MCID: PRM038
MIFTS: 43

Primary Agammaglobulinemia

Categories: Blood diseases, Genetic diseases, Immune diseases, Rare diseases

Aliases & Classifications for Primary Agammaglobulinemia

Summaries for Primary Agammaglobulinemia

MalaCards based summary : Primary Agammaglobulinemia, also known as antibody deficiency syndrome, is related to immunodeficiency, common variable, 2 and common variable immunodeficiency. An important gene associated with Primary Agammaglobulinemia is TNFRSF13C (TNF Receptor Superfamily Member 13C), and among its related pathways/superpathways are Allograft rejection and TRAF Pathway. The drugs Omeprazole and Propylthiouracil have been mentioned in the context of this disorder. Affiliated tissues include breast, lung and b cells.

Wikipedia : 74 Hypogammaglobulinemia is a problem with the immune system in which not enough gamma globulins are... more...

Related Diseases for Primary Agammaglobulinemia

Diseases in the Agammaglobulinemia family:

Agammaglobulinemia 1, Autosomal Recessive Agammaglobulinemia 6, Autosomal Recessive
Agammaglobulinemia 2, Autosomal Recessive Agammaglobulinemia 3, Autosomal Recessive
Agammaglobulinemia 4, Autosomal Recessive Agammaglobulinemia 5, Autosomal Dominant
Agammaglobulinemia 7, Autosomal Recessive Agammaglobulinemia 8, Autosomal Dominant
Primary Agammaglobulinemia

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

(showing 4026, show less)
# Related Disease Score Top Affiliating Genes
1 immunodeficiency, common variable, 2 32.5 TNFRSF13C TNFRSF13B
2 common variable immunodeficiency 32.4 TNFRSF13C TNFRSF13B
3 immunoglobulin alpha deficiency 31.6 TNFRSF13C TNFRSF13B
4 cryptococcal meningitis 29.4 TNFRSF13C TNFRSF13B
5 autoimmune disease 29.2 TNFRSF13C TNFRSF13B
6 macroglobulinemia 29.1 TNFRSF13C TNFRSF13B
7 myeloma, multiple 29.1 TNFRSF13C TNFRSF13B
8 b cell deficiency 28.9 TNFRSF13C TNFRSF13B
9 leukemia, chronic lymphocytic 28.5 TNFRSF13C TNFRSF13B
10 lymphoma, non-hodgkin, familial 28.5 TNFRSF13C TNFRSF13B
11 autoinflammation, antibody deficiency, and immune dysregulation, plcg2-associated 12.7
12 specific antibody deficiency 12.7
13 limbic encephalitis with lgi1 antibodies 12.5
14 warm antibody hemolytic anemia 12.5
15 specific antibody deficiency with normal immunoglobulin concentrations and normal numbers of b cells 12.3
16 lymphopenic hypergammaglobulinemia, antibody deficiency, autoimmune hemolytic anemia, and glomerulonephritis 12.3
17 selective immunoglobulin deficiency disease 12.3
18 antiphospholipid syndrome 12.3
19 anti-pit-1 antibody syndrome 12.3
20 familial cold autoinflammatory syndrome 3 12.3
21 other immunodeficiency syndrome with predominantly antibody defects 12.2
22 alopecia antibody deficiency 12.2
23 rheumatoid factor-negative juvenile idiopathic arthritis without anti-nuclear antibodies 12.2
24 rheumatoid factor-negative juvenile idiopathic arthritis with anti-nuclear antibodies 12.2
25 oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies 12.2
26 oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies 12.2
27 limbic encephalitis with dpp6 antibodies 12.2
28 obsolete: limbic encephalitis with ncmags antibodies 12.1
29 limbic encephalitis with nmda receptor antibodies 12.1
30 immunodeficiency, common variable, 1 12.1
31 antigen defined by monoclonal antibody aj9 12.1
32 antigen defined by monoclonal antibody t87 12.1
33 limbic encephalitis associated with antibodies to cell membrane antigens 12.1
34 limbic encephalitis with caspr2 antibodies 12.1
35 polyradiculoneuropathy associated with igg/iga/igm monoclonal gammopathy without known antibodies 12.1
36 limbic encephalitis with neurexin-3 antibodies 12.1
37 response to monoclonal antibody treatment 12.1
38 congenital hypothyroidism due to transplacental passage of tsh-binding inhibitory antibodies 12.1
39 immunodeficiency, common variable, 3 12.1
40 goodpasture syndrome 12.0
41 canomad syndrome 12.0
42 cold agglutinin disease 12.0
43 immunodeficiency, common variable, 4 12.0
44 roifman syndrome 12.0
