MCID: NRR001
MIFTS: 42

Neuroretinitis

Categories: Neuronal diseases

Aliases & Classifications for Neuroretinitis

MalaCards integrated aliases for Neuroretinitis:

Name: Neuroretinitis 12 15 71
Juxtapapillary Focal Retinitis and Retinochoroiditis 12 71
Retinitis 43 71
Focal Retinitis and Retinochoroiditis, Juxtapapillary 12
Papilloretinitis 12

Classifications:



External Ids:

Disease Ontology 12 DOID:10176
MeSH 43 D012173
SNOMED-CT 67 410471004
ICD10 32 H30.9
UMLS 71 C0035333 C0154874 C3665438

Summaries for Neuroretinitis

MalaCards based summary : Neuroretinitis, also known as juxtapapillary focal retinitis and retinochoroiditis, is related to central retinal artery occlusion and macular dystrophy, dominant cystoid. An important gene associated with Neuroretinitis is CD40LG (CD40 Ligand), and among its related pathways/superpathways is Visual Cycle in Retinal Rods. The drugs Prednisone and Azithromycin have been mentioned in the context of this disorder. Affiliated tissues include retina, eye and testes.

Wikipedia : 74 Cat-scratch disease (CSD) is an infectious disease that most often results from a scratch or bite of a... more...

Related Diseases for Neuroretinitis

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

(showing 3023, show less)
# Related Disease Score Top Affiliating Genes
1 central retinal artery occlusion 34.1 CRP CD40LG
2 macular dystrophy, dominant cystoid 32.8 RCVRN MRAP ACE
3 fundus dystrophy 31.5 TRPM1 SAG RCVRN MRAP
4 congenital stationary night blindness 31.4 TRPM1 SAG RCVRN
5 acquired night blindness 31.4 TRPM1 RCVRN
6 background diabetic retinopathy 30.8 CRP ACE
7 cancer-associated retinopathy 30.8 SAG RCVRN
8 acquired immunodeficiency syndrome 30.6 CRP CD40LG CD4
9 macular retinal edema 30.5 MRAP ACE
10 scleritis 30.4 MRAP CRP
11 toxocariasis 30.4 MRAP CRP CD40LG
12 purpura 30.4 CRP CD40LG ACE
13 fuchs' heterochromic uveitis 30.2 MRAP ACE
14 boutonneuse fever 30.2 CS CD40LG
15 hypertensive retinopathy 30.2 CRP ACE
16 melanoma-associated retinopathy 30.2 TRPM1 SAG
17 pustulosis of palm and sole 30.1 MRAP CRP
18 interstitial keratitis 30.1 MRAP CD40LG
19 asymptomatic neurosyphilis 30.0 CD40LG CD4
20 patent foramen ovale 30.0 CRP CD40LG ACE
21 cholesterol embolism 30.0 CRP ACE
22 secondary syphilis 30.0 CD40LG CD4
23 subacute bacterial endocarditis 29.9 CRP CD40LG
24 rocky mountain spotted fever 29.9 CS CD40LG
25 enthesopathy 29.9 MRAP CRP
26 cat-scratch disease 29.9 CS CRP CD40LG CD4 ACE
27 spondyloarthropathy 1 29.8 MRAP CRP CD40LG
28 chickenpox 29.8 CRP CD40LG CD4
29 tolosa-hunt syndrome 29.8 CRP ACE
30 cysticercosis 29.8 CD40LG CD4
31 eye disease 29.8 SAG RCVRN MRAP CRP CD40LG CD4
32 congenital toxoplasmosis 29.8 CD40LG CD4
33 interstitial nephritis 29.8 CRP CD40LG ACE
34 anterior scleritis 29.8 MRAP CRP
35 pulmonary embolism 29.8 CRP CD40LG ACE
36 coccidioidomycosis 29.8 CD40LG CD4
37 intracranial embolism 29.8 CRP ACE
38 retinal vasculitis 29.7 SAG MRAP CD40LG CD4 ACE
39 polyneuropathy 29.7 CRP CD40LG ACE
40 bartonellosis 29.7 CS CRP CD40LG CD4
41 granulomatous angiitis 29.7 CRP ACE
42 interval angle-closure glaucoma 29.7 RCVRN CRP
43 posterior scleritis 29.6 MRAP CRP ACE
44 acute retinal necrosis syndrome 29.6 MRAP CD40LG CD4
45 ebola hemorrhagic fever 29.6 CD40LG CD4
46 focal chorioretinitis 29.6 SAG CD40LG
47 erysipelas 29.6 CRP CD40LG
48 papilledema 29.5 CRP CD40LG CD4 ACE
49 ecthyma 29.5 CRP CD40LG
50 ocular tuberculosis 29.5 MRAP CD4 ACE
51 cerebral atherosclerosis 29.5 CRP ACE
52 klebsiella pneumonia 29.5 CRP CD40LG
53 bacillary angiomatosis 29.5 CS CD40LG CD4
54 cellulitis 29.5 CRP CD40LG CD4
55 temporal arteritis 29.5 CRP CD40LG CD4
56 severe acute respiratory syndrome 29.5 CRP CD40LG ACE
57 maxillary sinusitis 29.5 CRP CD40LG
58 aortic valve insufficiency 29.5 MRAP CRP ACE
59 herpes zoster 29.5 CRP CD40LG CD4
60 croup 29.5 CRP CD40LG
61 multiple cranial nerve palsy 29.4 CRP ACE
62 latent syphilis 29.4 CD40LG CD4
63 generalized atherosclerosis 29.4 CRP ACE
64 epididymo-orchitis 29.4 MRAP CRP
65 portal hypertension 29.4 CD40LG CD4 ACE
66 mononeuropathy 29.4 CRP CD40LG
67 nocardiosis 29.4 CRP CD4
68 optic papillitis 29.3 MRAP CRP CD40LG CD4 ACE
69 good syndrome 29.3 CRP CD40LG CD4
70 granulomatosis with polyangiitis 29.3 CRP CD40LG CD4
71 tuberculoid leprosy 29.3 CD40LG CD4
72 lipoprotein quantitative trait locus 29.3 CRP CD40LG CD4 ACE
73 optic nerve disease 29.3 DPYSL5 CRP CD40LG CD4 ACE
74 rapidly progressive glomerulonephritis 29.3 CRP CD40LG
75 bell's palsy 29.3 CD40LG CD4
76 chronic meningitis 29.3 CRP CD40LG CD4
77 miliary tuberculosis 29.3 CRP CD40LG CD4
78 bacterial infectious disease 29.3 CRP CD40LG CD4
79 mucormycosis 29.3 CRP CD4
80 meningoencephalitis 29.2 CRP CD40LG CD4
81 giardiasis 29.2 CD40LG CD4
82 syphilis 29.2 MRAP CRP CD40LG CD4 ACE
83 mononeuritis multiplex 29.2 CRP CD40LG CD4
84 raynaud disease 29.2 CRP CD40LG ACE
85 diabetes mellitus, type i 29.2 CRP CD40LG CD4 ACE
86 hypersensitivity vasculitis 29.2 CRP CD40LG ACE
87 congenital syphilis 29.2 CD40LG CD4
88 intermittent claudication 29.1 CRP CD40LG ACE
89 hypopyon 29.1 MRAP CRP CD4
90 iridocyclitis 29.1 MRAP CRP CD40LG CD4 ACE
91 central nervous system vasculitis 29.1 CRP CD40LG CD4
92 vascular disease 29.1 CRP CD40LG CD4 ACE
93 sporotrichosis 29.1 CD40LG CD4
94 exanthem 29.1 CRP CD40LG CD4 ACE
95 kawasaki disease 29.1 CRP CD40LG CD4
96 babesiosis 29.1 CD40LG CD4
97 chlamydia pneumonia 29.0 CRP CD40LG CD4
98 iritis 29.0 MRAP CRP CD40LG CD4 ACE
99 pneumocystosis 29.0 CRP CD40LG CD4
100 chorioretinitis 29.0 SAG MRAP CD40LG CD4 ACE
101 cranial nerve palsy 29.0 CRP CD40LG CD4 ACE
102 chronic recurrent multifocal osteomyelitis 29.0 MRAP CRP
103 choroiditis 28.9 SAG MRAP CD40LG CD4 ACE
104 abdominal tuberculosis 28.9 CRP CD40LG CD4
105 xerophthalmia 28.9 CRP CD40LG CD4
106 orchitis 28.9 CRP CD40LG CD4
107 severe cutaneous adverse reaction 28.9 CRP CD40LG CD4
108 facial paralysis 28.9 CRP CD40LG CD4 ACE
109 blood coagulation disease 28.9 CRP CD40LG CD4
110 cytomegalovirus retinitis 28.8 CD40LG CD4
111 systemic scleroderma 28.8 CRP CD40LG CD4 ACE
112 pancytopenia 28.8 CRP CD40LG CD4 ACE
113 neurosarcoidosis 28.8 CRP CD4 ACE
114 panuveitis 28.7 SAG MRAP CRP CD40LG CD4 ACE
115 heart disease 28.7 CS CRP CD40LG CD4 ACE
116 vein disease 28.7 CRP CD40LG CD4 ACE
117 celiac disease 1 28.7 CRP CD40LG CD4
118 cerebritis 28.7 CRP CD40LG CD4
119 mastoiditis 28.7 CRP CD40LG CD4
120 hypertension, essential 28.7 SAG CRP CD40LG CD4 ACE
121 duodenitis 28.7 CRP CD40LG CD4
122 polyclonal hypergammaglobulinemia 28.7 CRP CD40LG CD4
123 parotitis 28.7 CRP CD40LG CD4
124 hantavirus hemorrhagic fever with renal syndrome 28.7 CRP CD40LG CD4
125 dysentery 28.6 CRP CD40LG CD4
126 bacterial pneumonia 28.6 CRP CD40LG CD4
127 parasitic protozoa infectious disease 28.6 CRP CD40LG CD4
128 sarcoidosis 1 28.6 MRAP CRP CD40LG CD4 ACE
129 pericardial effusion 28.6 CRP CD40LG CD4 ACE
130 acute cystitis 28.6 CRP CD40LG CD4 ACE
131 leukocyte disease 28.6 CRP CD40LG CD4
132 respiratory failure 28.6 CRP CD40LG CD4 ACE
133 igg4-related disease 28.6 CRP CD4
134 endophthalmitis 28.5 SAG MRAP CRP CD4
135 epidemic typhus 28.5 CS CRP CD40LG CD4
136 pericarditis 28.5 CRP CD40LG CD4 ACE
137 connective tissue disease 28.4 MRAP CRP CD40LG CD4 ACE
138 coccidiosis 28.2 MRAP CRP CD40LG CD4
139 bone inflammation disease 28.2 MRAP CRP CD40LG CD4
140 retinitis pigmentosa 28.1 TRPM1 SAG RCVRN MRAP CD40LG CD4
141 behcet syndrome 28.0 SAG MRAP CRP CD40LG CD4 ACE
142 peripheral nervous system disease 27.9 MRAP DPYSL5 CRP CD40LG CD4 ACE
143 uveal disease 27.6 SAG MRAP CRP CD40LG CD4 ACE
144 retinitis pigmentosa 3 12.6
145 retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities 12.6
146 doyne honeycomb retinal dystrophy 12.6
147 retinitis pigmentosa 12 12.6
148 retinitis pigmentosa 27 12.6
149 retinitis pigmentosa 7 12.6
150 retinitis pigmentosa 50 12.5
151 retinitis pigmentosa 2 12.5
152 retinitis pigmentosa 10 12.5
153 retinitis pigmentosa 1 12.5
154 retinitis pigmentosa 11 12.5
155 retinitis pigmentosa 41 12.5
156 retinitis pigmentosa 67 12.5
157 retinitis pigmentosa 9 12.5
158 vasculopathy, retinal, with cerebral leukodystrophy 12.5
159 retinitis pigmentosa 14 12.5
160 retinitis pigmentosa 38 12.5
161 late-onset retinal degeneration 12.5
162 retinitis pigmentosa 46 12.5
163 retinitis pigmentosa 57 12.5
164 retinitis pigmentosa 13 12.5
165 retinitis pigmentosa 17 12.5
166 retinitis pigmentosa 28 12.5
167 retinitis pigmentosa 25 12.5
168 retinitis pigmentosa 18 12.5
169 retinitis pigmentosa 19 12.5
170 retinitis pigmentosa 30 12.5
171 retinitis pigmentosa 26 12.5
172 retinitis pigmentosa 20 12.5
173 retinitis pigmentosa 33 12.5
174 retinitis pigmentosa 40 12.5
175 retinitis pigmentosa 31 12.5
176 retinitis pigmentosa 36 12.5
177 retinitis pigmentosa 35 12.5
178 retinitis pigmentosa 69 12.5
179 retinitis pigmentosa 43 12.5
180 retinitis pigmentosa 23 12.5
181 retinitis pigmentosa 37 12.5
182 retinitis pigmentosa 42 12.5
183 retinitis pigmentosa 45 12.5
184 retinitis pigmentosa 39 12.5
185 retinitis pigmentosa 55 12.5
186 retinitis pigmentosa 58 12.5
187 retinitis pigmentosa 54 12.5
188 retinitis pigmentosa 51 12.5
189 retinitis pigmentosa 48 12.5
190 retinitis pigmentosa 62 12.5
191 retinitis pigmentosa 49 12.5
192 retinitis pigmentosa 47 12.5
193 retinitis pigmentosa 44 12.5
194 retinitis pigmentosa 60 12.5
195 retinitis pigmentosa 61 12.5
196 retinal arteries, tortuosity of 12.5
197 neuropathy, ataxia, and retinitis pigmentosa 12.5
198 retinitis pigmentosa 59 12.5
199 retinitis pigmentosa 66 12.5
200 retinitis pigmentosa 75 12.5
201 retinitis pigmentosa 70 12.5
202 retinitis pigmentosa 82 with or without situs inversus 12.5
203 retinitis pigmentosa 68 12.5
204 bothnia retinal dystrophy 12.5
205 retinal dystrophy, iris coloboma, and comedogenic acne syndrome 12.5
206 retinitis pigmentosa 71 12.5
207 retinitis pigmentosa 72 12.5
208 retinitis pigmentosa 73 12.5
209 retinitis pigmentosa 74 12.5
210 retinitis pigmentosa 56 12.5
211 infantile cerebellar-retinal degeneration 12.5
