 inflammatory myofibroblastic tumor 9.5
1470 brain glioma 9.5
1471 alexithymia 9.5
1472 umbilical hernia 9.5
1473 zika fever 9.5
1474 cryptococcal meningitis 9.5
1475 nonalcoholic fatty liver disease 9.5
1476 dry eye syndrome 9.5
1477 spindle cell lipoma 9.5
1478 dermatomyositis 9.5
1479 mumps 9.5
1480 pneumoconiosis 9.5
1481 chronic leukemia 9.5
1482 bacterial infectious disease 9.5
1483 hypopyon 9.5
1484 osteomalacia 9.5
1485 thrombotic thrombocytopenic purpura 9.5
1486 amnestic disorder 9.5
1487 spastic quadriplegia 9.5
1488 brucellosis 9.5
1489 hemopericardium 9.5
1490 cardiac tamponade 9.5
1491 iron deficiency anemia 9.5
1492 gastroparesis 9.5
1493 hematocele of tunica vaginalis testis 9.5
1494 pancytopenia 9.5
1495 secondary hyperparathyroidism 9.5
1496 paracoccidioidomycosis 9.5
1497 hereditary spherocytosis 9.5
1498 hellp syndrome 9.5
1499 typhoid fever 9.5
1500 pure red-cell aplasia 9.5
1501 interstitial cystitis 9.5
1502 toxic shock syndrome 9.5
1503 azoospermia 9.5
1504 glossitis 9.5
1505 laryngeal tuberculosis 9.5
1506 lymphadenitis 9.5
1507 pneumothorax 9.5
1508 urethral stricture 9.5
1509 hyperinsulinism 9.5
1510 nocardiosis 9.5
1511 colon adenocarcinoma 9.5
1512 acromegaly 9.5
1513 juxtacortical chondroma 9.5
1514 lymphangiosarcoma 9.5
1515 contact dermatitis 9.5
1516 acalculous cholecystitis 9.5
1517 severe acute respiratory syndrome 9.5
1518 cystic kidney disease 9.5
1519 sertoli-leydig cell tumor 9.5
1520 churg-strauss syndrome 9.5
1521 ascaridiasis 9.5
1522 causalgia 9.5
1523 embryonal rhabdomyosarcoma 9.5
1524 angiomyolipoma 9.5
1525 turner syndrome 9.5
1526 lactic acidosis 9.5
1527 rhabdoid cancer 9.5
1528 olfactory neuroblastoma 9.5
1529 gastritis 9.5
1530 melorheostosis 9.5
1531 bone giant cell tumor 9.5
1532 embryoma 9.5
1533 ependymoblastoma 9.5
1534 intrahepatic cholangiocarcinoma 9.5
1535 retroperitoneal leiomyosarcoma 9.5
1536 testicular yolk sac tumor 9.5
1537 papillary ependymoma 9.5
1538 malignant teratoma 9.5
1539 meningeal melanocytoma 9.5
1540 reactive arthritis 9.5
1541 cowden syndrome 9.5
1542 prion disease 9.5
1543 kummell's disease 9.5
1544 lumbosacral lipoma 9.5
1545 astroblastoma 9.5
1546 parathyroid adenoma 9.5
1547 testicular fibroma 9.5
1548 mediastinitis 9.5
1549 peritonitis 9.5
1550 scabies 9.5
1551 intestinal volvulus 9.5
1552 pellagra 9.5
1553 whipple disease 9.5
1554 monocytic leukemia 9.5
1555 hodgkin's lymphoma, lymphocytic-histiocytic predominance 9.5
1556 malignant histiocytosis 9.5
1557 eating disorder 9.5
1558 leishmaniasis 9.5
1559 hypertensive encephalopathy 9.5
1560 fatty liver disease 9.5
1561 bronchiectasis 9.5
1562 placental abruption 9.5
1563 uterine inversion 9.5
1564 hyperphenylalaninemia 9.5
1565 polycystic kidney disease 9.5
1566 adult polyglucosan body disease 9.5
1567 acroosteolysis dominant type 9.5
1568 allergic angiitis 9.5
1569 aplasia cutis congenita 9.5
1570 athetosis 9.5
1571 candida glabrata 9.5
1572 congenital torticollis 9.5
1573 congenital zika syndrome 9.5
1574 degos 'en cocarde' erythrokeratoderma 9.5
1575 dendritic cell tumor 9.5
1576 dextrocardia with situs inversus 9.5
1577 diffuse neonatal hemangiomatosis 9.5
1578 frontal fibrosing alopecia 9.5
1579 haemophilus influenzae 9.5