45 immunodeficiency, common variable, 6 12.0
46 immunodeficiency, common variable, 5 11.8
47 myasthenia gravis 11.8
48 thrombotic thrombocytopenic purpura, acquired 11.8
49 hemolytic uremic syndrome, atypical 1 11.6
50 pemphigus vulgaris, familial 11.6
51 granulomatosis with polyangiitis 11.6
52 stiff-person syndrome 11.6
53 antiphospholipid syndrome, familial 11.6
54 bullous pemphigoid 11.5
55 pauci-immune glomerulonephritis without anca 11.5
56 lambert-eaton myasthenic syndrome 11.5
57 monoclonal gammopathy of uncertain significance 11.5
58 blood group, cromer system 11.5
59 miller fisher syndrome 11.5
60 castleman disease 11.4
61 hirata disease 11.4
62 lymphoplasmacytic lymphoma 11.4
63 congenital myasthenic syndrome 11.4
64 yt blood group antigen 11.4
65 isolated growth hormone deficiency, type ia 11.4
66 b-cell expansion with nfkb and t-cell anergy 11.4
67 insulin-resistance type b 11.4
68 rapidly progressive glomerulonephritis 11.4
69 autoimmune encephalitis 11.4
70 catastrophic antiphospholipid syndrome 11.4
71 paraneoplastic cerebellar degeneration 11.4
72 diffuse large b-cell lymphoma 11.4
73 scleroderma, familial progressive 11.4
74 ovarian cancer 11.4
75 neonatal antiphospholipid syndrome 11.4
76 primary biliary cirrhosis 11.4
77 tropical spastic paraparesis 11.4
78 myelopathy, htlv-1-associated 11.4
79 immunoglobulin a deficiency 1 11.4
80 immunodeficiency 62 11.4
81 arthus reaction 11.3
82 al amyloidosis 11.3
83 pemphigus 11.3
84 episodic ataxia 11.3
85 agammaglobulinemia 1, autosomal recessive 11.3
86 fetal erythroblastosis 11.3
87 melanoma 11.3
88 microscopic polyangiitis 11.3
89 rh-null, amorph type 11.3
90 tn polyagglutination syndrome 11.3
91 blood group, chido/rodgers system 11.3
92 blood group, junior system 11.3
93 limbic encephalitis 11.3
94 heparin-induced thrombocytopenia 11.3
95 sjogren syndrome 11.3
96 dengue disease 11.3
97 iga glomerulonephritis 11.3
98 dilated cardiomyopathy 11.3
99 graves disease 1 11.3
100 immunodeficiency-centromeric instability-facial anomalies syndrome 1 11.2
101 immunodeficiency-centromeric instability-facial anomalies syndrome 2 11.2
102 extrinsic allergic alveolitis 11.2
103 immunodeficiency with hyper-igm, type 3 11.2
104 paraneoplastic syndromes 11.2
105 parainfluenza virus type 3 11.2
106 fetal and neonatal alloimmune thrombocytopenia 11.2
107 antisynthetase syndrome 11.2
108 subacute thyroiditis 11.2
109 acute motor axonal neuropathy 11.2
110 bickerstaff brainstem encephalitis 11.2
111 latex allergy 11.2
112 henoch-schoenlein purpura 11.2
113 lymphoma, mucosa-associated lymphoid type 11.2
114 autoimmune autonomic ganglionopathy 11.2
115 pulmonary alveolar proteinosis 11.2
116 systemic onset juvenile idiopathic arthritis 11.2
117 hypersensitivity reaction type iii disease 11.2
118 autoimmune retinopathy 11.2
119 palindromic rheumatism 11.2
120 iga nephropathy 1 11.2
121 autoimmune oophoritis 11.2
122 acquired von willebrand syndrome 11.2
123 capillary leak syndrome 11.2
124 epidermodysplasia verruciformis 1 11.2
125 paraneoplastic neurologic disorders 11.2
126 autoimmune polyendocrine syndrome, type ii 11.2
127 systemic lupus erythematosus 16 11.2
128 blood group, gerbich system 11.2
129 light chain deposition disease 11.2
130 persistent polyclonal b-cell lymphocytosis 11.2
131 pulmonary alveolar proteinosis, acquired 11.2
132 blood group, dombrock system 11.2
133 lichtenstein syndrome 11.2
134 severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency 11.2
135 blood group, langereis system 11.2
136 lutheran null 11.2
137 intrinsic factor deficiency 11.2
138 purine nucleoside phosphorylase deficiency 11.2
139 agammaglobulinemia 2, autosomal recessive 11.2
140 hyperproinsulinemia 11.2
141 salivary gland carcinoma 11.2
142 salivary gland disease 11.2
143 bone marrow cancer 11.2
144 smoldering myeloma 11.2
145 pediatric acute-onset neuropsychiatric syndrome 11.2
146 primary intestinal lymphangiectasia 11.2
147 gamma heavy chain disease 11.2
148 epilepsy with bilateral occipital calcifications 11.1
149 retinohepatoendocrinologic syndrome 11.1