212 retinitis pigmentosa 77 12.5
213 posterior column ataxia with retinitis pigmentosa 12.5
214 retinal arterial macroaneurysm with supravalvular pulmonic stenosis 12.5
215 retinal cone dystrophy 3b 12.4
216 polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract 12.4
217 retinitis pigmentosa 6 12.4
218 retinal dystrophy, juvenile cataracts, and short stature syndrome 12.4
219 retinitis pigmentosa 24 12.4
220 retinitis pigmentosa 32 12.4
221 retinitis pigmentosa 34 12.4
222 retinitis pigmentosa 22 12.4
223 retinitis pigmentosa 29 12.4
224 retinitis pigmentosa 83 12.4
225 retinitis pigmentosa 86 12.4
226 retinitis pigmentosa with or without skeletal anomalies 12.4
227 retinal degeneration with nanophthalmos, cystic macular degeneration, and angle closure glaucoma 12.4
228 retinitis pigmentosa 63 12.4
229 retinitis pigmentosa, late-adult onset 12.4
230 retinitis pigmentosa 87 with choroidal involvement 12.4
231 retinitis pigmentosa 81 12.4
232 retinal dystrophy with or without extraocular anomalies 12.4
233 retinitis pigmentosa-deafness syndrome 12.4
234 retinitis pigmentosa, x-linked, and sinorespiratory infections, with or without deafness 12.4
235 recurrent idiopathic neuroretinitis 12.4
236 retinitis pigmentosa 78 12.4
237 retinitis pigmentosa 76 12.4
238 retinitis pigmentosa 79 12.4
239 retinitis pigmentosa 85 12.4
240 retinitis pigmentosa 88 12.4
241 mental retardation, truncal obesity, retinal dystrophy, and micropenis syndrome 12.4
242 retinitis pigmentosa 80 12.4
243 optic disc anomalies with retinal and/or macular dystrophy 12.3
244 short stature, hearing loss, retinitis pigmentosa, and distinctive facies 12.3
245 retinitis pigmentosa, y-linked 12.3
246 retinal cone dystrophy 3a 12.3
247 retinal cone dystrophy 4 12.3
248 macular dystrophy, retinal, 2 12.3
249 reticular dystrophy of retinal pigment epithelium 12.3
250 hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration 12.3
251 retinal dystrophy with or without macular staphyloma 12.3
252 intellectual developmental disorder and retinitis pigmentosa 12.3
253 retinal dystrophy and obesity 12.3
254 retinitis pigmentosa and erythrocytic microcytosis 12.3
255 retinal perforation 12.3
256 cone-rod dystrophy 2 12.3
257 macular dystrophy, retinal, 1, north carolina type 12.3
258 hereditary retinal dystrophy 12.3
259 uncombable hair, retinal pigmentary dystrophy, dental anomalies, and brachydactyly 12.2
260 retinal dystrophy, reticular pigmentary, of posterior pole 12.2
261 retinal dystrophy with leukodystrophy 12.2
262 irvan syndrome 12.2
263 peripheral retinal degeneration 12.2
264 severe early-childhood-onset retinal dystrophy 12.2
265 usher syndrome 12.2
266 retinal cancer 12.2
267 retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome 12.2
268 corneal hypesthesia with retinal abnormalities, sensorineural deafness, unusual facies, persistent ductus arteriosus, and mental retardation 12.2
269 retinal cone dystrophy 1 12.1
270 gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy 12.1
271 vitreoretinopathy, neovascular inflammatory 12.1
272 inherited retinal disorder 12.1
273 transient retinal arterial occlusion 12.1
274 retinal drusen 12.1
275 retinal dystrophy and iris coloboma with or without congenital cataract 12.1
276 partial arterial retinal occlusion 12.1
277 spastic tetraplegia-retinitis pigmentosa-intellectual disability syndrome 12.1
278 senior-loken syndrome 1 12.1
279 leber plus disease 12.1
280 muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus 12.1
281 histoplasmosis retinitis 12.1
282 leber congenital amaurosis 14 12.1
283 retinal telangiectasia 12.1
284 abnormal retinal correspondence 12.1
285 retinal hemangioblastoma 12.1
286 macular dystrophy, patterned, 3 12.1
287 cone-rod dystrophy 6 12.1
288 retinal lattice degeneration 12.1
289 usher syndrome, type i 12.1
290 retinal ciliopathy due to mutation in the retinitis pigmentosa-1 gene 12.1
291 reese retinal dysplasia 12.1
292 leber congenital amaurosis 4 12.1
293 encephalopathy with intracranial calcification, growth hormone deficiency, microcephaly, and retinal degeneration 12.1
294 spastic quadriplegia, retinitis pigmentosa, and mental retardation 12.1
295 macular dystrophy, retinal, 3 12.1
296 cone-rod dystrophy 16 12.1
297 short-rib thoracic dysplasia 9 with or without polydactyly 12.1
298 syndromic inherited retinal disorder 12.0
299 retinal dysplasia, primary 12.0
300 congenital retinal arteriovenous communication 12.0
301 retinal aplasia 12.0
302 deafness, cataract, retinitis pigmentosa, and sperm abnormalities 12.0
303 nonsyndromic retinitis pigmentosa 12.0
304 combined hamartoma of the retina and retinal pigment epithelium 12.0
305 macular dystrophy, patterned, 1 12.0
306 leber congenital amaurosis / early-onset severe retinal dystrophy 12.0
307 rpe65-related leber congenital amaurosis / early-onset severe retinal dystrophy 12.0
308 retinal ciliopathy 12.0
309 leber congenital amaurosis 13 12.0
310 stickler syndrome, type i, nonsyndromic ocular 12.0
311 retinal venous beading 12.0
312 rare retinal disorder 12.0
313 lattice degeneration of retina leading to retinal detachment 12.0
314 retinal telangiectasia and hypogammaglobulinemia 12.0
315 retinitis pigmentosa inversa with deafness 12.0
316 microcephaly, retinitis pigmentosa, and sutural cataract 12.0
317 sensorineural hearing loss, retinal pigment epithelium lesions, discolored teeth 12.0
318 skeletal dysplasia, rhizomelic, with retinitis pigmentosa 12.0
319 rare retinal vasculopathy 12.0
320 leber congenital amaurosis 3 12.0
321 retinitis pigmentosa, deafness, mental retardation, and hypogonadism 12.0
322 cobblestone retinal degeneration 12.0
323 partial of retinal vein occlusion 12.0
324 osteochondrodysplatic nanism-deafness-retinitis pigmentosa syndrome 12.0
325 leber congenital amaurosis 1 12.0
326 persistent hyperplastic primary vitreous, autosomal recessive 12.0
327 usher syndrome, type iia 11.9
328 orofaciodigital syndrome ix 11.9
329 retinal melanoma 11.9
330 aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome 11.9
331 fundus albipunctatus 11.9
332 retinoblastoma 11.9
333 rhyns syndrome 11.9
334 microphthalmia, isolated 5 11.9
335 rhizomelic dysplasia, scoliosis, and retinitis pigmentosa 11.9
336 senile reticular retinal degeneration 11.9
337 hole retinal cyst 11.9
338 retinal dystrophies primarily involving bruch's membrane 11.9
339 cystoid macular retinal degeneration 11.9
340 hypogonadotropic hypogonadism-retinitis pigmentosa syndrome 11.9
341 pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa 11.9
342 knobloch syndrome 11.9
343 cone-rod dystrophy 15 11.9
344 microcephaly with or without chorioretinopathy, lymphedema, or mental retardation 11.9
345 microphthalmia, syndromic 5 11.9
346 aortic arch interruption, facial palsy, and retinal coloboma 11.9
347 diverticulosis of bowel, hernia, and retinal detachment 11.9
348 microphthalmia with hyperopia, retinal degeneration, macrophakia, and dental anomalies 11.9
349 pallidal degeneration, progressive, with retinitis pigmentosa 11.9
350 retinal degeneration and epilepsy 11.9
351 dystrophies primarily involving the retinal pigment epithelium 11.9
352 retinal dystrophy in systemic or cerebroretinal lipidoses 11.9
353 dwarfism deafness retinitis pigmentosa 11.9
354 retinal dysplasia x-linked 11.9
355 genetic central nervous system and retinal vascular disease 11.9
356 retinal ciliopathy due to mutation in nephronophthisis gene 11.9
357 retinal ciliopathy due to mutation in bardet-biedl gene 11.9
358 retinal ciliopathy due to mutation in the rpgr gene 11.9
359 retinal ciliopathy due to mutation in the rpgrip gene 11.9
360 retinal ciliopathy due to mutation in usher gene 11.9
361 microcephaly-cleft palate-abnormal retinal pigmentation syndrome 11.9
362 autosomal recessive leukoencephalopathy-ischemic stroke-retinitis pigmentosa syndrome 11.9
363 x-linked intellectual disability-limb spasticity-retinal dystrophy-diabetes insipidus syndrome 11.9
364 rare central nervous system and retinal vascular disease 11.9
365 retinal capillary malformation 11.9
366 isolated progressive inherited retinal disorder 11.9
367 isolated stationary inherited retinal disorder 11.9
368 rare genetic retinal vasculopathy 11.9
369 rare genetic retinal disorder 11.9
370 isolated inherited retinal disorder 11.9
371 retinopathy, pericentral pigmentary, autosomal recessive 11.8
372 spastic paraplegia 15, autosomal recessive 11.8
373 stargardt disease 1 11.8
374 angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps 11.8
375 knobloch syndrome 1 11.8
376 vitreoretinochoroidopathy 11.8
377 exudative vitreoretinopathy 11.8
378 cone-rod dystrophy 21 11.8
379 spinocerebellar ataxia 7 11.8
380 walker-warburg syndrome 11.8
381 roifman syndrome 11.7
382 spastic paraplegia 15 11.7
383 chromosome xp11.3 deletion syndrome 11.7
384 cone dystrophy 3 11.7
385 cone-rod dystrophy 7 11.7
386 cone-rod dystrophy 9 11.7
387 retinochoroidal coloboma 11.7
388 retinoschisis 1, x-linked, juvenile 11.7
389 persistent hyperplastic primary vitreous 11.7
390 muscular dystrophy-dystroglycanopathy , type a, 1 11.7
391 cone dystrophy 11.7
392 enhanced s-cone syndrome 11.7
393 oculoauricular syndrome 11.7
394 patterned macular dystrophy 11.6
395 optic neuritis 11.6
396 oliver-mcfarlane syndrome 11.6
397 aldred syndrome 11.6
398 leber congenital amaurosis 15 11.6
399 retinopathy, pigmentary, and mental retardation 11.6
400 usher syndrome, type id 11.6
401 brain small vessel disease 1 with or without ocular anomalies 11.6
402 basal laminar drusen 11.6
403 usher syndrome, type ic 11.6
404 pigmented paravenous chorioretinal atrophy 11.6
405 cerebroretinal microangiopathy with calcifications and cysts 1 11.6
406 stargardt disease 11.6
407 familial drusen 11.6
408 bestrophinopathy, autosomal recessive 11.6
409 macular dystrophy, vitelliform, 2 11.6
410 exudative vitreoretinopathy 2, x-linked 11.5
411 usher syndrome, type iic 11.5
412 von hippel-lindau syndrome 11.5
413 usher syndrome, type iiia 11.5