1580 human t-cell leukemia virus type 1 9.5
1581 large granular lymphocyte leukemia 9.5
1582 lymphangiectasis 9.5
1583 mediastinal endodermal sinus tumors 9.5
1584 mycobacterium marinum 9.5
1585 pudendal neuralgia 9.5
1586 retroperitoneal fibrosis 9.5
1587 retroperitoneal liposarcoma 9.5
1588 secondary adrenal insufficiency 9.5
1589 spondylarthropathy 9.5
1590 syringobulbia 9.5
1591 thrombasthenia 9.5
1592 tracheoesophageal fistula 9.5
1593 xp22.3 microdeletion syndrome 9.5
1594 zika virus infection 9.5
1595 myotonia 9.5
1596 foot drop 9.5
1597 mixed germ cell tumor 9.5
1598 neurotrophic keratopathy 9.5
1599 epithelioid hemangioendothelioma 9.5
1600 infantile krabbe disease 9.5
1601 argyria 9.5
1602 pneumococcal meningitis 9.5
1603 myxofibrosarcoma 9.5
1604 diffuse alveolar hemorrhage 9.5
1605 histiocytic sarcoma 9.5
1606 acute adrenal insufficiency 9.5
1607 acroosteolysis 9.3
1608 cerebral amyloid angiopathy, cst3-related 9.3
1609 anisocoria 9.3
1610 atherosclerosis susceptibility 9.3
1611 biliary cirrhosis, primary, 1 9.3
1612 blood group system, landsteiner-wiener 9.3
1613 progressive familial heart block, type ia 9.3
1614 cardiac arrhythmia 9.3
1615 cardiac conduction defect 9.3
1616 hypercarotenemia and vitamin a deficiency, autosomal dominant 9.3
1617 klippel-feil syndrome 1, autosomal dominant 9.3
1618 charcot-marie-tooth disease, demyelinating, type 1a 9.3
1619 coarctation of aorta 9.3
1620 dentatorubral-pallidoluysian atrophy 9.3
1621 diabetes insipidus, nephrogenic, autosomal 9.3
1622 pilomatrixoma 9.3
1623 esterase c 9.3
1624 fibrodysplasia ossificans progressiva 9.3
1625 fish-eye disease 9.3
1626 hernia, hiatus 9.3
1627 hypercholesterolemia, familial 9.3
1628 endosteal hyperostosis, autosomal dominant 9.3
1629 pallister-hall syndrome 9.3
1630 intussusception 9.3
1631 trichorhinophalangeal syndrome, type ii 9.3
1632 larsen syndrome 9.3
1633 lichen sclerosus et atrophicus 9.3
1634 progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 1 9.3
1635 moebius syndrome 9.3
1636 motion sickness 9.3
1637 cowden syndrome 1 9.3
1638 dystonia 11, myoclonic 9.3
1639 amyotrophy, hereditary neuralgic 9.3
1640 neutrophil migration 9.3
1641 noonan syndrome 1 9.3
1642 obsessive-compulsive disorder 9.3
1643 osteogenesis imperfecta, type ii 9.3
1644 otitis media 9.3
1645 leukodystrophy, demyelinating, adult-onset, autosomal dominant 9.3
1646 pilonidal sinus 9.3
1647 prader-willi syndrome 9.3
1648 premature chromatid separation trait 9.3
1649 pulmonary fibrosis, idiopathic 9.3
1650 silver-russell syndrome 9.3
1651 ruvalcaba syndrome 9.3
1652 spondyloepiphyseal dysplasia congenita 9.3
1653 thanatophoric dysplasia, type i 9.3
1654 thrombophilia due to activated protein c resistance 9.3
1655 suppressor of tumorigenicity 3 9.3
1656 vertigo, benign recurrent 9.3
1657 whim syndrome 9.3
1658 wolf-hirschhorn syndrome 9.3
1659 wolff-parkinson-white syndrome 9.3
1660 abetalipoproteinemia 9.3
1661 lipoid congenital adrenal hyperplasia 9.3
1662 adrenocortical carcinoma, hereditary 9.3
1663 alkaptonuria 9.3
1664 tangier disease 9.3
1665 ataxia-telangiectasia 9.3
1666 australia antigen 9.3
1667 central hypoventilation syndrome, congenital 9.3
1668 sitosterolemia 9.3