150 ectodermal dysplasia and immunodeficiency 1 11.1
151 congenital disorder of glycosylation, type ig 11.1
152 blood group, globoside system 11.1
153 blood group, vel system 11.1
154 alg1-congenital disorder of glycosylation 11.1
155 pgm3-congenital disorder of glycosylation 11.1
156 trichothiodystrophy 5, nonphotosensitive 11.1
157 riddle syndrome 11.1
158 selective igm deficiency disease 11.1
159 immunodeficiency-centromeric instability-facial anomalies syndrome 11.1
160 selective igd deficiency disease 11.1
161 gait ataxia with late onset polyneuropathy syndrome 11.1
162 polyneuropathy associated with igm monoclonal gammapathy with anti-mag 11.1
163 pauci-immune glomerulonephritis with anca 11.1
164 immunodeficiency, common variable, 7 11.1
165 autoimmune lymphoproliferative syndrome, type iii 11.1
166 immunodeficiency, common variable, 11 11.1
167 immunodeficiency 36 11.1
168 immunodeficiency, common variable, 12 11.1
169 immunodeficiency, common variable, 13 11.1
170 combined cellular and humoral immune defects with granulomas 11.0
171 secretory component deficiency 11.0
172 lymphoproliferative syndrome, x-linked, 1 11.0
173 severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-negative 11.0
174 histiocytosis-lymphadenopathy plus syndrome 11.0
175 hyperthyroidism, nonautoimmune 11.0
176 ficolin 3 deficiency 11.0
177 blood group, john milton hagen system 11.0
178 lymphoproliferative syndrome 2 11.0
179 complement receptor deficiency 11.0
180 retrovirus-associated myelopathy 11.0
181 hepatitis c virus 10.9
182 hepatitis b vaccine, response to 10.9
183 thrombophilia due to protein c deficiency, autosomal dominant 10.9
184 whim syndrome 10.9
185 bare lymphocyte syndrome, type ii 10.9
186 epiphyseal dysplasia, multiple, with early-onset diabetes mellitus 10.9
187 myasthenic syndrome, congenital, 6, presynaptic 10.9
188 ataxia-telangiectasia-like disorder 1 10.9
189 autoimmune thyroid disease 3 10.9
190 myopathy, myosin storage, autosomal dominant 10.9
191 severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-positive 10.9
192 immunoglobulin a deficiency 2 10.9
193 severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation 10.9
194 agammaglobulinemia 6, autosomal recessive 10.9
195 isolated growth hormone deficiency, type ib 10.9
196 reynolds syndrome 10.9
197 agammaglobulinemia 3, autosomal recessive 10.9
198 agammaglobulinemia 4, autosomal recessive 10.9
199 agammaglobulinemia 5, autosomal dominant 10.9
200 lipodystrophy, partial, acquired, with low complement component c3, with or without glomerulonephritis 10.9
201 immunodeficiency, common variable, 8, with autoimmunity 10.9
202 agammaglobulinemia 7, autosomal recessive 10.9
203 immunodeficiency 20 10.9
204 agammaglobulinemia 8, autosomal dominant 10.9
205 autoimmune disease of endocrine system 10.9
206 janus kinase-3 deficiency 10.9
207 immunoglobulin beta deficiency 10.9
208 autoimmune disease of exocrine system 10.9
209 autoimmune disease of gastrointestinal tract 10.9
210 autoimmune disease of musculoskeletal system 10.9
211 autoimmune disease of peripheral nervous system 10.9
212 autoimmune disease of skin and connective tissue 10.9
213 autoimmune disease of urogenital tract 10.9
214 autoimmune disease of blood 10.9
215 autoimmune disease of cardiovascular system 10.9
216 mu chain disease 10.9
217 delta chain disease 10.9
218 transient neonatal diabetes mellitus 10.9
219 familial hypocalciuric hypercalcemia 10.9
220 acquired generalized lipodystrophy 10.9
221 hyaline body myopathy 10.9
222 congenital herpes simplex 10.9
223 epidermolysa bullosa simplex with muscular dystrophy 10.9
224 episodic angioedema with eosinophilia 10.9
225 localized lipodystrophy 10.9
226 pediatric autoimmune neuropsychiatric disorders associated with streptococcus infections 10.9
227 rheumatoid factor-negative juvenile idiopathic arthritis 10.9
228 salivary gland cancer, adult 10.9
229 trnt1 deficiency 10.9
230 lupus - neurological sequelae 10.9
231 familial chilblain lupus 10.9
232 hepatitis b 10.8