414 bietti crystalline corneoretinal dystrophy 11.5
415 macular telangiectasia type 2 11.5
416 refsum disease, classic 11.5
417 leber congenital amaurosis 2 11.5
418 spastic ataxia, charlevoix-saguenay type 11.5
419 choroideremia 11.5
420 ramos arroyo clark syndrome 11.5
421 trnt1 deficiency 11.5
422 sorsby fundus dystrophy 11.5
423 pattern dystrophy 11.5
424 leber congenital amaurosis 8 11.5
425 leber congenital amaurosis 7 11.5
426 leber congenital amaurosis 11 11.5
427 choroidal dystrophy, central areolar, 1 11.5
428 wagner vitreoretinopathy 11.5
429 spondylometaphyseal dysplasia, axial 11.5
430 usher syndrome, type if 11.5
431 leber congenital amaurosis 6 11.5
432 retinopathy, pericentral pigmentary, dominant 11.5
433 aland island eye disease 11.5
434 usher syndrome, type iid 11.5
435 papillorenal syndrome 11.5
436 exudative vitreoretinopathy 3 11.5
437 cone-rod dystrophy 3 11.4
438 idiopathic macular telangiectasia type 1 11.4
439 stickler syndrome 11.4
440 cone-rod dystrophy, x-linked, 1 11.4
441 exudative vitreoretinopathy 5 11.4
442 idiopathic macular telangiectasia type 3 11.4
443 cone-rod dystrophy 1 11.4
444 flynn-aird syndrome 11.4
445 vitelliform macular dystrophy 11.4
446 vitreoretinal degeneration, snowflake type 11.4
447 usher syndrome, type ig 11.4
448 joubert syndrome 1 11.4
449 col4a1-related familial vascular leukoencephalopathy 11.4
450 autoimmune retinopathy 11.4
451 oguchi disease 11.4
452 abetalipoproteinemia 11.4
453 usher syndrome type 2 11.4
454 bardet-biedl syndrome 11.4
455 norrie disease 11.4
456 night blindness, congenital stationary, type 1e 11.4
457 kniest dysplasia 11.4
458 night blindness, congenital stationary, type1i 11.4
459 neurodegeneration with brain iron accumulation 11.4
460 cone-rod dystrophy, x-linked, 3 11.4
461 ceroid lipofuscinosis, neuronal, 11 11.4
462 macular dystrophy, vitelliform, 5 11.4
463 occult macular dystrophy 11.4
464 syndromic rod-cone dystrophy 11.4
465 macular dystrophy, vitelliform, 3 11.4
466 kuhnt-junius degeneration 11.4
467 leber congenital amaurosis 10 11.4
468 jalili syndrome 11.4
469 fleck retina, familial benign 11.4
470 usher syndrome, type iiib 11.4
471 usher syndrome, type ij 11.4
472 joubert syndrome 3 11.3
473 night blindness 11.3
474 cockayne syndrome 11.3
475 pseudoretinitis pigmentosa 11.3
476 cranioectodermal dysplasia 1 11.3
477 neurodegeneration with brain iron accumulation 1 11.3
478 vascular hyalinosis 11.3
479 blessig's cysts 11.3
480 laurence-moon syndrome 11.3
481 cone-rod dystrophy 5 11.3
482 newfoundland rod-cone dystrophy 11.3
483 cone-rod dystrophy 13 11.3
484 cone-rod dystrophy 10 11.3
485 choroidal dystrophy, central areolar 2 11.3
486 arima syndrome 11.3
487 cone-rod dystrophy 11 11.3
488 cone-rod dystrophy 12 11.3
489 cone-rod dystrophy 18 11.3
490 cone-rod dystrophy 19 11.3
491 cone-rod dystrophy 20 11.3
492 ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome 11.3
493 peroxisome biogenesis disorder 1b 11.3
494 macular dystrophy, patterned, 2 11.3
495 exudative vitreoretinopathy 6 11.3
496 exudative vitreoretinopathy 7 11.3
497 cone-rod dystrophy and hearing loss 2 11.3
498 nephronophthisis 11.3
499 optic atrophy 1 11.3
500 best vitelliform macular dystrophy 11.3
501 bardet-biedl syndrome 1 11.3
502 isolated ectopia lentis 11.3
503 retinitis pigmentosa 84 11.3
504 wagner syndrome 11.2
505 bardet-biedl syndrome 2 11.2
506 spondyloepimetaphyseal dysplasia, strudwick type 11.2
507 solar retinopathy 11.2
508 exudative vitreoretinopathy 4 11.2
509 macular degeneration, age-related, 2 11.2
510 alstrom syndrome 11.2
511 bardet-biedl syndrome 3 11.2
512 ataxia with vitamin e deficiency 11.2
513 susac syndrome 11.2
514 stickler syndrome, type i 11.2
515 spondyloepiphyseal dysplasia congenita 11.2
516 spondyloocular syndrome 11.2
517 poretti-boltshauser syndrome 11.2
518 bardet-biedl syndrome 4 11.2
519 preretinal fibrosis 11.2
520 sveinsson chorioretinal atrophy 11.2
521 stargardt disease 4 11.2
522 cranioectodermal dysplasia 4 11.2
523 sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay 11.2
524 perching syndrome 11.2
525 retina lymphoma 11.2
526 achromatopsia 11.2
527 vasoproliferative tumor of the retina 11.2
528 shaken baby syndrome 11.2
529 grouped pigmentation of the retina 11.2
530 frenkel russe syndrome 11.2
531 ghose sachdev kumar syndrome 11.2
532 melanoma, uveal 11.2
533 microcephaly 11.2
534 degenerative myopia 11.2
535 intraocular lymphoma 11.2
536 leber optic atrophy 11.2
537 macular dystrophy, concentric annular 11.1
538 usher syndrome, type ih 11.1
539 usher syndrome, type ik 11.1
540 acute posterior multifocal placoid pigment epitheliopathy 11.1
541 vitreoretinal degeneration 11.1
542 pseudoxanthoma elasticum 11.1
543 acute zonal occult outer retinopathy 11.1
544 facioscapulohumeral muscular dystrophy 1 11.1
545 night blindness, congenital stationary, autosomal dominant 2 11.1
546 aceruloplasminemia 11.1
547 oguchi disease 1 11.1
548 stargardt disease 3 11.1
549 cohen syndrome 11.1
550 nephronophthisis 1 11.1
551 night blindness, congenital stationary, type 2a 11.1
552 blue cone monochromacy 11.1
553 diabetes and deafness, maternally inherited 11.1
554 sjogren-larsson syndrome 11.1
555 prolonged electroretinal response suppression 11.1
556 mevalonic aciduria 11.1
557 pseudopapilledema 11.1
558 osteoporosis-pseudoglioma syndrome 11.1
559 chorioretinal atrophy, progressive bifocal 11.1
560 bardet-biedl syndrome 6 11.1
561 nerve fibre bundle defect 11.1
562 spinocerebellar ataxia 2 11.1
563 donnai-barrow syndrome 11.1
564 mucolipidosis iv 11.1
565 aicardi syndrome 11.1
566 neuropathy, hereditary, with or without age-related macular degeneration 11.1
567 joubert syndrome 4 11.1
568 bardet-biedl syndrome 5 11.1
569 bardet-biedl syndrome 8 11.1
570 bardet-biedl syndrome 10 11.1
571 bardet-biedl syndrome 12 11.1
572 asphyxiating thoracic dystrophy 11.1
573 ocular melanoma 11.1
574 optic atrophy 3, autosomal dominant 11.1
575 thiamine-responsive megaloblastic anemia syndrome 11.1
576 ceroid lipofuscinosis, neuronal, 6 11.1
577 senior-loken syndrome 4 11.1
578 cone-rod synaptic disorder, congenital nonprogressive 11.1
579 neurodevelopmental disorder with spastic diplegia and visual defects 11.1
580 hypobetalipoproteinemia, familial, 1 11.1
581 bardet-biedl syndrome 7 11.1
582 bardet-biedl syndrome 17 11.1
583 bardet-biedl syndrome 21 11.1
584 zellweger syndrome 11.1
585 adams-oliver syndrome 1 11.1
586 spinocerebellar ataxia 1 11.1
587 ceroid lipofuscinosis, neuronal, 4a, autosomal recessive 11.1
588 epiphyseal dysplasia, microcephaly, and nystagmus 11.1
589 gapo syndrome 11.1
590 muscular dystrophy-dystroglycanopathy , type a, 3 11.1
591 ceroid lipofuscinosis, neuronal, 1 11.1
592 gurrieri syndrome 11.1
593 hypotrichosis, congenital, with juvenile macular dystrophy 11.1
594 joubert syndrome 6 11.1
595 macular degeneration, age-related, 4 11.1
596 joubert syndrome 9 11.1
597 joubert syndrome 8 11.1
598 cone dystrophy 4 11.1
599 senior-loken syndrome 7 11.1
600 macular degeneration, age-related, 14 11.1
601 macular degeneration, age-related, 15 11.1
602 bardet-biedl syndrome 16 11.1
603 senior-loken syndrome 8 11.1
604 night blindness, congenital stationary, type 1g 11.1
605 borderline glaucoma 11.1
606 fukuyama type muscular dystrophy 11.1
607 congenital disorder of glycosylation, type ia 11.1
608 macular dystrophy, vitelliform, 4 11.1
609 thyrocerebroretinal syndrome 11.0
610 tietz albinism-deafness syndrome 11.0
611 microcephaly and chorioretinopathy, autosomal recessive, 3 11.0
612 usher syndrome, type iv 11.0
613 alezzandrini syndrome 11.0
614 vitreoretinopathy 11.0
615 epiphyseal dysplasia, multiple, with myopia and conductive deafness 10.9
616 foveal hypoplasia 1 10.9
617 peroxisome biogenesis disorder 2b 10.9
618 ectopia lentis et pupillae 10.9
619 heimler syndrome 1 10.9
620 night blindness, congenital stationary, type 1b 10.9
621 peroxisome biogenesis disorder 3b 10.9
622 spondylocarpotarsal synostosis syndrome 10.9
623 night blindness, congenital stationary, type 1a 10.9
624 oculoectodermal syndrome 10.9
625 albinism, oculocutaneous, type ib 10.9
626 microphthalmia, syndromic 6 10.9
627 joubert syndrome 2 10.9
628 foveal hypoplasia 2 10.9
629 joubert syndrome 5 10.9
630 cavitary optic disc anomalies 10.9
631 nephronophthisis 12 10.9
632 cranioectodermal dysplasia 3 10.9
633 brittle cornea syndrome 2 10.9
634 peroxisome biogenesis disorder 4b 10.9
635 peroxisome biogenesis disorder 5b 10.9
636 peroxisome biogenesis disorder 6b 10.9
637 peroxisome biogenesis disorder 7b 10.9
638 peroxisome biogenesis disorder 11b 10.9
639 joubert syndrome 21 10.9
640 night blindness, congenital stationary, type 1h 10.9
641 cone-rod dystrophy and hearing loss 1 10.9
642 joubert syndrome 33 10.9
643 mitochondrial complex v deficiency, nuclear type 5 10.9
644 joubert syndrome 35 10.9
645 neurodevelopmental disorder with visual defects and brain anomalies 10.9
646 usher syndrome, type 1m 10.9
647 cerebellar hyplasia/atrophy, epilepsy, and global developmental delay 10.9
648 ayazi syndrome 10.9
649 cerebellar hypoplasia tapetoretinal degeneration 10.9
650 familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis 10.9
651 col4a1-related brain small-vessel disease 10.9
652 autosomal recessive chorioretinopathy-microcephaly syndrome 10.9
653 bile acid synthesis defect, congenital, 4 10.9
654 lethal congenital contracture syndrome 5 10.9
655 ruvalcaba churesigaew myhre syndrome 10.9
656 anemia, congenital dyserythropoietic, type iii 10.8
657 coloboma of optic nerve 10.8
658 cockayne syndrome b 10.8
659 hypoparathyroidism, sensorineural deafness, and renal disease 10.8
660 macular dystrophy, vitelliform, 1 10.8
661 microspherophakia-metaphyseal dysplasia 10.8
662 ceroid lipofuscinosis, neuronal, 4b, autosomal dominant 10.8
663 otodental dysplasia 10.8
664 glaucoma 1, open angle, p 10.8
665 acrocallosal syndrome 10.8
666 gillespie syndrome 10.8
667 cerebrotendinous xanthomatosis 10.8
668 apparent mineralocorticoid excess 10.8