1669 charge syndrome 9.3
1670 costello syndrome 9.3
1671 cystic fibrosis 9.3
1672 cystinuria 9.3
1673 leukoencephalopathy, hereditary diffuse, with spheroids 9.3
1674 disorganization, mouse, homolog of 9.3
1675 ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive 9.3
1676 factor vii deficiency 9.3
1677 farber lipogranulomatosis 9.3
1678 myofibromatosis, infantile, 1 9.3
1679 fibrosclerosis, multifocal 9.3
1680 glaucoma 3, primary congenital, a 9.3
1681 hemochromatosis, type 1 9.3
1682 hypoascorbemia 9.3
1683 immunoerythromyeloid hypoplasia 9.3
1684 indifference to pain, congenital, autosomal recessive 9.3
1685 keratoconus posticus circumscriptus 9.3
1686 donohue syndrome 9.3
1687 maple syrup urine disease 9.3
1688 nijmegen breakage syndrome 9.3
1689 moyamoya disease 1 9.3
1690 mucopolysaccharidosis, type iiib 9.3
1691 mucopolysaccharidosis, type iva 9.3
1692 mucopolysaccharidosis, type vi 9.3
1693 mucopolysaccharidosis, type vii 9.3
1694 myxedema 9.3
1695 osteoid osteoma 9.3
1696 chronic recurrent multifocal osteomyelitis 9.3
1697 osteopetrosis, autosomal recessive 2 9.3
1698 shwachman-diamond syndrome 1 9.3
1699 pulmonary alveolar microlithiasis 9.3
1700 pulmonary venoocclusive disease 1, autosomal dominant 9.3
1701 reticular dysgenesis 9.3
1702 reticulum cell sarcoma 9.3
1703 rhabdomyosarcoma 2 9.3
1704 rothmund-thomson syndrome 9.3
1705 spastic paraplegia 17, autosomal dominant 9.3
1706 multiple sulfatase deficiency 9.3
1707 glanzmann thrombasthenia 9.3
1708 mismatch repair cancer syndrome 9.3
1709 werner syndrome 9.3
1710 lysosomal acid lipase deficiency 9.3
1711 muscular dystrophy, becker type 9.3
1712 bone mineral density quantitative trait locus 18 9.3
1713 chondrodysplasia punctata 1, x-linked recessive 9.3
1714 granulomatous disease, chronic, x-linked 9.3
1715 hemophilia b 9.3
1716 congenital hemidysplasia with ichthyosiform erythroderma and limb defects 9.3
1717 lymphoproliferative syndrome, x-linked, 1 9.3
1718 mucopolysaccharidosis, type ii 9.3
1719 thoracoabdominal syndrome 9.3
1720 cyclic vomiting syndrome 9.3
1721 pituitary adenoma, prolactin-secreting 9.3
1722 renal dysplasia, cystic 9.3
1723 pallister-killian syndrome 9.3
1724 alzheimer disease 5 9.3
1725 malignant atrophic papulosis 9.3
1726 astigmatism 9.3
1727 homocysteinemia 9.3
1728 polydactyly 9.3
1729 ovarian germ cell cancer 9.3
1730 urinary tract infections, recurrent 9.3
1731 spastic paraplegia 10, autosomal dominant 9.3
1732 amegakaryocytic thrombocytopenia, congenital 9.3
1733 progressive familial heart block, type ib 9.3
1734 orthostatic intolerance 9.3
1735 hydronephrosis, congenital, with cleft palate, characteristic facies, hypotonia, and mental retardation 9.3
1736 glycine encephalopathy 9.3
1737 alveolar soft part sarcoma 9.3
1738 alzheimer disease 4 9.3
1739 bone mineral density quantitative trait locus 3 9.3
1740 pulmonary disease, chronic obstructive 9.3
1741 lissencephaly 1 9.3
1742 psoriatic arthritis 9.3
1743 irak4 deficiency 9.3
1744 mycobacterium tuberculosis 1 9.3
1745 severe cutaneous adverse reaction 9.3
1746 avascular necrosis of femoral head, primary, 1 9.3
1747 progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 2 9.3