233 human immunodeficiency virus type 1 10.8
234 influenza 10.7
235 dengue virus 10.7
236 adenocarcinoma 10.7
237 hepatitis a 10.7
238 rheumatoid arthritis 10.7
239 hepatitis 10.7
240 syphilis 10.7
241 cholera 10.7
242 colorectal cancer 10.7
243 toxoplasmosis 10.6
244 neuroblastoma 10.6
245 breast cancer 10.6
246 mouth disease 10.6
247 mumps 10.6
248 liver cirrhosis 10.6
249 vaccinia 10.6
250 neuropathy 10.6
251 multiple sclerosis 10.6
252 thrombophilia due to thrombin defect 10.6
253 infertility 10.6
254 t-cell leukemia 10.6
255 cytokine deficiency 10.6
256 schistosoma mansoni infection, susceptibility/ 10.6
257 schistosomiasis 10.6
258 newcastle disease 10.6
259 avian influenza 10.6
260 pancreatic cancer 10.6
261 thrombosis 10.6
262 japanese encephalitis 10.6
263 leukemia, acute lymphoblastic 10.5
264 diabetes mellitus, insulin-dependent 10.5
265 pfeiffer syndrome 10.5
266 rheumatic disease 10.5
267 glioma 10.5
268 glial tumor 10.5
269 hemophilia 10.5
270 viral hepatitis 10.5
271 kala-azar 1 10.5
272 leishmaniasis 10.5
273 nasopharyngeal carcinoma 10.5
274 neuritis 10.5
275 west nile virus 10.5
276 leukemia, acute myeloid 10.5
277 polymyositis 10.5
278 malaria 10.5
279 polyneuropathy 10.5
280 raynaud phenomenon 10.5
281 brucellosis 10.5
282 typhoid fever 10.5
283 thyroid carcinoma 10.5
284 glioblastoma multiforme 10.5
285 chagas disease 10.5
286 lung cancer 10.5
287 optic neuritis 10.5
288 dermatitis, atopic 10.5
289 severe acute respiratory syndrome 10.5
290 myopathy 10.5
291 chlamydia pneumonia 10.5
292 crescentic glomerulonephritis 10.5
293 goiter 10.5
294 myelitis 10.5
295 stomatitis 10.5
296 cytomegalovirus infection 10.5
297 bladder cancer 10.5
298 membranous nephropathy 10.5
299 end stage renal failure 10.5
300 thyroid gland disease 10.5
301 hepatocellular carcinoma 10.4
302 pre-eclampsia 10.4
303 small cell cancer of the lung 10.4
304 renal cell carcinoma, nonpapillary 10.4
305 encephalopathy 10.4
306 demyelinating disease 10.4
307 anthrax disease 10.4
308 inflammatory spondylopathy 10.4
309 spondylitis 10.4
310 adult t-cell leukemia 10.4
311 agammaglobulinemia 10.4
312 spondyloarthropathy 1 10.4
313 factor viii deficiency 10.4
314 hemophilia a 10.4
315 myocarditis 10.4
316 alzheimer disease 10.4
317 osteogenic sarcoma 10.4
318 leptospirosis 10.4
319 filariasis 10.4
320 immunodeficiency predominantly affecting antibody production 10.4
321 yellow fever 10.4
322 lung cancer susceptibility 3 10.4
323 vascular disease 10.4
324 idiopathic interstitial pneumonia 10.4
325 atherosclerosis susceptibility 10.4
326 squamous cell carcinoma 10.4
327 peripheral nervous system disease 10.4
328 pulmonary tuberculosis 10.4
329 prostate cancer 10.4
330 pulmonary fibrosis 10.4
331 acute leukemia 10.4
332 aspergillosis 10.4
333 dengue hemorrhagic fever 10.4
334 rheumatic fever 10.4
335 adenoma 10.4
336 aceruloplasminemia 10.4
337 plague 10.4
338 smallpox 10.4
339 enthesopathy 10.4
340 rapidly involuting congenital hemangioma 10.4
341 papillomatosis, confluent and reticulated 10.4
342 benign mesothelioma 10.4
343 lateral sclerosis 10.4
344 amyotrophic lateral sclerosis 1 10.4
345 urticaria 10.4
346 cerebellar degeneration 10.4
347 variola major 10.4
348 psoriatic arthritis 10.4
349 migraine with or without aura 1 10.4
350 helicobacter pylori infection 10.4
351 relapsing-remitting multiple sclerosis 10.4
352 transverse myelitis 10.4
353 kidney disease 10.4
354 visceral leishmaniasis 10.4
355 hypoglycemia 10.4
356 australia antigen 10.4
357 epidemic typhus 10.4
358 cysticercosis 10.4
359 pyelonephritis 10.4
360 cervical cancer 10.3
361 neuromyelitis optica spectrum disorder 10.3
362 acute graft versus host disease 10.3
363 churg-strauss syndrome 10.3
364 helix syndrome 10.3
365 stroke, ischemic 10.3
366 chikungunya 10.3
367 peritonitis 10.3
368 plasmodium falciparum malaria 10.3
369 lymphocytic choriomeningitis 10.3
370 chorea, childhood-onset, with psychomotor retardation 10.3
371 small cell carcinoma 10.3
372 choreatic disease 10.3
373 respiratory failure 10.3