669 proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome 10.8
670 ermine phenotype 10.8
671 hypertrichosis, congenital anterior cervical, with peripheral sensory and motor neuropathy 10.8
672 baraitser-winter syndrome 1 10.8
673 chylomicron retention disease 10.8
674 hsd10 mitochondrial disease 10.8
675 albinism, ocular, with late-onset sensorineural deafness 10.8
676 joubert syndrome 10 10.8
677 macular degeneration, x-linked atrophic 10.8
678 bornholm eye disease 10.8
679 spastic paraparesis and deafness 10.8
680 cerebellar ataxia, cayman type 10.8
681 stickler syndrome, type ii 10.8
682 lethal congenital contracture syndrome 2 10.8
683 spondylometaphyseal dysplasia with cone-rod dystrophy 10.8
684 pierson syndrome 10.8
685 senior-loken syndrome 5 10.8
686 macular degeneration, age-related, 7 10.8
687 senior-loken syndrome 6 10.8
688 night blindness, congenital stationary, autosomal dominant 3 10.8
689 night blindness, congenital stationary, autosomal dominant 1 10.8
690 optic atrophy 5 10.8
691 macular degeneration, age-related, 9 10.8
692 macular degeneration, age-related, 10 10.8
693 joubert syndrome 7 10.8
694 macular degeneration, age-related, 11 10.8
695 nephronophthisis-like nephropathy 1 10.8
696 night blindness, congenital stationary, type 1c 10.8
697 oguchi disease 2 10.8
698 cranioectodermal dysplasia 2 10.8
699 macular degeneration, age-related, 6 10.8
700 macular degeneration, age-related, 5 10.8
701 macular degeneration, age-related, 8 10.8
702 macular degeneration, age-related, 12 10.8
703 night blindness, congenital stationary, type 1d 10.8
704 stickler syndrome, type iv 10.8
705 joubert syndrome 13 10.8
706 meckel syndrome, type 10 10.8
707 stickler syndrome, type v 10.8
708 myopia, high, with cataract and vitreoretinal degeneration 10.8
709 alpha-methylacyl-coa racemase deficiency 10.8
710 joubert syndrome 15 10.8
711 joubert syndrome 16 10.8
712 leukoencephalopathy, brain calcifications, and cysts 10.8
713 joubert syndrome 17 10.8
714 joubert syndrome 18 10.8
715 nephronophthisis 15 10.8
716 peroxisome biogenesis disorder 8b 10.8
717 joubert syndrome 20 10.8
718 night blindness, congenital stationary, type 1f 10.8
719 muscular dystrophy-dystroglycanopathy , type a, 14 10.8
720 macular degeneration, age-related, 13 10.8
721 joubert syndrome 22 10.8
722 bardet-biedl syndrome 13 10.8
723 bardet-biedl syndrome 14 10.8
724 bardet-biedl syndrome 18 10.8
725 bardet-biedl syndrome 19 10.8
726 adams-oliver syndrome 5 10.8
727 macular dystrophy with central cone involvement 10.8
728 joubert syndrome 23 10.8
729 adams-oliver syndrome 6 10.8
730 heimler syndrome 2 10.8
731 senior-loken syndrome 9 10.8
732 joubert syndrome 24 10.8
733 joubert syndrome 25 10.8
734 joubert syndrome 26 10.8
735 bone marrow failure syndrome 3 10.8
736 bardet-biedl syndrome 20 10.8
737 joubert syndrome 27 10.8
738 joubert syndrome 28 10.8
739 anterior segment dysgenesis 8 10.8
740 cerebroretinal microangiopathy with calcifications and cysts 2 10.8
741 meckel syndrome 13 10.8
742 joubert syndrome 30 10.8
743 joubert syndrome 32 10.8
744 joubert syndrome 31 10.8
745 leber congenital amaurosis with early-onset deafness 10.8
746 jaberi-elahi syndrome 10.8
747 saul-wilson syndrome 10.8
748 cerebellar, ocular, craniofacial, and genital syndrome 10.8
749 joubert syndrome 36 10.8
750 liberfarb syndrome 10.8
751 arterial calcification of infancy 10.8
752 charcot-marie-tooth disease type 7 10.8
753 anatomical narrow angle borderline glaucoma 10.8
754 2-methyl-3-hydroxybutyric aciduria 10.8
755 refsum disease, infantile form 10.8
756 ring chromosome 17 10.8
757 spastic paraplegia 10 10.8
758 alg6-congenital disorder of glycosylation 10.8
759 vasculitis 10.7
760 aneurysm 10.7
761 vitreous detachment 10.7
762 intraocular pressure quantitative trait locus 10.7
763 eales disease 10.7
764 hyperglycemia 10.6
765 leber congenital amaurosis 5 10.6
766 leber congenital amaurosis 12 10.6
767 butterfly-shaped pigment dystrophy 10.6
768 familial retinoblastoma 10.6
769 congenital heart defects, hamartomas of tongue, and polysyndactyly 10.6
770 hemangioma 10.6
771 leber congenital amaurosis 9 10.6
772 strabismus 10.6
773 mechanical strabismus 10.6
774 leber congenital amaurosis 16 10.5
775 pathologic nystagmus 10.5
776 leber congenital amaurosis 17 10.5
777 open-angle glaucoma 10.5
778 ataxia and polyneuropathy, adult-onset 10.5
779 retinitis 10.5
780 myopic macular degeneration 10.5
781 fundus pulverulentus 10.5
782 branchiootic syndrome 1 10.5
783 migraine with or without aura 1 10.5
784 retinal detachment 10.5
785 uveitis 10.5
786 melioidosis 10.4
787 microvascular complications of diabetes 5 10.4
788 retinal vascular disease 10.4
789 pars planitis 10.4
790 histoplasmosis meningitis 10.4 CD40LG ACE
791 brawny scleritis 10.4 CD40LG ACE
792 alzheimer disease 10.4
793 neurofibromatosis 10.4
794 glaucoma, primary open angle 10.4
795 neuritis 10.4
796 cholera 10.4
797 autoimmune uveitis 10.4
798 ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus 10.4
799 thrombophilia 10.4
800 tuberous sclerosis 10.4
801 ocular hypertension 10.4
802 ciliopathy 10.4
803 carotid stenosis 10.4
804 arteriosclerosis 10.4
805 cytokine deficiency 10.4
806 3-methylglutaconic aciduria, type iii 10.4
807 posttransplant acute limbic encephalitis 10.4
808 atherosclerosis susceptibility 10.4
809 african tick-bite fever 10.4 CS CD40LG
810 pulmonary tuberculosis 10.4
811 yemenite deaf-blind hypopigmentation syndrome 10.4
812 lyme disease 10.4
813 autoimmune disease 10.4
814 48,xyyy 10.4
815 capillary hemangioma 10.4
816 hereditary optic neuropathy 10.4
817 papillomatosis, confluent and reticulated 10.4
818 hemangioblastoma 10.3
819 leukostasis 10.3
820 helix syndrome 10.3
821 rubeosis iridis 10.3
822 astrocytoma 10.3
823 la crosse encephalitis 10.3 DPYSL5 CD40LG
824 plexopathy 10.3 DPYSL5 CD40LG
825 pertussis 10.3
826 albinism 10.3
827 hypercholesterolemia, familial, 1 10.3
828 retinal ischemia 10.3
829 toxoplasmosis 10.3
830 kidney disease 10.3
831 autosomal recessive disease 10.3
832 familial adenomatous polyposis 10.3
833 sickle cell disease 10.3
834 amaurosis fugax 10.3
835 splenic abscess 10.3 CRP CD40LG
836 neuropathy 10.3
837 relapsing-remitting multiple sclerosis 10.3
838 head injury 10.3
839 acalculous cholecystitis 10.3 CRP CD40LG
840 melanoma, cutaneous malignant 10 10.3
841 keratopathy 10.3
842 cerebrovascular disease 10.3
843 epiglottitis 10.3 CRP CD40LG
844 viral laryngitis 10.3 CRP CD40LG
845 laryngitis 10.3 CRP CD40LG
846 kearns-sayre syndrome 10.3
847 arteriovenous malformation 10.3
848 sleep apnea 10.3
849 foster-kennedy syndrome 10.3
850 ornithosis 10.3 CRP CD40LG
851 late congenital syphilis 10.3 CRP CD40LG
852 aging 10.3
853 periodontal ehlers-danlos syndrome 10.3
854 glial tumor 10.3
855 critical illness polyneuropathy 10.3 CS CRP
856 bacterial conjunctivitis 10.3 CRP CD40LG
857 splenic infarction 10.3 CRP CD40LG
858 dermatitis, atopic 10.3
859 glioma 10.3
860 exophthalmos 10.2
861 muscular dystrophy 10.2
862 mediastinum teratoma 10.2 CRP ACE
863 vogt-koyanagi-harada disease 10.2
864 b-cell lymphoma 10.2
865 hydrops of gallbladder 10.2 CRP CD40LG
866 cavernous hemangioma 10.2
867 acute dacryoadenitis 10.2 CRP ACE
868 pyuria 10.2 CRP CD40LG
869 cardiac tuberculosis 10.2 CRP ACE
870 inclusion body myopathy with early-onset paget disease of bone with or without frontotemporal dementia 3 10.2 SAG CD40LG
871 scarlet fever 10.2 CRP CD40LG
872 endemic typhus 10.2 CS CRP
873 severe nonproliferative diabetic retinopathy 10.2
874 stargardt macular degeneration 10.2
875 gyrate atrophy of choroid and retina 10.2
876 sensorineural hearing loss 10.2
877 suppurative otitis media 10.2 CRP CD40LG
878 silent myocardial infarction 10.2 CRP ACE
879 mycobacterium tuberculosis 1 10.2
880 myelitis 10.2
881 arteries, anomalies of 10.2
882 insulin-like growth factor i 10.2
883 eclampsia 10.2
884 adenoma 10.2
885 neuromyelitis optica 10.2
886 allergic encephalomyelitis 10.2
887 lymphoma 10.2
888 monocular esotropia 10.2
889 hemosiderosis 10.2
890 leukemia 10.2
891 dermatitis 10.2
892 carotid artery disease 10.2
893 esotropia 10.2
894 olecranon bursitis 10.2 MRAP CRP
895 bursitis 10.2 MRAP CRP
896 chronic kidney disease 10.2
897 hypoglycemia 10.2
898 orbital plasma cell granuloma 10.2 MRAP CRP
899 deep keratitis 10.2 SAG MRAP
900 vitiligo-associated multiple autoimmune disease susceptibility 6 10.2
901 vitiligo-associated multiple autoimmune disease susceptibility 1 10.2
902 deficiency anemia 10.2
903 autosomal dominant cerebellar ataxia 10.2
904 leptospirosis 10.2
905 scotoma 10.2
906 refractive error 10.2
907 leukemia, acute lymphoblastic 10.2
908 end stage renal disease 10.2
909 first-degree atrioventricular block 10.2 CRP ACE
910 stroke, ischemic 10.2
911 myeloid leukemia 10.2
912 rare hereditary hemochromatosis 10.2
913 hypophosphatasia, childhood 10.2 MRAP ACE
914 discitis 10.2 MRAP CRP
915 mesenteric lymphadenitis 10.2 MRAP CRP
916 ankylosing spondylitis 3 10.2 MRAP CRP
917 blind hypotensive eye 10.2
918 carotid artery occlusion 10.2
919 pulmonary valve insufficiency 10.2 CRP ACE
920 constrictive pericarditis 10.2 CRP ACE
921 angioid streaks 10.2
922 corneal edema 10.2
923 myopathy 10.2
924 hypotonia 10.2
925 traumatic brain injury 10.2
926 balanitis 10.2 MRAP CRP
927 baastrup's syndrome 10.2 MRAP CRP
928 tuberous sclerosis 1 10.2
929 hydrocephalus 10.2
930 primary angle-closure glaucoma 10.2
931 schnitzler syndrome 10.2 CRP CD40LG
932 ocular dominance 10.2
933 incontinentia pigmenti 10.2
934 neutropenia 10.2
935 anisometropia 10.2
936 weber syndrome 10.2
937 polyradiculopathy 10.2 CRP CD40LG
938 nonarteritic anterior ischemic optic neuropathy 10.2
939 glaucoma, normal tension 10.2
940 joint laxity, short stature, and myopia 10.2
941 myopia 10.2
942 posterior uveitis 10.2
943 lymphadenitis 10.2
944 cauda equina syndrome 10.2 MRAP CRP
945 polykaryocytosis inducer 10.2
946 ocular motor apraxia 10.2
947 microvascular complications of diabetes 3 10.2
948 microvascular complications of diabetes 4 10.2