1748 progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 3 9.3
1749 mental retardation, enteropathy, deafness, peripheral neuropathy, ichthyosis, and keratoderma 9.3
1750 hepatitis c virus 9.3
1751 noonan syndrome 3 9.3
1752 progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 4 9.3
1753 mevalonic aciduria 9.3
1754 microvascular complications of diabetes 5 9.3
1755 porphyria, acute hepatic 9.3
1756 synesthesia 9.3
1757 purine nucleoside phosphorylase deficiency 9.3
1758 muscular dystrophy, congenital, lmna-related 9.3
1759 tuberous sclerosis 2 9.3
1760 alpha-1-antitrypsin deficiency 9.3
1761 fetal hemoglobin quantitative trait locus 6 9.3
1762 complement component 3 deficiency, autosomal recessive 9.3
1763 protein z deficiency 9.3
1764 encephalopathy, acute, infection-induced 4 9.3
1765 vesicoureteral reflux 6 9.3
1766 blood group, junior system 9.3
1767 charcot-marie-tooth disease, axonal, type 2r 9.3
1768 hyperprolactinemia 9.3
1769 melioidosis 9.3
1770 blood group, gerbich system 9.3
1771 autoimmune lymphoproliferative syndrome, type v 9.3
1772 nevus comedonicus 9.3
1773 lymphatic malformation 7 9.3
1774 helix syndrome 9.3
1775 baker-gordon syndrome 9.3
1776 mucocutaneous ulceration, chronic 9.3
1777 tendinopathy 9.3
1778 tendinitis 9.3
1779 adrenal cortical carcinoma 9.3
1780 adult respiratory distress syndrome 9.3
1781 brain glioblastoma multiforme 9.3
1782 bronchiolitis obliterans 9.3
1783 burn scar 9.3
1784 childhood type dermatomyositis 9.3
1785 chronic angina 9.3
1786 chronic myelomonocytic leukemia 9.3
1787 chronic myocardial ischemia 9.3
1788 congenital hypomyelination neuropathy 9.3
1789 craniosynostosis 9.3
1790 degenerative disc disease 9.3
1791 ectodermal dysplasia 9.3
1792 follicular lymphoma 9.3
1793 gas gangrene 9.3
1794 gingival recession 9.3
1795 glycogen storage disease 9.3
1796 hematologic cancer 9.3
1797 ischemic optic neuropathy 9.3
1798 islet cell tumor 9.3
1799 keratopathy 9.3
1800 lymphedema 9.3
1801 lymphoid leukemia 9.3
1802 lysosomal storage disease 9.3
1803 mannosidosis 9.3
1804 mantle cell lymphoma 9.3
1805 melanoma metastasis 9.3
1806 osteonecrosis 9.3
1807 pancreas adenocarcinoma 9.3
1808 pancreatic ductal adenocarcinoma 9.3
1809 pemphigus foliaceus 9.3
1810 primary biliary cirrhosis 9.3
1811 pseudoarthrosis 9.3
1812 waldenstrom macroglobulinemia 9.3
1813 angiosarcoma 9.3
1814 dengue shock syndrome 9.3
1815 tick-borne encephalitis 9.3
1816 fusariosis 9.3
1817 trichosporonosis 9.3
1818 hypophosphatemia 9.3
1819 hyperphosphatemia 9.3
1820 loeys-dietz syndrome 9.3
1821 exanthem 9.3
1822 multinodular goiter 9.3
1823 asphyxiating thoracic dystrophy 9.3
1824 intestinal schistosomiasis 9.3
1825 distal arthrogryposis 9.3
1826 fetal alcohol syndrome 9.3
1827 alcohol-related birth defect 9.3
1828 spastic cerebral palsy 9.3
1829 serine deficiency 9.3
1830 rheumatic heart disease 9.3
1831 peripheral artery disease 9.3
1832 colorectal adenocarcinoma 9.3
1833 adrenal gland pheochromocytoma 9.3
1834 ameloblastoma 9.3
1835 ovarian serous carcinoma 9.3
1836 cd40 ligand deficiency 9.3
1837 osteoblastoma 9.3
1838 cerebellar medulloblastoma 9.3
1839 apraxia 9.3
1840 diversion colitis 9.3
1841 crohn's colitis 9.3
1842 balo concentric sclerosis 9.3