374 immunodeficiency with hyper-igm, type 5 10.3
375 immunodeficiency with hyper-igm, type 4 10.3
376 cerebrovascular disease 10.3
377 polyarteritis nodosa 10.3
378 hemolytic-uremic syndrome 10.3
379 demyelinating polyneuropathy 10.3
380 human immunodeficiency virus infectious disease 10.3
381 suppressor of tumorigenicity 3 10.3
382 dysentery 10.3
383 ischemia 10.3
384 prion disease 10.3
385 pulmonary embolism 10.3
386 collagen disease 10.3
387 kearns-sayre syndrome 10.3
388 triiodothyronine receptor auxiliary protein 10.3
389 bone resorption disease 10.3
390 echinococcosis 10.3
391 hypercholesterolemia, familial, 1 10.3
392 meningoencephalitis 10.3
393 spotted fever 10.3
394 multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly 10.3
395 trypanosomiasis 10.3
396 colon adenocarcinoma 10.3
397 myoclonus 10.3
398 fibrosarcoma 10.3
399 lepromatous leprosy 10.3
400 teratoma 10.3
401 acute kidney failure 10.3
402 thrombophilia 10.3
403 hairy cell leukemia 10.3
404 dermatitis herpetiformis, familial 10.3
405 dermatitis herpetiformis 10.3
406 choriocarcinoma 10.3
407 placenta disease 10.3
408 thrombotic thrombocytopenic purpura 10.3
409 papilloma 10.3
410 insulinoma 10.3
411 leukemia, acute lymphoblastic 3 10.3
412 allergic angiitis 10.3
413 argyria 10.3
414 swine influenza 10.2
415 progressive multifocal leukoencephalopathy 10.2
416 genital herpes 10.2
417 asthma 10.2
418 chronic inflammatory demyelinating polyradiculoneuropathy 10.2
419 heart block, congenital 10.2
420 eclampsia 10.2
421 arthropathy 10.2
422 hyperglycemia 10.2
423 thalassemia 10.2
424 myocardial infarction 10.2
425 mastitis 10.2
426 systemic autoimmune disease 10.2
427 cholangitis, primary sclerosing 10.2
428 rift valley fever 10.2
429 mesothelioma, malignant 10.2
430 insulin-like growth factor i 10.2
431 volvulus of midgut 10.2
432 scrapie 10.2
433 precursor t-cell acute lymphoblastic leukemia 10.2
434 thrombotic microangiopathy 10.2
435 peptic ulcer disease 10.2
436 proliferative glomerulonephritis 10.2
437 eye disease 10.2
438 cutaneous leishmaniasis 10.2
439 endometrial cancer 10.2
440 coronary artery anomaly 10.2
441 hepatitis d 10.2
442 coronary heart disease 1 10.2
443 transitional cell carcinoma 10.2
444 reactive arthritis 10.2
445 erythroleukemia, familial 10.2
446 ornithosis 10.2
447 duodenal ulcer 10.2
448 acute disseminated encephalomyelitis 10.2
449 acute myocardial infarction 10.2
450 pemphigus foliaceus 10.2
451 spastic paraparesis 10.2
452 pollen allergy 10.2
453 autoimmune gastrointestinal dysmotility 10.2
454 ovarian epithelial cancer 10.2
455 myelodysplastic syndrome 10.2
456 hyperlipoproteinemia, type iii 10.2
457 endometriosis 10.2
458 trichinosis 10.2
459 obsolete: squamous cell carcinoma of head and neck 10.2
460 esophageal cancer 10.2
461 heart disease 10.2
462 alpha/beta t-cell lymphopenia with gamma/delta t-cell expansion, severe cytomegalovirus infection, and autoimmunity 10.2
463 arteries, anomalies of 10.2
464 aplastic anemia 10.2
465 pulmonary fibrosis and/or bone marrow failure, telomere-related, 2 10.2
466 motor neuron disease 10.2
467 rhabdomyosarcoma 10.2
468 atrial standstill 1 10.2
469 teratocarcinoma 10.2
470 cutaneous t cell lymphoma 10.2
471 salmonellosis 10.2
472 squamous cell papilloma 10.2
473 astrocytoma 10.2
474 malignant glioma 10.2
475 diabetes mellitus, noninsulin-dependent 10.2
476 fibrosis of extraocular muscles, congenital, 1 10.2
477 mycosis fungoides 10.2
478 squamous cell carcinoma, head and neck 10.2
479 crest syndrome 10.2
480 sensory peripheral neuropathy 10.2
481 lymphosarcoma 10.2
482 macular degeneration, age-related, 1 10.2
483 mantle cell lymphoma 10.2
484 toxocariasis 10.2
485 dysphagia 10.2
486 filarial elephantiasis 10.2
487 histoplasmosis 10.2
488 bronchiolitis obliterans 10.2
489 yemenite deaf-blind hypopigmentation syndrome 10.2
490 foodborne botulism 10.2
491 axonal neuropathy 10.2
492 iridocyclitis 10.2
493 multifocal motor neuropathy 10.2
494 human herpesvirus 8 10.2
495 intestinal schistosomiasis 10.2
496 pancreatic adenocarcinoma 10.2