949 microvascular complications of diabetes 6 10.2
950 microvascular complications of diabetes 7 10.2
951 chondromalacia 10.1 MRAP CRP
952 thrombophilia due to activated protein c resistance 10.1
953 thrombotic thrombocytopenic purpura 10.1
954 anoxia 10.1
955 relapsing fever 10.1 CRP CD40LG
956 hypercarotenemia and vitamin a deficiency, autosomal dominant 10.1
957 optic nerve hypoplasia, bilateral 10.1
958 schizophrenia 10.1
959 sturge-weber syndrome 10.1
960 triiodothyronine receptor auxiliary protein 10.1
961 keratoconus 10.1
962 keratomalacia 10.1
963 sympathetic ophthalmia 10.1
964 severe combined immunodeficiency 10.1
965 anemia, x-linked, with or without neutropenia and/or platelet abnormalities 10.1
966 hyperlipoproteinemia, type iii 10.1
967 alternating exotropia 10.1
968 exotropia 10.1
969 depression 10.1
970 tremor 10.1
971 nanophthalmos 10.1
972 allergic hypersensitivity disease 10.1
973 dementia 10.1
974 transient cerebral ischemia 10.1
975 rubella 10.1
976 pik3ca-related overgrowth syndrome 10.1
977 optic disc pit 10.1
978 coronary artery vasospasm 10.1 CRP ACE
979 periostitis 10.1 MRAP CRP
980 left bundle branch hemiblock 10.1 CRP ACE
981 central sleep apnea 10.1 CRP ACE
982 malaria 10.1
983 severe pre-eclampsia 10.1
984 adenocarcinoma 10.1
985 immune deficiency disease 10.1
986 retinal vein occlusion 10.1
987 macular holes 10.1
988 retinal degeneration 10.1
989 diabetic macular edema 10.1
990 hypereosinophilic syndrome 10.1
991 angiomatosis 10.1
992 amyotrophic lateral sclerosis 1 10.1
993 fibrosis of extraocular muscles, congenital, 1 10.1
994 galactosemia i 10.1
995 coronary heart disease 1 10.1
996 thrombocytopenia 10.1
997 lateral sclerosis 10.1
998 iron metabolism disease 10.1
999 hemoglobinopathy 10.1
1000 teratoma 10.1
1001 polycythemia 10.1
1002 chronic pyelonephritis 10.1 CRP ACE
1003 amaurosis congenita, cone-rod type, with congenital hypertrichosis 10.1
1004 fleck retina of kandori 10.1
1005 atypical norrie disease due to xp11.3 microdeletion 10.1
1006 multifocal pattern dystrophy simulating fundus flavimaculatus 10.1
1007 acute closed-angle glaucoma 10.1
1008 protein s deficiency 10.1
1009 crohn's disease 10.1
1010 japanese spotted fever 10.1 CS CRP CD40LG
1011 subacute sclerosing panencephalitis 10.1
1012 cycloplegia 10.1
1013 cardiac tamponade 10.1 CRP ACE
1014 cork-handlers' disease 10.1 CD40LG CD4
1015 apnea, obstructive sleep 10.1
1016 exfoliation syndrome 10.1
1017 proteasome-associated autoinflammatory syndrome 1 10.1
1018 major affective disorder 8 10.1
1019 major affective disorder 9 10.1
1020 alacrima, achalasia, and mental retardation syndrome 10.1
1021 churg-strauss syndrome 10.1
1022 bipolar disorder 10.1
1023 wyburn-mason syndrome 10.1
1024 american histoplasmosis 10.1 CD40LG CD4
1025 syphilitic meningitis 10.1 CD40LG CD4
1026 early yaws 10.1 CD40LG CD4
1027 mucopolysaccharidosis-plus syndrome 10.1
1028 aniseikonia 10.1
1029 malignant choroid melanoma 10.1
1030 diabetic neuropathy 10.1
1031 allergic angiitis 10.1
1032 wallerian degeneration 10.1
1033 brain injury 10.1
1034 gastroduodenitis 10.1 CD40LG CD4
1035 primary syphilis 10.1 CD40LG CD4
1036 norwegian scabies 10.1 CD40LG CD4
1037 necrotizing ulcerative gingivitis 10.1 CD40LG CD4
1038 tertiary neurosyphilis 10.1 CD40LG CD4
1039 muscular dystrophy, duchenne type 10.1
1040 polydactyly 10.1
1041 lysosomal storage disease 10.1
1042 farsightedness 10.1
1043 cerebral lymphoma 10.0 CD40LG CD4
1044 exanthema subitum 10.0 CD40LG CD4
1045 neurofibromatosis, type ii 10.0
1046 huntington disease 10.0
1047 birdshot chorioretinopathy 10.0
1048 siderosis 10.0
1049 vitreous syneresis 10.0
1050 nephrotic syndrome 10.0
1051 hellp syndrome 10.0
1052 homocystinuria 10.0
1053 multiple sclerosis 10.0
1054 macular degeneration, age-related, 1 10.0
1055 tubulointerstitial nephritis with uveitis 10.0
1056 chikungunya 10.0
1057 mumps 10.0
1058 aseptic meningitis 10.0
1059 branch retinal artery occlusion 10.0
1060 central retinal vein occlusion 10.0
1061 antiphospholipid syndrome 10.0
1062 retinal artery occlusion 10.0
1063 diabetes mellitus 10.0
1064 meningitis 10.0
1065 ischemic colitis 10.0 CRP ACE
1066 west nile encephalitis 10.0 CD40LG CD4
1067 anuria 10.0 CRP CD40LG ACE
1068 autoimmune peripheral neuropathy 10.0 CD40LG CD4
1069 pyelitis 10.0 CRP CD40LG ACE
1070 trichinosis 10.0 CD40LG CD4
1071 hypersensitivity reaction type iii disease 10.0 CRP CD40LG ACE
1072 aspiration pneumonia 10.0 CRP CD40LG ACE
1073 marfan syndrome 10.0
1074 fryns microphthalmia syndrome 10.0
1075 sickle cell anemia 10.0
1076 bainbridge-ropers syndrome 10.0
1077 pulmonary hypertension 10.0
1078 thalassemia 10.0
1079 amyloidosis 10.0
1080 alopecia 10.0
1081 ndp-related retinopathies 10.0
1082 ring chromosome 2 10.0
1083 overgrowth syndrome 10.0
1084 mycoplasma pneumoniae pneumonia 10.0 CRP CD40LG ACE
1085 chancroid 10.0 CD40LG CD4
1086 pulmonary artery disease 10.0 CRP CD40LG ACE
1087 abnormal threshold of rods 10.0 TRPM1 SAG
1088 limited scleroderma 10.0 CRP CD40LG ACE
1089 west nile fever 10.0 CD40LG CD4
1090 splenic sequestration 10.0 CD40LG CD4
1091 chronic orbital inflammation 10.0 MRAP CRP CD40LG
1092 aniridia 1 10.0
1093 smith-lemli-opitz syndrome 10.0
1094 west syndrome 10.0
1095 ocular albinism 10.0
1096 iron deficiency anemia 10.0
1097 acute leukemia 10.0
1098 hypothyroidism 10.0
1099 hypogonadism 10.0
1100 thrombocytosis 10.0
1101 congestive heart failure 10.0
1102 neuroblastoma 10.0
1103 seizure disorder 10.0
1104 acute macular neuroretinopathy 10.0
1105 argyria 10.0
1106 paralytic poliomyelitis 10.0 CD40LG CD4
1107 tenosynovitis 10.0 MRAP CRP CD40LG
1108 blastomycosis 10.0 CD40LG CD4
1109 tendinitis 10.0 MRAP CRP CD40LG
1110 autoimmune neuropathy 10.0 CD40LG CD4
1111 hypertriglyceridemia, familial 10.0
1112 posterior column ataxia 10.0
1113 leukemia, acute myeloid 10.0
1114 major depressive disorder 10.0
1115 inflammatory bowel disease 10.0
1116 infective endocarditis 10.0
1117 diphtheria 10.0
1118 impotence 10.0
1119 pituitary adenoma 10.0
1120 congenital nystagmus 10.0
1121 mitochondrial disorders 10.0
1122 chromosomal triplication 10.0
1123 adenoid hypertrophy 10.0 CD40LG CD4
1124 tricuspid valve insufficiency 10.0 CRP ACE
1125 mite infestation 10.0 CD40LG CD4
1126 monkeypox 10.0 CD40LG CD4
1127 down syndrome 10.0
1128 arterial tortuosity syndrome 10.0
1129 chorea, childhood-onset, with psychomotor retardation 10.0
1130 secondary progressive multiple sclerosis 10.0
1131 migraine with aura 10.0
1132 alport syndrome 10.0
1133 choreatic disease 10.0
1134 gaucher's disease 10.0
1135 hyperinsulinism 10.0
1136 color vision deficiency 10.0
1137 skin sarcoidosis 10.0 CD4 ACE
1138 taeniasis 10.0 CD40LG CD4
1139 immunodeficiency with hyper-igm, type 3 10.0 CD40LG CD4
1140 glaucoma-related pigment dispersion syndrome 10.0
1141 autoimmune optic neuritis 10.0
1142 atrial fibrillation 10.0
1143 polycystic kidney disease 10.0
1144 orbital cellulitis 10.0
1145 gestational diabetes 10.0
1146 leukocoria 10.0
1147 epilepsy 10.0
1148 essential thrombocythemia 10.0
1149 acromegaly 10.0
1150 macroglobulinemia 10.0
1151 dwarfism 10.0
1152 trichomoniasis 10.0 CD40LG CD4
1153 optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy 10.0
1154 rheumatoid arthritis 10.0
1155 scleroderma, familial progressive 10.0
1156 familial mediterranean fever 10.0
1157 leukemia, acute lymphoblastic 3 10.0
1158 lens subluxation 10.0
1159 autonomic neuropathy 10.0
1160 visual epilepsy 10.0
1161 chronic progressive external ophthalmoplegia 10.0
1162 heart septal defect 10.0
1163 dyskeratosis congenita 10.0
1164 senile cataract 10.0
1165 myotonic dystrophy 10.0
1166 fungal meningitis 10.0 CD40LG CD4
1167 exudative vitreoretinopathy 1 10.0
1168 hemifacial atrophy, progressive 10.0
1169 keratitis, hereditary 10.0
1170 pheochromocytoma 10.0
1171 thrombophilia due to thrombin defect 10.0
1172 volvulus of midgut 10.0
1173 adrenoleukodystrophy 10.0
1174 microvascular complications of diabetes 1 10.0
1175 body mass index quantitative trait locus 1 10.0
1176 alpha/beta t-cell lymphopenia with gamma/delta t-cell expansion, severe cytomegalovirus infection, and autoimmunity 10.0
1177 microvascular complications of diabetes 2 10.0
1178 adrenal gland pheochromocytoma 10.0
1179 microphthalmia 10.0
1180 malignant hypertension 10.0
1181 sarcoma 10.0
1182 chlamydia 10.0
1183 color blindness 10.0
1184 neovascular glaucoma 10.0
1185 facial hemiatrophy 10.0
1186 hepatitis c 10.0
1187 spindle cell sarcoma 10.0
1188 retinal disease 10.0
1189 conjunctivitis 10.0
1190 herpes simplex 10.0
1191 lupus erythematosus 10.0
1192 adrenomyeloneuropathy 10.0
1193 herpes zoster ophthalmicus 10.0
1194 neurosyphilis 10.0
1195 ocular toxoplasmosis 10.0
1196 encephalopathy 10.0
1197 hypoxia 10.0
1198 tricuspid valve disease 10.0 CRP ACE
1199 degeneration of macula and posterior pole 9.9
1200 toxic maculopathy due to antimalarial drugs 9.9
1201 breast cancer 9.9
1202 gaucher disease, type i 9.9
1203 opitz gbbb syndrome, type i 9.9
1204 leukemia, chronic myeloid 9.9
1205 small cell carcinoma 9.9
1206 pain agnosia 9.9
1207 scrapie 9.9
1208 psoriasis 9.9
1209 stomatitis 9.9
1210 neonatal herpes 9.9
1211 cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1 9.9
1212 renal cell carcinoma, nonpapillary 9.9
1213 meningioma, radiation-induced 9.9
1214 pulmonary disease, chronic obstructive 9.9
1215 meningioma, familial 9.9
1216 graft-versus-host disease 9.9
1217 primary congenital glaucoma 9.9
1218 spastic ataxia 9.9
1219 spinal meningioma 9.9
1220 scleral staphyloma 9.9
1221 inflammatory spondylopathy 9.9
1222 mature cataract 9.9
1223 chronic closed-angle glaucoma 9.9
1224 candidiasis 9.9
1225 mental depression 9.9
1226 sensory peripheral neuropathy 9.9
1227 secretory meningioma 9.9
1228 lymphoplasmacyte-rich meningioma 9.9
1229 bilateral retinoblastoma 9.9
1230 paraplegia 9.9
1231 lymphopenia 9.9
1232 spondylitis 9.9
1233 t-cell lymphoblastic leukemia/lymphoma 9.9
1234 nervous system disease 9.9
1235 acute mountain sickness 9.9
1236 leukemia, t-cell, chronic 9.9