1843 crest syndrome 9.3
1844 gallbladder disease 9.3
1845 pollen allergy 9.3
1846 spinal disease 9.3
1847 atypical chronic myeloid leukemia 9.3
1848 hypomyelinating leukodystrophy 9.3
1849 physical disorder 9.3
1850 infantile myofibromatosis 9.3
1851 esophageal atresia/tracheoesophageal fistula 9.3
1852 hepatic veno-occlusive disease 9.3
1853 mucositis 9.3
1854 renal hypoplasia 9.3
1855 chronic eosinophilic leukemia 9.3
1856 mucolipidosis 9.3
1857 hypogonadotropic hypogonadism 9.3
1858 angioimmunoblastic t-cell lymphoma 9.3
1859 multicentric castleman disease 9.3
1860 castleman disease 9.3
1861 thyroid lymphoma 9.3
1862 endometritis 9.3
1863 corneal disease 9.3
1864 thymus lymphoma 9.3
1865 cholelithiasis 9.3
1866 ehrlichiosis 9.3
1867 pleurisy 9.3
1868 louping ill 9.3
1869 anthracosis 9.3
1870 chronic meningitis 9.3
1871 natural killer cell leukemia 9.3
1872 prolymphocytic leukemia 9.3
1873 common cold 9.3
1874 interstitial nephritis 9.3
1875 cystinosis 9.3
1876 chronic pyelonephritis 9.3
1877 portal hypertension 9.3
1878 mesenteric lymphadenitis 9.3
1879 filariasis 9.3
1880 gastric ulcer 9.3
1881 dirofilariasis 9.3
1882 malignant hypertension 9.3
1883 abducens nerve disease 9.3
1884 hypospadias 9.3
1885 spastic diplegia 9.3
1886 spastic hemiplegia 9.3
1887 discitis 9.3
1888 meconium aspiration syndrome 9.3
1889 myiasis 9.3
1890 henoch-schoenlein purpura 9.3
1891 anhidrosis 9.3
1892 primary hyperparathyroidism 9.3
1893 anemia of prematurity 9.3
1894 vitamin k deficiency bleeding 9.3
1895 ornithosis 9.3
1896 keratomalacia 9.3
1897 schizophreniform disorder 9.3
1898 gnathomiasis 9.3
1899 xanthogranulomatous pyelonephritis 9.3
1900 hypertensive heart disease 9.3
1901 streptococcal meningitis 9.3
1902 pericardial effusion 9.3
1903 cortical blindness 9.3
1904 esophagitis 9.3
1905 spermatocele 9.3
1906 conn's syndrome 9.3
1907 cryptococcosis 9.3
1908 low compliance bladder 9.3
1909 alveolar echinococcosis 9.3
1910 lymphocytic choriomeningitis 9.3
1911 vogt-koyanagi-harada disease 9.3
1912 graves' disease 9.3
1913 von willebrand's disease 9.3
1914 hepatitis a 9.3
1915 hepatic coma 9.3
1916 chronic progressive external ophthalmoplegia 9.3
1917 pyloric stenosis 9.3
1918 locked-in syndrome 9.3
1919 rectal disease 9.3
1920 relapsing fever 9.3
1921 renal osteodystrophy 9.3
1922 vertebral artery insufficiency 9.3
1923 uveitis 9.3
1924 endemic goiter 9.3
1925 right bundle branch block 9.3
1926 pneumatosis cystoides intestinalis 9.3
1927 mesenteric vascular occlusion 9.3
1928 porphyria 9.3
1929 intestinal tuberculosis 9.3
1930 hepatic encephalopathy 9.3
1931 tuberous sclerosis 9.3
1932 obstructive jaundice 9.3
1933 sapho syndrome 9.3
1934 endometrial stromal nodule 9.3
1935 lymphogranuloma venereum 9.3
1936 facial paralysis 9.3
1937 benign paroxysmal positional nystagmus 9.3
1938 selective igg deficiency disease 9.3
1939 ochronosis 9.3
1940 oral candidiasis 9.3
1941 patellofemoral pain syndrome 9.3
1942 generalized anxiety disorder 9.3
1943 suppurative thyroiditis 9.3
1944 dracunculiasis 9.3
1945 pemphigoid gestationis 9.3
1946 reye syndrome 9.3
1947 cholesterol embolism 9.3
1948 hereditary angioedema 9.3
1949 olivopontocerebellar atrophy 9.3