497 amebiasis 10.2
498 cryptococcosis 10.2
499 osteoarthritis 10.2
500 cervix uteri carcinoma in situ 10.2
501 cervical intraepithelial neoplasia 10.2
502 htlv-1 associated myelopathy/tropical spastic paraparesis 10.2
503 lichen planus 10.2
504 osteoporosis 10.2
505 korean hemorrhagic fever 10.2
506 hand, foot and mouth disease 10.2
507 congenital toxoplasmosis 10.2
508 hemoglobinuria 10.2
509 chronic kidney disease 10.2
510 spinal cord injury 10.2
511 kawasaki disease 10.2
512 cutaneous lupus erythematosus 10.2
513 onchocerciasis 10.2
514 male infertility 10.2
515 von willebrand's disease 10.2
516 crohn's colitis 10.2
517 ehrlichiosis 10.2
518 st. louis encephalitis 10.2
519 status epilepticus 10.2
520 kidney cancer 10.2
521 agammaglobulinemia, non-bruton type 10.2
522 hyper-igm syndrome without susceptibility to opportunistic infections 10.2
523 hyper-igm syndrome with susceptibility to opportunistic infections 10.2
524 schizophrenia 10.2
525 hantavirus hemorrhagic fever with renal syndrome 10.2
526 calcinosis 10.2
527 tularemia 10.2
528 colorectal adenocarcinoma 10.2
529 pulmonary edema 10.2
530 urethritis 10.2
531 movement disease 10.2
532 rheumatic fever-related antigen 10.2
533 bacteriuria 10.2
534 dystonia 10.2
535 thrombasthenia 10.2
536 disseminated intravascular coagulation 10.1
537 pancreatic ductal adenocarcinoma 10.1
538 viral infectious disease 10.1
539 human t-cell leukemia virus type 1 10.1
540 creutzfeldt-jakob disease 10.1
541 allergic bronchopulmonary aspergillosis 10.1
542 chronic fatigue syndrome 10.1
543 pachyonychia congenita 3 10.1
544 western equine encephalitis 10.1
545 paracoccidioidomycosis 10.1
546 in situ carcinoma 10.1
547 babesiosis 10.1
548 dengue shock syndrome 10.1
549 breast adenocarcinoma 10.1
550 mast cell neoplasm 10.1
551 extracutaneous mastocytoma 10.1
552 bone mineral density quantitative trait locus 8 10.1
553 bone mineral density quantitative trait locus 15 10.1
554 atrioventricular block 10.1
555 sleeping sickness 10.1
556 prostatic hypertrophy 10.1
557 borna disease 10.1
558 retinoblastoma 10.1
559 melioidosis 10.1
560 trachoma 10.1
561 farmer's lung 10.1
562 familial retinoblastoma 10.1
563 venezuelan equine encephalitis 10.1
564 down syndrome 10.1
565 pancytopenia 10.1
566 acute pancreatitis 10.1
567 aleutian mink disease 10.1
568 embryonal carcinoma 10.1
569 intermediate coronary syndrome 10.1
570 tremor 10.1
571 interstitial nephritis 10.1
572 polyradiculoneuropathy 10.1
573 localized scleroderma 10.1
574 discoid lupus erythematosus 10.1
575 asplenia, isolated congenital 10.1
576 hydrops, lactic acidosis, and sideroblastic anemia 10.1
577 scrub typhus 10.1
578 nervous system disease 10.1
579 legionnaire disease 10.1
580 inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 10.1
581 inclusion body myopathy with early-onset paget disease of bone with or without frontotemporal dementia 2 10.1
582 histiocytosis 10.1
583 rheumatic heart disease 10.1
584 angioedema 10.1
585 chronic graft versus host disease 10.1
586 obsolete: rapidly progressive glomerulonephritis 10.1
587 pulmonary hypertension, primary, 1 10.1
588 gastric ulcer 10.1
589 fascioliasis 10.1
590 pulmonary fibrosis, idiopathic 10.1
591 lipid metabolism disorder 10.1
592 central nervous system disease 10.1
593 heart valve disease 10.1
594 polykaryocytosis inducer 10.1
595 ptosis 10.1
596 hemorrhagic disease 10.1
597 homologous wasting disease 10.1
598 bacterial infectious disease 10.1
599 pheochromocytoma 10.1
600 leukemia, chronic myeloid 10.1
601 anaplastic large cell lymphoma 10.1
602 adrenal gland pheochromocytoma 10.1
603 pelvic inflammatory disease 10.1
604 familial hypercholesterolemia 10.1
605 cholangiocarcinoma 10.1
606 asymptomatic neurosyphilis 10.1
607 paragonimiasis 10.1
608 pleuropneumonia 10.1
609 optic nerve disease 10.1
610 immune-complex glomerulonephritis 10.1
611 pancreatitis 10.1
612 neurosyphilis 10.1
613 hair whorl 10.1
614 listeriosis 10.1
615 pericarditis 10.1
616 constipation 10.1
617 pharyngitis 10.1