1237 cerebrofacial arteriovenous metameric syndrome 9.9
1238 intestinal tuberculosis 9.9 CRP CD4
1239 autoimmune disease of urogenital tract 9.9 CD40LG CD4
1240 colorectal cancer 9.9
1241 multiple system atrophy 1 9.9
1242 familial adenomatous polyposis 1 9.9
1243 fabry disease 9.9
1244 orthostatic intolerance 9.9
1245 hypertension, early-onset, autosomal dominant, with severe exacerbation in pregnancy 9.9
1246 myocardial infarction 9.9
1247 peripheral vascular disease 9.9
1248 oculocutaneous albinism 9.9
1249 primary progressive multiple sclerosis 9.9
1250 leukodystrophy 9.9
1251 glucose intolerance 9.9
1252 corneal neovascularization 9.9
1253 hemolytic-uremic syndrome 9.9
1254 hyperuricemia 9.9
1255 central nervous system lymphoma 9.9
1256 chronic granulomatous disease 9.9
1257 central nervous system disease 9.9
1258 liver disease 9.9
1259 mutism 9.9
1260 primary ciliary dyskinesia 9.9
1261 x-linked congenital stationary night blindness 9.9
1262 congenital cytomegalovirus 9.9
1263 hypertonia 9.9
1264 lassa fever 9.9 CD40LG CD4
1265 rheumatoid arthritis interstitial lung disease 9.9 CRP CD4
1266 pericardial tuberculosis 9.9 CRP CD4
1267 corneal dystrophy, band-shaped 9.9
1268 hemochromatosis, type 1 9.9
1269 laryngoonychocutaneous syndrome 9.9
1270 asplenia, isolated congenital 9.9
1271 aplastic anemia 9.9
1272 pulmonary fibrosis and/or bone marrow failure, telomere-related, 2 9.9
1273 brachydactyly 9.9
1274 hereditary ataxia 9.9
1275 hemiplegia 9.9
1276 absolute glaucoma 9.9
1277 ichthyosis 9.9
1278 squamous cell carcinoma 9.9
1279 acute kidney failure 9.9
1280 mood disorder 9.9
1281 lactic acidosis 9.9
1282 protein c deficiency 9.9
1283 hemolytic anemia 9.9
1284 lung disease 9.9
1285 hemophilia 9.9
1286 complete androgen insensitivity syndrome 9.9
1287 encephalocele 9.9
1288 growth hormone deficiency 9.9
1289 optic pathway glioma 9.9
1290 spasticity 9.9
1291 autosomal recessive spastic ataxia 9.9
1292 juvenile nephronophthisis 9.9
1293 pyomyositis 9.9 CRP CD4
1294 intestinal schistosomiasis 9.9 CD40LG CD4
1295 breast abscess 9.9 CRP CD4
1296 acute orbital inflammation 9.9 CRP CD4
1297 arachnoiditis 9.9 CRP CD4
1298 acute interstitial pneumonia 9.9 CRP CD4
1299 diabetes mellitus, noninsulin-dependent 9.9
1300 pulmonary hypertension, primary, 1 9.9
1301 cystic fibrosis 9.9
1302 myasthenia gravis 9.9
1303 brittle bone disorder 9.9
1304 lung cancer susceptibility 3 9.9
1305 cyanosis, transient neonatal 9.9
1306 diffuse large b-cell lymphoma 9.9
1307 cerebellar hypoplasia 9.9
1308 cerebral artery occlusion 9.9
1309 presbyopia 9.9
1310 common variable immunodeficiency 9.9
1311 migraine without aura 9.9
1312 atrial heart septal defect 9.9
1313 membranoproliferative glomerulonephritis 9.9
1314 early myoclonic encephalopathy 9.9
1315 orofaciodigital syndrome 9.9
1316 unilateral retinoblastoma 9.9
1317 brain edema 9.9
1318 dystonia 9.9
1319 t-cell acute lymphoblastic leukemia 9.9
1320 viral encephalitis 9.9
1321 mitochondrial metabolism disease 9.9
1322 influenza 9.9
1323 carotid artery dissection 9.9
1324 alopecia areata 9.9
1325 mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes 9.9
1326 ornithinemia 9.9
1327 ring chromosome 3 9.9
1328 cerebral arteriosclerosis 9.9
1329 cerebral visual impairment 9.9
1330 methanol poisoning 9.9
1331 premature aging 9.9
1332 primary thrombocytopenia 9.9 CD40LG CD4
1333 oral tuberculosis 9.8 CRP CD4
1334 tularemia 9.8 CD40LG CD4
1335 atrial standstill 1 9.8
1336 blood group--newfoundland 9.8
1337 attention deficit-hyperactivity disorder 9.8
1338 takayasu arteritis 9.8
1339 leukoencephalopathy, hereditary diffuse, with spheroids 9.8
1340 lymphoma, hodgkin, classic 9.8
1341 thymoma, familial 9.8
1342 mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes 9.8
1343 muscular dystrophy, congenital, lmna-related 9.8
1344 myelodysplastic syndrome 9.8
1345 mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome 9.8
1346 lissencephaly 9.8
1347 adult t-cell leukemia 9.8
1348 metabolic acidosis 9.8
1349 peripheral artery disease 9.8
1350 scoliosis 9.8
1351 paroxysmal nocturnal hemoglobinuria 9.8
1352 anterior segment dysgenesis 9.8
1353 mucolipidosis 9.8
1354 corneal disease 9.8
1355 dermatomyositis 9.8
1356 ametropic amblyopia 9.8
1357 juvenile glaucoma 9.8
1358 renal hypertension 9.8
1359 spotted fever 9.8
1360 rabies 9.8
1361 diarrhea 9.8
1362 rift valley fever 9.8
1363 toxic optic neuropathy 9.8
1364 methylmalonic acidemia 9.8
1365 agammaglobulinemia 9.8
1366 thymoma 9.8
1367 mixed connective tissue disease 9.8
1368 thrombophlebitis 9.8
1369 optic nerve glioma 9.8
1370 arteriolosclerosis 9.8
1371 human immunodeficiency virus infectious disease 9.8
1372 hemoglobinuria 9.8
1373 ocular hypotension 9.8
1374 vascular dementia 9.8
1375 keratoconjunctivitis 9.8
1376 diabetes insipidus 9.8
1377 fatty liver disease 9.8
1378 neurofibroma 9.8
1379 serpiginous choroiditis 9.8
1380 transverse myelitis 9.8
1381 raynaud phenomenon 9.8
1382 myoclonus 9.8
1383 paraneoplastic syndromes 9.8
1384 whiplash 9.8
1385 isolated optic neuritis 9.8
1386 thrombotic microangiopathy 9.8
1387 kwashiorkor 9.8 CRP CD4
1388 granulomatous dermatitis 9.8 CD40LG CD4 ACE
1389 autoimmune vasculitis 9.8 CRP CD4
1390 pfeiffer syndrome 9.8
1391 coarctation of aorta 9.8
1392 coloboma of macula 9.8
1393 kaposi sarcoma 9.8
1394 systemic lupus erythematosus 9.8
1395 parkinson disease, late-onset 9.8
1396 dowling-degos disease 1 9.8
1397 tritanopia 9.8
1398 ceroid lipofuscinosis, neuronal, 3 9.8
1399 ceroid storage disease 9.8
1400 multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly 9.8
1401 myeloma, multiple 9.8
1402 coats disease 9.8
1403 astigmatism 9.8
1404 homocysteinemia 9.8
1405 human immunodeficiency virus type 1 9.8
1406 hepatitis c virus 9.8
1407 complement factor h deficiency 9.8
1408 west nile virus 9.8
1409 retinitis pigmentosa 4 9.8
1410 neuronal ceroid-lipofuscinoses 9.8
1411 arteritic anterior ischemic optic neuropathy 9.8
1412 colitis 9.8
1413 ptosis 9.8
1414 thrombosis 9.8
1415 renal hypoplasia 9.8
1416 endocarditis 9.8
1417 suppression amblyopia 9.8
1418 amblyopia 9.8
1419 tonsillitis 9.8
1420 pre-eclampsia 9.8
1421 brucellosis 9.8
1422 chorioretinal scar 9.8
1423 enophthalmos 9.8
1424 retinal microaneurysm 9.8
1425 tetanus 9.8
1426 autonomic nervous system disease 9.8
1427 onchocerciasis 9.8
1428 pica disease 9.8
1429 dengue disease 9.8
1430 telangiectasis 9.8
1431 intermediate uveitis 9.8
1432 optic disk drusen 9.8
1433 acute retrobulbar neuritis 9.8
1434 neuronal ceroid lipofuscinosis 9.8
1435 retinal vascular occlusion 9.8
1436 histoplasmosis 9.8
1437 viral hepatitis 9.8
1438 melanoma 9.8
1439 glomerulonephritis 9.8
1440 lipid metabolism disorder 9.8
1441 demyelinating disease 9.8
1442 ischemia 9.8
1443 sleep disorder 9.8
1444 placenta disease 9.8
1445 cataract 9.8
1446 chronic fatigue syndrome 9.8
1447 ulcerative colitis 9.8
1448 measles 9.8
1449 metagonimiasis 9.8
1450 skin melanoma 9.8
1451 peliosis hepatis 9.8
1452 intracranial hypertension 9.8
1453 encephalitis 9.8
1454 polyarteritis nodosa 9.8
1455 47,xyy 9.8
1456 anca-associated vasculitis 9.8
1457 baylisascaris infection 9.8
1458 central serous chorioretinopathy 9.8
1459 distomatosis 9.8
1460 herpes simplex encephalitis 9.8
1461 multifocal choroiditis 9.8
1462 punctate inner choroidopathy 9.8
1463 splenomegaly 9.8
1464 autonomic dysfunction 9.8
1465 cerebral atrophy 9.8
1466 cytomegalovirus infection 9.8
1467 headache 9.8
1468 pituitary tumors 9.8
1469 rapidly involuting congenital hemangioma 9.8
1470 transient pseudohypoaldosteronism 9.8
1471 transient arthritis 9.8 MRAP CD40LG CD4
1472 cleft palate, isolated 9.8
1473 creutzfeldt-jakob disease 9.8
1474 esophageal cancer 9.8
1475 fibromuscular dysplasia 9.8
1476 hypertelorism 9.8
1477 progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 1 9.8
1478 osteoporosis 9.8
1479 ataxia-telangiectasia 9.8
1480 chediak-higashi syndrome 9.8
1481 intracranial hypertension, idiopathic 9.8
1482 polycythemia vera 9.8
1483 reticulum cell sarcoma 9.8
1484 body mass index quantitative trait locus 11 9.8
1485 orofaciodigital syndrome i 9.8
1486 lymphoma, non-hodgkin, familial 9.8
1487 long-chain 3-hydroxyacyl-coa dehydrogenase deficiency 9.8
1488 progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 2 9.8
1489 progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 4 9.8
1490 bone mineral density quantitative trait locus 8 9.8
1491 congenital disorder of glycosylation, type in 9.8
1492 diabetes mellitus, ketosis-prone 9.8
1493 bone mineral density quantitative trait locus 15 9.8
1494 aspergillosis 9.8
1495 dengue virus 9.8
1496 hydrops, lactic acidosis, and sideroblastic anemia 9.8
1497 hemophagocytic lymphohistiocytosis 9.8
1498 autism spectrum disorder 9.8
1499 non-alcoholic fatty liver disease 9.8
1500 charcot-marie-tooth disease 9.8
1501 filariasis 9.8
1502 disseminated intravascular coagulation 9.8
1503 nephrocalcinosis 9.8
1504 hereditary hemorrhagic telangiectasia 9.8
1505 olivopontocerebellar atrophy 9.8
1506 ectodermal dysplasia 9.8
1507 corneal dystrophy 9.8
1508 glucosephosphate dehydrogenase deficiency 9.8
1509 acute pancreatitis 9.8
1510 cryoglobulinemia 9.8
1511 cystic kidney disease 9.8
1512 iga glomerulonephritis 9.8
1513 heart valve disease 9.8
1514 pancreatitis 9.8
1515 infertility 9.8
1516 pneumonia 9.8
1517 prion disease 9.8
1518 juvenile rheumatoid arthritis 9.8
1519 mitochondrial myopathy 9.8
1520 situs inversus 9.8
1521 learning disability 9.8
1522 autosomal dominant polycystic kidney disease 9.8
1523 cataract-glaucoma 9.8
1524 charles bonnet syndrome 9.8
1525 primary central nervous system lymphoma 9.8
1526 early-onset glaucoma 9.8
1527 cerebral aneurysms 9.8
1528 mucopolysaccharidoses 9.8
1529 rare tumor 9.8
1530 alcohol dependence 9.8
1531 machado-joseph disease 9.8
1532 bladder cancer 9.8
1533 cerebral cavernous malformations 9.8
1534 hair whorl 9.8
1535 myositis 9.8
1536 neurofibromatosis, type i 9.8
1537 ovarian cancer 9.8
1538 schistosoma mansoni infection, susceptibility/ 9.8