1950 candidiasis 9.3
1951 panniculitis 9.3
1952 angioedema 9.3
1953 communicating hydrocephalus 9.3
1954 rheumatic disease 9.3
1955 mental depression 9.3
1956 ventricular septal defect 9.3
1957 pineoblastoma 9.3
1958 richter's syndrome 9.3
1959 factitious disorder 9.3
1960 toxic megacolon 9.3
1961 pericarditis 9.3
1962 peritoneal mesothelioma 9.3
1963 telogen effluvium 9.3
1964 syringoma 9.3
1965 essential thrombocythemia 9.3
1966 pharyngitis 9.3
1967 dyspepsia 9.3
1968 glomus tumor 9.3
1969 thrombophilia 9.3
1970 gastric antral vascular ectasia 9.3
1971 relapsing polychondritis 9.3
1972 rhizomelic chondrodysplasia punctata 9.3
1973 adenomyoma 9.3
1974 kidney cancer 9.3
1975 ossifying fibromyxoid tumor 9.3
1976 chorioangioma 9.3
1977 glucosephosphate dehydrogenase deficiency 9.3
1978 laryngeal squamous cell carcinoma 9.3
1979 iga glomerulonephritis 9.3
1980 germ cell cancer 9.3
1981 substance abuse 9.3
1982 giant cell glioblastoma 9.3
1983 cystic lymphangioma 9.3
1984 idiopathic cd4-positive t-lymphocytopenia 9.3
1985 gallbladder cancer 9.3
1986 keratoacanthoma 9.3
1987 neurilemmomatosis 9.3
1988 tracheal stenosis 9.3
1989 gastric dilatation 9.3
1990 thymic carcinoma 9.3
1991 embryonal carcinoma 9.3
1992 mood disorder 9.3
1993 osteitis fibrosa 9.3
1994 small cell osteogenic sarcoma 9.3
1995 inappropriate adh syndrome 9.3
1996 skin carcinoma 9.3
1997 breast adenocarcinoma 9.3
1998 cellulitis 9.3
1999 congenital myasthenic syndrome 9.3
2000 cervical adenocarcinoma 9.3
2001 theileriasis 9.3
2002 hermaphroditism 9.3
2003 cranial nerve palsy 9.3
2004 thrombophlebitis 9.3
2005 acute myocarditis 9.3
2006 adrenal cortical adenocarcinoma 9.3
2007 merkel cell carcinoma 9.3
2008 bladder urothelial carcinoma 9.3
2009 spindle cell carcinoma 9.3
2010 granulomatous gastritis 9.3
2011 tricuspid valve insufficiency 9.3
2012 biliary dyskinesia 9.3
2013 rh isoimmunization 9.3
2014 mutism 9.3
2015 femoral neuropathy 9.3
2016 hair disease 9.3
2017 pyoderma 9.3
2018 akinetic mutism 9.3
2019 polyradiculopathy 9.3
2020 pustulosis of palm and sole 9.3
2021 juvenile xanthogranuloma 9.3
2022 dysgerminoma 9.3
2023 sarcomatoid mesothelioma 9.3
2024 hypokalemia 9.3
2025 mucoepidermoid carcinoma 9.3
2026 mesenchymal chondrosarcoma 9.3
2027 ulnar neuropathy 9.3
2028 freemartinism 9.3
2029 uremia 9.3
2030 extragonadal germ cell cancer 9.3
2031 medulloepithelioma 9.3
2032 gorham's disease 9.3
2033 myoepithelial carcinoma 9.3
2034 cerebellar astrocytoma 9.3
2035 gliofibroma 9.3
2036 bronchiolo-alveolar adenocarcinoma 9.3
2037 klatskin's tumor 9.3
2038 postpoliomyelitis syndrome 9.3
2039 neurotic disorder 9.3
2040 alcoholic pancreatitis 9.3
2041 atypical polypoid adenomyoma 9.3
2042 subependymal giant cell astrocytoma 9.3
2043 copper deficiency myelopathy 9.3
2044 leiomyomatosis 9.3
2045 plexiform neurofibroma 9.3
2046 arteriosclerosis obliterans 9.3
2047 urinary tract obstruction 9.3
2048 chronic polyneuropathy 9.3
2049 epithelioid leiomyosarcoma 9.3
2050 vulvar leiomyosarcoma 9.3
2051 epithelial-myoepithelial carcinoma 9.3
2052 pulmonary venoocclusive disease 9.3
2053 clear cell adenofibroma 9.3
2054 cystadenofibroma 9.3
2055 pineal region choriocarcinoma 9.3
2056 acute pyelonephritis 9.3