618 arteriosclerosis 10.1
619 prostatic adenoma 10.1
620 intrahepatic cholangiocarcinoma 10.1
621 irritable bowel syndrome 10.1
622 headache 10.1
623 teratoma, ovarian 10.1
624 microvascular complications of diabetes 3 10.1
625 microvascular complications of diabetes 4 10.1
626 microvascular complications of diabetes 6 10.1
627 microvascular complications of diabetes 7 10.1
628 coronavirus infection 10.1
629 basal cell carcinoma 10.1
630 ebola hemorrhagic fever 10.1
631 seminoma 10.1
632 ovarian germ cell teratoma 10.1
633 congestive heart failure 10.1
634 b-cell growth factor 10.1
635 pregnancy loss, recurrent 1 10.1
636 neuroretinitis 10.1
637 herpes simplex encephalitis 10.1
638 mast cell activation syndrome 10.1
639 meningococcal infection 10.1
640 oral cancer 10.1
641 cryoglobulinemia, familial mixed 10.1
642 gestational diabetes 10.1
643 alcoholic hepatitis 10.1
644 breast disease 10.1
645 microvascular complications of diabetes 5 10.1
646 shigellosis 10.1
647 facial paralysis 10.1
648 cystic echinococcosis 10.1
649 retinitis 10.1
650 epidermolysis bullosa acquisita 10.1
651 b-cell non-hodgkin lymphoma 10.1
652 huntington disease 10.1
653 infective endocarditis 10.1
654 microcephaly 10.1
655 ovary adenocarcinoma 10.1
656 neonatal lupus erythematosus 10.1
657 acute liver failure 10.1
658 transient pseudohypoaldosteronism 10.1
659 thyroid cancer, nonmedullary, 1 10.1
660 hemophilia b 10.1
661 prostatic hyperplasia, benign 10.1
662 lymphadenitis 10.1
663 mammary paget's disease 10.1
664 mesangial proliferative glomerulonephritis 10.1
665 exophthalmos 10.1
666 pathologic nystagmus 10.1
667 undifferentiated connective tissue disease 10.1
668 dysautonomia 10.1
669 erysipelas 10.1
670 pyoderma 10.1
671 viral encephalitis 10.1
672 lung disease 10.1
673 periodontitis, chronic 10.1
674 mycobacterium tuberculosis 1 10.1
675 paroxysmal nocturnal hemoglobinuria 10.1
676 eastern equine encephalitis 10.1
677 fibromyalgia 10.1
678 fatty liver disease 10.1
679 acquired hemophilia 10.1
680 chondrosarcoma 10.0
681 myxedema 10.0
682 angina pectoris 10.0
683 cervical dystonia 10.0
684 zika fever 10.0
685 bone disease 10.0
686 amnestic disorder 10.0
687 cat-scratch disease 10.0
688 diffuse scleroderma 10.0
689 temporal lobe epilepsy 10.0
690 thyroid gland papillary carcinoma 10.0
691 hemolytic disease due to fetomaternal alloimmunization 10.0
692 oral squamous cell carcinoma 10.0
693 autonomic dysfunction 10.0
694 medulloblastoma 10.0
695 blastomycosis 10.0
696 severe pre-eclampsia 10.0
697 chronic granulomatous disease 10.0
698 acute pyelonephritis 10.0
699 skin melanoma 10.0
700 differentiated thyroid carcinoma 10.0
701 diffuse alveolar hemorrhage 10.0
702 glomerular disease 10.0
703 neutropenia 10.0
704 wilms tumor 5 10.0
705 branchiootic syndrome 1 10.0
706 homocysteinemia 10.0
707 meningioma, radiation-induced 10.0
708 inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 10.0
709 laryngotracheitis 10.0
710 inclusion body myopathy with early-onset paget disease of bone with or without frontotemporal dementia 3 10.0
711 bilirubin metabolic disorder 10.0
712 thrombophilia due to activated protein c resistance 10.0
713 transient cerebral ischemia 10.0
714 relapsing polychondritis 10.0
715 large cell carcinoma 10.0
716 thyroid carcinoma, familial medullary 10.0
717 meningioma, familial 10.0
718 hypotrichosis and recurrent skin vesicles 10.0
719 beta-thalassemia 10.0
720 pleurisy 10.0
721 murray valley encephalitis 10.0
722 strongyloidiasis 10.0
723 spinal meningioma 10.0
724 prostatitis 10.0
725 coccidiosis 10.0
726 thrombophlebitis 10.0
727 neuromuscular disease 10.0
728 secretory meningioma 10.0
729 lymphoplasmacyte-rich meningioma 10.0
730 cataract 10.0
731 chorioretinitis 10.0
732 soft tissue sarcoma 10.0
733 paraneoplastic limbic encephalitis 10.0
734 obsolete: small pox 10.0
735 pik3ca-related overgrowth syndrome 10.0
736 ocular cicatricial pemphigoid 10.0
737 ascaris lumbricoides infection 10.0
738 peripheral vascular disease 10.0
739 invasive aspergillosis 10.0