1539 sneddon syndrome 9.8
1540 neural tube defects 9.8
1541 short-rib thoracic dysplasia 1 with or without polydactyly 9.8
1542 factor xii deficiency 9.8
1543 mckusick-kaufman syndrome 9.8
1544 hypoascorbemia 9.8
1545 moyamoya disease 1 9.8
1546 leigh syndrome 9.8
1547 danon disease 9.8
1548 frontotemporal dementia 9.8
1549 nephronophthisis 4 9.8
1550 nasopharyngeal carcinoma 9.8
1551 anxiety 9.8
1552 muscle hypertrophy 9.8
1553 leptin deficiency or dysfunction 9.8
1554 lymphoplasmacytic lymphoma 9.8
1555 paraganglioma 9.8
1556 crohn's colitis 9.8
1557 covid-19 9.8
1558 rickets 9.8
1559 wolfram syndrome 9.8
1560 pulmonary edema 9.8
1561 cortical blindness 9.8
1562 gout 9.8
1563 typhoid fever 9.8
1564 megaloblastic anemia 9.8
1565 visual pathway disease 9.8
1566 schistosomiasis 9.8
1567 vitreoretinal dystrophy 9.8
1568 gonadal dysgenesis 9.8
1569 ventricular septal defect 9.8
1570 neuroma 9.8
1571 craniosynostosis 9.8
1572 primary hyperoxaluria 9.8
1573 turner syndrome 9.8
1574 cavernous sinus thrombosis 9.8
1575 craniopharyngioma 9.8
1576 holoprosencephaly 9.8
1577 intraocular retinoblastoma 9.8
1578 borna disease 9.8
1579 bronchitis 9.8
1580 juvenile pilocytic astrocytoma 9.8
1581 compartment syndrome 9.8
1582 arthritis 9.8
1583 collagen disease 9.8
1584 hypopituitarism 9.8
1585 acute myocardial infarction 9.8
1586 bronchiectasis 9.8
1587 hypertropia 9.8
1588 vcan-related vitreoretinopathy 9.8
1589 bronchopulmonary dysplasia 9.8
1590 chronic graft versus host disease 9.8
1591 coloboma of iris 9.8
1592 granulocytopenia 9.8
1593 light chain deposition disease 9.8
1594 microscopic polyangiitis 9.8
1595 muscle eye brain disease 9.8
1596 ring chromosome 5 9.8
1597 spastic paraparesis 9.8
1598 endotheliitis 9.8
1599 infectious posterior uveitis 9.8
1600 juvenile nasopharyngeal angiofibroma 9.8
1601 benign idiopathic neonatal seizures 9.8
1602 peripapillary staphyloma 9.8
1603 laminopathy 9.8
1604 autoimmune disease of peripheral nervous system 9.7 DPYSL5 CD40LG CD4
1605 thymus gland disease 9.7 DPYSL5 CD40LG CD4
1606 thymus cancer 9.7 DPYSL5 CD40LG CD4
1607 intestinal perforation 9.7 CRP CD4
1608 meningovascular neurosyphilis 9.7 CRP CD40LG CD4
1609 viral exanthem 9.7 CRP CD40LG CD4
1610 tertiary syphilis 9.7 CRP CD40LG CD4
1611 opportunistic bacterial infectious disease 9.7 CRP CD40LG CD4
1612 gastrointestinal tuberculosis 9.7 CRP CD40LG CD4
1613 granulomatous hepatitis 9.7 CRP CD40LG CD4
1614 mikulicz disease 9.7 CRP CD40LG CD4
1615 mononeuritis of upper limb and mononeuritis multiplex 9.7 CRP CD40LG CD4
1616 parotid disease 9.7 CRP CD40LG CD4
1617 cervical adenitis 9.7 CRP CD40LG CD4
1618 lung abscess 9.7 CRP CD40LG CD4
1619 aortic valve disease 1 9.7
1620 cardiac arrhythmia 9.7
1621 spondyloepiphyseal dysplasia with congenital joint dislocations 9.7
1622 leukemia, chronic lymphocytic 9.7
1623 hutchinson-gilford progeria syndrome 9.7
1624 septooptic dysplasia 9.7
1625 tetralogy of fallot 9.7
1626 varicose veins 9.7
1627 autism 9.7
1628 cryptorchidism, unilateral or bilateral 9.7
1629 3-hydroxyacyl-coa dehydrogenase deficiency 9.7
1630 hallermann-streiff syndrome 9.7
1631 mucopolysaccharidosis, type vii 9.7
1632 myelofibrosis 9.7
1633 myoclonic epilepsy of unverricht and lundborg 9.7
1634 peters-plus syndrome 9.7
1635 prepapillary vascular loops 9.7
1636 sudden infant death syndrome 9.7
1637 vitamin e, familial isolated deficiency of 9.7
1638 wilson disease 9.7
1639 tubulin, beta 9.7
1640 hemophilia a 9.7
1641 congenital hemidysplasia with ichthyosiform erythroderma and limb defects 9.7
1642 supranuclear palsy, progressive, 1 9.7
1643 body mass index quantitative trait locus 9 9.7
1644 body mass index quantitative trait locus 8 9.7
1645 diamond-blackfan anemia 2 9.7
1646 atrioventricular septal defect 9.7
1647 patent ductus arteriosus 1 9.7
1648 body mass index quantitative trait locus 4 9.7
1649 body mass index quantitative trait locus 10 9.7
1650 body mass index quantitative trait locus 7 9.7
1651 myopia 6 9.7
1652 body mass index quantitative trait locus 12 9.7
1653 body mass index quantitative trait locus 14 9.7
1654 body mass index quantitative trait locus 18 9.7
1655 body mass index quantitative trait locus 19 9.7
1656 body mass index quantitative trait locus 20 9.7
1657 juvenile arthritis 9.7
1658 fetal alcohol syndrome 9.7
1659 alcohol-related birth defect 9.7
1660 ameloblastoma 9.7
1661 cardiac arrest 9.7
1662 waldenstroem's macroglobulinemia 9.7
1663 blepharophimosis 9.7
1664 protein-losing enteropathy 9.7
1665 cystinosis 9.7
1666 tooth disease 9.7
1667 intracranial aneurysm 9.7
1668 polycystic ovary syndrome 9.7
1669 diabetic angiopathy 9.7
1670 ischemic neuropathy 9.7
1671 lymphocytic choriomeningitis 9.7
1672 graves' disease 9.7
1673 acoustic neuroma 9.7
1674 mucopolysaccharidosis iii 9.7
1675 hereditary spherocytosis 9.7
1676 poems syndrome 9.7
1677 toxic shock syndrome 9.7
1678 alcohol use disorder 9.7
1679 mitral valve stenosis 9.7
1680 cerebral palsy 9.7
1681 hepatitis b 9.7
1682 myeloproliferative neoplasm 9.7
1683 acquired polycythemia 9.7
1684 hairy cell leukemia 9.7
1685 hemoglobin c disease 9.7
1686 interstitial lung disease 9.7
1687 neurilemmoma 9.7
1688 histiocytosis 9.7
1689 aortic aneurysm 9.7
1690 skin disease 9.7
1691 plasmacytoma 9.7
1692 hermansky-pudlak syndrome 9.7
1693 pulmonary fibrosis 9.7
1694 placental insufficiency 9.7
1695 neuromuscular disease 9.7
1696 hypotrichosis 9.7
1697 medulloepithelioma 9.7
1698 muscular atrophy 9.7
1699 hyperthyroidism 9.7
1700 cocaine abuse 9.7
1701 mitochondrial encephalomyopathy 9.7
1702 cleft lip 9.7
1703 blepharitis 9.7
1704 dacryoadenitis 9.7
1705 placental abruption 9.7
1706 accommodative esotropia 9.7
1707 c3 glomerulopathy 9.7
1708 catastrophic antiphospholipid syndrome 9.7
1709 cerebellar degeneration 9.7
1710 congenital hepatic fibrosis 9.7
1711 dense deposit disease 9.7
1712 methylmalonic acidemia with homocystinuria 9.7
1713 pediatric multiple sclerosis 9.7
1714 ring chromosome 6 9.7
1715 west nile virus infection 9.7
1716 cavernous malformation 9.7
1717 dysautonomia 9.7
1718 paresthesia 9.7
1719 syncope 9.7
1720 phacoanaphylactic uveitis 9.7
1721 oligocone trichromacy 9.7
1722 salpingitis 9.7 CRP CD40LG CD4
1723 pleural empyema 9.7 CRP CD40LG CD4
1724 cryptogenic organizing pneumonia 9.7 CRP CD40LG CD4
1725 vaginal discharge 9.7 CRP CD40LG CD4
1726 acute proliferative glomerulonephritis 9.7 CRP CD40LG CD4
1727 viral pneumonia 9.7 CRP CD40LG CD4
1728 urinary system disease 9.7 CRP CD40LG ACE
1729 primary systemic mycosis 9.7 CRP CD40LG CD4
1730 cecal disease 9.7 CRP CD40LG CD4
1731 bronchopneumonia 9.7 CRP CD40LG CD4
1732 streptococcus pneumonia 9.7 CRP CD40LG CD4
1733 fallopian tube disease 9.7 CRP CD40LG CD4
1734 plasma protein metabolism disease 9.7 CRP CD40LG CD4
1735 autoimmune disease of cardiovascular system 9.7 CRP CD40LG CD4
1736 autoimmune disease of blood 9.7 CRP CD40LG CD4
1737 pharyngitis 9.7 CRP CD40LG CD4
1738 autoimmune disease of exocrine system 9.7 CRP CD40LG CD4
1739 thrombocytopenia due to platelet alloimmunization 9.7 CD40LG CD4
1740 middle ear disease 9.7 CRP CD40LG CD4
1741 splenic disease 9.7 CRP CD40LG CD4
1742 paranasal sinus disease 9.7 CRP CD40LG CD4
1743 rectal disease 9.7 CRP CD40LG CD4
1744 opportunistic mycosis 9.7 CRP CD40LG CD4
1745 fungal infectious disease 9.7 CRP CD40LG CD4
1746 lymph node disease 9.7 CRP CD40LG CD4
1747 nose disease 9.7 CRP CD40LG CD4
1748 autoimmune disease of gastrointestinal tract 9.7 CRP CD40LG CD4
1749 commensal bacterial infectious disease 9.7 CRP CD40LG CD4
1750 pelvic inflammatory disease 9.7 CRP CD40LG CD4
1751 inclusion body myopathy with paget disease of bone and frontotemporal dementia 9.7 SAG CD40LG CD4
1752 lymphoid interstitial pneumonia 9.7 CRP CD40LG CD4
1753 potocki-shaffer syndrome 9.7 CRP CD40LG CD4
1754 blood platelet disease 9.7 CRP CD40LG CD4
1755 autoimmune disease of musculoskeletal system 9.7 CRP CD40LG CD4
1756 bronchial disease 9.7 CRP CD40LG CD4
1757 primary bacterial infectious disease 9.7 CRP CD40LG CD4
1758 inclusion body myopathy with early-onset paget disease of bone with or without frontotemporal dementia 2 9.7 SAG CS CD4
1759 bile duct disease 9.7 CRP CD40LG CD4
1760 autoimmune disease of eyes, ear, nose and throat 9.7 SAG RCVRN CD4
1761 immune-complex glomerulonephritis 9.6 CD40LG CD4
1762 achondroplasia 9.6
1763 cerebral amyloid angiopathy, cst3-related 9.6
1764 anisocoria 9.6
1765 burkitt lymphoma 9.6
1766 dentatorubral-pallidoluysian atrophy 9.6
1767 transient bullous dermolysis of the newborn 9.6
1768 hashimoto thyroiditis 9.6
1769 diaphragmatic hernia, congenital 9.6
1770 hypercalciuria, absorptive, 2 9.6
1771 ichthyosis vulgaris 9.6
1772 klippel-trenaunay-weber syndrome 9.6
1773 lacrimal duct defect 9.6
1774 medulloblastoma 9.6
1775 meniere disease 9.6
1776 noonan syndrome 1 9.6
1777 hemifacial microsomia 9.6
1778 split-hand/foot malformation 1 9.6
1779 chromosome 2q35 duplication syndrome 9.6
1780 thrombocytopenic purpura, autoimmune 9.6
1781 digeorge syndrome 9.6
1782 torticollis 9.6
1783 trichomegaly 9.6
1784 albinism, oculocutaneous, type ii 9.6
1785 lung cancer 9.6
1786 cutis marmorata telangiectatica congenita 9.6
1787 wolfram syndrome 1 9.6
1788 neuropathy, hereditary sensory and autonomic, type iii 9.6
1789 fanconi anemia, complementation group a 9.6
1790 hemolytic uremic syndrome, atypical 1 9.6
1791 leprosy 3 9.6
1792 meckel syndrome, type 1 9.6
1793 metachromatic leukodystrophy 9.6
1794 osteogenic sarcoma 9.6
1795 retinoschisis of fovea 9.6
1796 revesz syndrome 9.6
1797 sandhoff disease 9.6
1798 sjogren syndrome 9.6
1799 werner syndrome 9.6
1800 arts syndrome 9.6
1801 colorblindness, partial, deutan series 9.6
1802 hemophilia b 9.6
1803 menkes disease 9.6
1804 mucopolysaccharidosis, type ii 9.6
1805 androgen insensitivity, partial 9.6
1806 guanylate cyclase 2e, pseudogene 9.6
1807 nephronophthisis 2 9.6
1808 xanthomatosis 9.6
1809 alpha-thalassemia 9.6
1810 myopia 17, autosomal dominant 9.6
1811 platelet glycoprotein iv deficiency 9.6
1812 nanophthalmos 2 9.6