2057 embryonal testis carcinoma 9.3
2058 mixed liposarcoma 9.3
2059 median neuropathy 9.3
2060 diffuse peritoneal leiomyomatosis 9.3
2061 intravenous leiomyomatosis 9.3
2062 adenosine deaminase deficiency 9.3
2063 inferior myocardial infarction 9.3
2064 myxoid chondrosarcoma 9.3
2065 panic disorder 9.3
2066 meningeal melanoma 9.3
2067 mitral valve disease 9.3
2068 cerebellopontine angle meningioma 9.3
2069 viral encephalitis 9.3
2070 overnutrition 9.3
2071 malignant triton tumor 9.3
2072 cerebrovascular disease 9.3
2073 peroneal nerve paralysis 9.3
2074 telangiectatic osteogenic sarcoma 9.3
2075 gemistocytic astrocytoma 9.3
2076 infiltrating lipoma 9.3
2077 leber hereditary optic neuropathy 9.3
2078 melanomatosis 9.3
2079 ovarian serous cystadenofibroma 9.3
2080 pseudosarcomatous fibromatosis 9.3
2081 cerebral primitive neuroectodermal tumor 9.3
2082 pineal region germinoma 9.3
2083 monoclonal gammopathy of uncertain significance 9.3
2084 adenomatoid tumor 9.3
2085 sarcomatosis of the meninges 9.3
2086 macular holes 9.3
2087 carotid artery occlusion 9.3
2088 septic arthritis 9.3
2089 myocarditis 9.3
2090 meningeal melanomatosis 9.3
2091 complement component 3 deficiency 9.3
2092 paralytic ileus 9.3
2093 localized scleroderma 9.3
2094 oropharynx cancer 9.3
2095 vascular dementia 9.3
2096 pyomyositis 9.3
2097 molluscum contagiosum 9.3
2098 chorioretinitis 9.3
2099 psoriasis 9.3
2100 mitochondrial encephalomyopathy 9.3
2101 skin melanoma 9.3
2102 atrophic gastritis 9.3
2103 sideroblastic anemia 9.3
2104 autosomal dominant polycystic kidney disease 9.3
2105 bladder carcinoma in situ 9.3
2106 macroglobulinemia 9.3
2107 rem sleep behavior disorder 9.3
2108 granuloma inguinale 9.3
2109 pemphigus 9.3
2110 homocystinuria 9.3
2111 ocular hypertension 9.3
2112 lymphangitis 9.3
2113 urethral false passage 9.3
2114 hypopituitarism 9.3
2115 postpartum depression 9.3
2116 krukenberg carcinoma 9.3
2117 plantar fasciitis 9.3
2118 hemorrhoid 9.3
2119 trichinosis 9.3
2120 bulbar polio 9.3
2121 neonatal abstinence syndrome 9.3
2122 microcephaly 9.3
2123 acid sphingomyelinase deficiency 9.3
2124 charcot-marie-tooth hereditary neuropathy 9.3
2125 childhood ataxia with central nervous system hypomyelination / vanishing white matter 9.3
2126 juvenile hereditary hemochromatosis 9.3
2127 mitochondrial disorders 9.3
2128 polymicrogyria 9.3
2129 2q37 deletion syndrome 9.3
2130 47, xxy 9.3
2131 acardia 9.3
2132 acute articular rheumatism 9.3
2133 acute leukemia of ambiguous lineage 9.3
2134 acute mountain sickness 9.3
2135 acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22) 9.3
2136 acute necrotizing encephalopathy 9.3
2137 acute posterior multifocal placoid pigment epitheliopathy 9.3
2138 aminoaciduria 9.3
2139 amyloidosis beta2m 9.3
2140 anterior spinal artery stroke 9.3
2141 anterior uveitis 9.3
2142 autoimmune encephalitis 9.3
2143 benign metastasizing leiomyoma 9.3
2144 bone marrow necrosis 9.3
2145 brainstem auditory evoked responses 9.3
2146 broken heart syndrome 9.3
2147 bronchogenic cyst 9.3
2148 carcinoid syndrome 9.3
2149 carcinoma showing thymus-like differentiation 9.3
2150 cerebral palsy athetoid 9.3
2151 childhood non-hodgkin lymphoma 9.3
2152