1813 acute promyelocytic leukemia 9.6
1814 membranous nephropathy 9.6
1815 gastrointestinal ulceration, recurrent, with dysfunctional platelets 9.6
1816 ophthalmomyiasis 9.6
1817 congenital hypothyroidism 9.6
1818 fetal alcohol spectrum disorder 9.6
1819 chorioamnionitis 9.6
1820 vitamin b12 deficiency 9.6
1821 peripheral t-cell lymphoma 9.6
1822 rheumatic heart disease 9.6
1823 limb ischemia 9.6
1824 apraxia 9.6
1825 zika fever 9.6
1826 isolated growth hormone deficiency 9.6
1827 bone disease 9.6
1828 middle east respiratory syndrome 9.6
1829 x-linked alport syndrome 9.6
1830 familial isolated trichomegaly 9.6
1831 brown's tendon sheath syndrome 9.6
1832 viral meningitis 9.6
1833 bullous keratopathy 9.6
1834 aqueous misdirection 9.6
1835 allergic conjunctivitis 9.6
1836 trachoma 9.6
1837 hemopericardium 9.6
1838 mitral valve insufficiency 9.6
1839 esophagitis 9.6
1840 hypertrophic cardiomyopathy 9.6
1841 chagas disease 9.6
1842 von willebrand's disease 9.6
1843 capillary disease 9.6
1844 ocular motility disease 9.6
1845 quadriplegia 9.6
1846 cardiovascular system disease 9.6
1847 keratoconjunctivitis sicca 9.6
1848 focal segmental glomerulosclerosis 9.6
1849 diabetic cataract 9.6
1850 ehlers-danlos syndrome 9.6
1851 osteopetrosis 9.6
1852 panophthalmitis 9.6
1853 irregular astigmatism 9.6
1854 amenorrhea 9.6
1855 childhood type dermatomyositis 9.6
1856 oral candidiasis 9.6
1857 corneal ectasia 9.6
1858 niemann-pick disease 9.6
1859 axenfeld-rieger syndrome 9.6
1860 disease of mental health 9.6
1861 constipation 9.6
1862 hemorrhagic disease 9.6
1863 hereditary spastic paraplegia 9.6
1864 relapsing polychondritis 9.6
1865 larynx cancer 9.6
1866 glycogen storage disease 9.6
1867 germinoma 9.6
1868 angiomyolipoma 9.6
1869 pyoderma 9.6
1870 dyslexia 9.6
1871 proliferative glomerulonephritis 9.6
1872 movement disease 9.6
1873 subependymal giant cell astrocytoma 9.6
1874 blepharospasm 9.6
1875 epulis 9.6
1876 eosinophilic pneumonia 9.6
1877 posterior uveal melanoma 9.6
1878 thyroiditis 9.6
1879 axonal neuropathy 9.6
1880 pineal region germinoma 9.6
1881 periodontitis 9.6
1882 subacute delirium 9.6
1883 genital herpes 9.6
1884 rosacea 9.6
1885 viral infectious disease 9.6
1886 bacterial meningitis 9.6
1887 yellow fever 9.6
1888 cyclotropia 9.6
1889 toxic maculopathy 9.6
1890 steroid-induced glaucoma 9.6
1891 nonsyndromic deafness 9.6
1892 zellweger spectrum disorder 9.6
1893 aminoaciduria 9.6
1894 cluster headache 9.6
1895 congenital muscular dystrophy due to dystroglycanopathy 9.6
1896 congenital rubella 9.6
1897 craniofacial microsomia 9.6
1898 dentinogenesis imperfecta type 2 9.6
1899 eisenmenger syndrome 9.6
1900 familial colorectal cancer 9.6
1901 gangliosidosis 9.6
1902 hansen's disease 9.6
1903 hereditary amyloidosis 9.6
1904 leukoplakia 9.6
1905 linear scleroderma 9.6
1906 macrophage activation syndrome 9.6
1907 mast cell activation syndrome 9.6
1908 polymyositis 9.6
1909 pseudo-turner syndrome 9.6
1910 rud syndrome 9.6
1911 tuberculous uveitis 9.6
1912 age-related hearing loss 9.6
1913 dysphagia 9.6
1914 spinal cord injury 9.6
1915 isolated split hand-split foot malformation 9.6
1916 specific language disorder 9.6
1917 acute sensory ataxic neuropathy 9.6
1918 qualitative or quantitative defects of alpha-dystroglycan 9.6
1919 non-infectious posterior uveitis 9.6
1920 glomerular disease 9.6
1921 atrial septal aneurysm 9.6
1922 intestinal polyposis syndrome 9.6
1923 rickettsial disease 9.6
1924 precursor t-cell acute lymphoblastic leukemia 9.6
1925 upper respiratory tract disease 9.6 CRP CD40LG CD4
1926 acute myocarditis 9.6 CRP CD4 ACE
1927 thyroid gland disease 9.6 CRP CD4 ACE
1928 blood group, globoside system 9.6 MRAP CRP CD4
1929 aortic aneurysm, familial abdominal, 1 9.6
1930 aplasia cutis congenita, nonsyndromic 9.6
1931 branchiooculofacial syndrome 9.6
1932 sotos syndrome 1 9.6
1933 alagille syndrome 1 9.6
1934 cryoglobulinemia, familial mixed 9.6
1935 duane retraction syndrome 1 9.6
1936 lymphoma, mucosa-associated lymphoid type 9.6
1937 hand skill, relative 9.6
1938 hernia, hiatus 9.6
1939 heterochromia iridis 9.6
1940 hirschsprung disease 1 9.6
1941 ige responsiveness, atopic 9.6
1942 myelinated optic nerve fibers 9.6
1943 myelopathy, htlv-1-associated 9.6
1944 myoclonus and ataxia 9.6
1945 obsessive-compulsive disorder 9.6
1946 pernicious anemia 9.6
1947 platelet membrane fluidity 9.6
1948 polycystic kidney disease 1 with or without polycystic liver disease 9.6
1949 proteus syndrome 9.6
1950 pulmonary fibrosis, idiopathic 9.6
1951 small cell cancer of the lung 9.6
1952 blau syndrome 9.6
1953 suppressor of tumorigenicity 3 9.6
1954 albinism, oculocutaneous, type ia 9.6
1955 ceroid lipofuscinosis, neuronal, 2 9.6
1956 anemia, autoimmune hemolytic 9.6
1957 buerger disease 9.6
1958 boucher-neuhauser syndrome 9.6
1959 achromatopsia 2 9.6
1960 central cloudy dystrophy of francois 9.6
1961 cystinuria 9.6
1962 mitochondrial complex iv deficiency 9.6
1963 schopf-schulz-passarge syndrome 9.6
1964 factor vii deficiency 9.6
1965 friedreich ataxia 9.6
1966 glaucoma 3, primary congenital, a 9.6
1967 mowat-wilson syndrome 9.6
1968 homocystinuria due to deficiency of n -methylenetetrahydrofolate reductase activity 9.6
1969 mannosidosis, alpha b, lysosomal 9.6
1970 megalocornea 9.6
1971 spondylometaphyseal dysplasia, sedaghatian type 9.6
1972 mitochondrial complex i deficiency, nuclear type 1 9.6
1973 myoclonic epilepsy of lafora 9.6
1974 hyperoxaluria, primary, type i 9.6
1975 hyper-igd syndrome 9.6
1976 d-bifunctional protein deficiency 9.6
1977 achromatopsia 3 9.6
1978 laron syndrome 9.6
1979 pulmonic stenosis 9.6
1980 glutathione synthetase deficiency 9.6
1981 ramon syndrome 9.6
1982 hemophagocytic lymphohistiocytosis, familial, 1 9.6
1983 muscular dystrophy, becker type 9.6
1984 fragile x syndrome 9.6
1985 mcleod syndrome 9.6
1986 aarskog-scott syndrome 9.6
1987 focal dermal hypoplasia 9.6
1988 mitochondrial complex v deficiency, mitochondrial type 1 9.6
1989 budd-chiari syndrome 9.6
1990 mitochondrial complex v deficiency, nuclear type 1 9.6
1991 nephronophthisis 3 9.6
1992 langerhans cell histiocytosis 9.6
1993 spinocerebellar ataxia 14 9.6
1994 hr44 antigen 9.6
1995 huntington disease-like 2 9.6
1996 lymphangioleiomyomatosis 9.6
1997 gastrointestinal stromal tumor 9.6
1998 anorexia nervosa 9.6
1999 bone mineral density quantitative trait locus 3 9.6
2000 deafness, autosomal recessive 31 9.6
2001 spastic paraplegia 7, autosomal recessive 9.6
2002 lissencephaly 1 9.6
2003 ovarian hyperstimulation syndrome 9.6
2004 kala-azar 1 9.6
2005 carney complex variant 9.6
2006 myopia 8 9.6
2007 myopia 10 9.6
2008 myopia 11, autosomal dominant 9.6
2009 myopia 14 9.6
2010 ceroid lipofuscinosis, neuronal, 7 9.6
2011 hemolytic anemia, cd59-mediated, with or without immune-mediated polyneuropathy 9.6
2012 myopia 15, autosomal dominant 9.6
2013 antithrombin iii deficiency 9.6
2014 fatty liver disease, nonalcoholic 1 9.6
2015 fanconi renotubular syndrome 2 9.6
2016 alpha-1-antitrypsin deficiency 9.6
2017 gastric cancer 9.6
2018 prothrombin deficiency, congenital 9.6
2019 short-rib thoracic dysplasia 4 with or without polydactyly 9.6
2020 beta-thalassemia 9.6
2021 ras-associated autoimmune leukoproliferative disorder 9.6
2022 cerebellar ataxia, neuropathy, and vestibular areflexia syndrome 9.6
2023 aortic valve disease 2 9.6
2024 hyperprolactinemia 9.6
2025 bardet-biedl syndrome 9 9.6
2026 patent ductus arteriosus 2 9.6
2027 spastic paraplegia, intellectual disability, nystagmus, and obesity 9.6
2028 alkuraya-kucinskas syndrome 9.6
2029 polymicrogyria with or without vascular-type ehlers-danlos syndrome 9.6
2030 angina pectoris 9.6
2031 sydenham chorea 9.6
2032 erythema multiforme 9.6
2033 weill-marchesani syndrome 9.6
2034 hereditary sensory neuropathy 9.6
2035 tooth agenesis 9.6
2036 aicardi-goutieres syndrome 9.6
2037 spastic cerebral palsy 9.6
2038 renal fibrosis 9.6
2039 pervasive developmental disorder 9.6
2040 aphasia 9.6
2041 brain meningioma 9.6
2042 cogan syndrome 9.6
2043 crest syndrome 9.6
2044 cold-induced sweating syndrome 9.6
2045 autosomal recessive non-syndromic intellectual disability 9.6
2046 myelomeningocele 9.6
2047 lymphoproliferative syndrome 9.6
2048 hereditary lymphedema i 9.6
2049 primary autosomal recessive microcephaly 9.6
2050 primary microcephaly 9.6
2051 childhood acute myeloid leukemia 9.6
2052 x-linked recessive disease 9.6
2053 childhood acute lymphocytic leukemia 9.6
2054 peroxisomal biogenesis disorder 9.6
2055 aortic dissection 9.6
2056 hypogonadotropic hypogonadism 9.6
2057 castleman disease 9.6
2058 osteomyelitis 9.6
2059 cholelithiasis 9.6
2060 pleurisy 9.6
2061 chronic leukemia 9.6
2062 prolymphocytic leukemia 9.6
2063 fanconi syndrome 9.6
2064 primary optic atrophy 9.6
2065 japanese encephalitis 9.6
2066 hand, foot and mouth disease 9.6
2067 amnestic disorder 9.6
2068 hydronephrosis 9.6
2069 hypoparathyroidism 9.6
2070 esophageal varix 9.6
2071 primary hyperparathyroidism 9.6
2072 pyelonephritis 9.6
2073 hypertensive heart disease 9.6
2074 nephrosclerosis 9.6
2075 prediabetes syndrome 9.6
2076 synostosis 9.6
2077 bullous retinoschisis 9.6
2078 goiter 9.6
2079 corneal degeneration 9.6
2080 spinal muscular atrophy 9.6
2081 hepatitis a 9.6
2082 duane retraction syndrome 9.6
2083 phacolytic glaucoma 9.6
2084 dilated cardiomyopathy 9.6
2085 plasmodium vivax malaria 9.6
2086 subclavian steal syndrome 9.6
2087 traumatic glaucoma 9.6
2088 brain cancer 9.6
2089 porphyria 9.6
2090 loiasis 9.6
2091 hyperparathyroidism 9.6
2092 biliary atresia 9.6
2093 equatorial staphyloma 9.6
2094 staphyloma posticum 9.6
2095 squamous cell papilloma 9.6
2096 plasmodium falciparum malaria 9.6
2097 choroid disease 9.6
2098 renal tubular acidosis 9.6
2099 adult-onset still's disease 9.6
2100 lymphangioma 9.6
2101 urticaria 9.6
2102 angioedema 9.6
2103 ectropion 9.6
2104 rheumatic fever 9.6
2105 endogenous depression 9.6
2106 keratosis 9.6
2107 melanotic neuroectodermal tumor 9.6
2108 pineoblastoma 9.6
2109 pneumothorax 9.6