740 prolymphocytic leukemia 10.0
741 legionellosis 10.0
742 chronic pyelonephritis 10.0
743 crimean-congo hemorrhagic fever 10.0
744 rectum cancer 10.0
745 lung squamous cell carcinoma 10.0
746 primary syphilis 10.0
747 salpingitis 10.0
748 monocytic leukemia 10.0
749 diabetes insipidus 10.0
750 subacute cutaneous lupus erythematosus 10.0
751 haemophilus influenzae 10.0
752 neurofibromatosis, type ii 10.0
753 common cold 10.0
754 focal segmental glomerulosclerosis 10.0
755 eosinophilic pneumonia 10.0
756 malignant pleural mesothelioma 10.0
757 muscular dystrophy, duchenne type 10.0
758 intraocular pressure quantitative trait locus 10.0
759 gastrointestinal carcinoma 10.0
760 cerebral artery occlusion 10.0
761 tuberculoid leprosy 10.0
762 iron deficiency anemia 10.0
763 dementia 10.0
764 thyroid gland medullary carcinoma 10.0
765 hypopituitarism 10.0
766 ocular toxoplasmosis 10.0
767 paraneoplastic pemphigus 10.0
768 pauci-immune glomerulonephritis 10.0
769 agammaglobulinemia, x-linked 10.0
770 splenomegaly 10.0
771 budd-chiari syndrome 10.0
772 langerhans cell histiocytosis 10.0
773 hemopericardium 10.0
774 pericardial effusion 10.0
775 acute poststreptococcal glomerulonephritis 10.0
776 azoospermia 10.0
777 retinal vascular disease 10.0
778 secondary syphilis 10.0
779 histiocytoma 10.0
780 muscular atrophy 10.0
781 pyoderma gangrenosum 10.0
782 cowpox 10.0
783 aneurysm 10.0
784 overgrowth syndrome 10.0
785 immune deficiency disease 10.0
786 ewing sarcoma 10.0
787 acute promyelocytic leukemia 10.0
788 autoimmune uveitis 10.0
789 penicillin allergy 10.0
790 nasopharyngitis 10.0
791 cicatricial pemphigoid 10.0
792 keratosis 10.0
793 trichomoniasis 10.0
794 thrombocytosis 10.0
795 tic disorder 10.0
796 papillary carcinoma 10.0
797 giardiasis 10.0
798 sickle cell anemia 10.0
799 gastrointestinal stromal tumor 10.0
800 bacterial sepsis 10.0
801 marginal zone b-cell lymphoma 10.0
802 mucositis 10.0
803 lymphogranuloma venereum 10.0
804 mood disorder 10.0
805 mucocutaneous leishmaniasis 10.0
806 brain injury 10.0
807 obsessive-compulsive disorder 10.0
808 autoimmune pancreatitis 10.0
809 lymphoblastic lymphoma 10.0
810 hypoparathyroidism 10.0
811 esophagitis 10.0
812 clonorchiasis 10.0
813 protein s deficiency 10.0
814 cervicitis 10.0
815 fibrous histiocytoma 10.0
816 vascular dementia 10.0
817 depression 10.0
818 inclusion body myositis 10.0
819 parkinson disease, late-onset 10.0
820 enterocolitis 10.0
821 retinal vasculitis 10.0
822 egg allergy 10.0
823 sleep disorder 10.0
824 bacterial pneumonia 10.0
825 narcolepsy 10.0
826 alcohol dependence 10.0
827 melanoma, uveal 10.0
828 sneddon syndrome 10.0
829 glycogen storage disease ii 10.0
830 hydrops fetalis, nonimmune 10.0
831 rocky mountain spotted fever 10.0
832 secondary progressive multiple sclerosis 10.0
833 ectopic pregnancy 10.0
834 glucose intolerance 10.0
835 spondyloarthropathy 10.0
836 adult respiratory distress syndrome 10.0
837 acute kidney tubular necrosis 10.0
838 alcohol use disorder 10.0
839 focal epilepsy 10.0
840 orchitis 10.0
841 ascaridiasis 10.0
842 monkeypox 10.0
843 ovarian cyst 10.0
844 erythema infectiosum 10.0
845 pulmonary eosinophilia 10.0
846 latent syphilis 10.0
847 lassa fever 10.0
848 paresthesia 10.0
849 hypertension, essential 10.0
850 fabry disease 10.0
851 mucopolysaccharidosis-plus syndrome 10.0
852 autoimmune gastritis 10.0
853 varicocele 10.0
854 scleritis 10.0
855 hantavirus pulmonary syndrome 10.0
856 nonspecific interstitial pneumonia 10.0
857 grade iii astrocytoma 10.0
858 acute t cell leukemia 10.0
859 paraplegia 10.0
860 congenital cytomegalovirus 10.0
861 undifferentiated pleomorphic sarcoma 10.0
862 chronic pain 10.0
863 posttransplant acute limbic encephalitis 10.0
864 felty syndrome 9.9
865 immunoglobulin e concentration, serum 9.9
866 retinal detachment 9.9
867 neural tube defects 9.9
868 acrocallosal syndrome 9.9
869 bernard-soulier syndrome 9.9
870 reticuloendotheliosis, x-linked 9.9
871 hypophosphatemia 9.9
872 nodular goiter 9.9
873 boutonneuse fever 9.9
874 breast fibroadenoma 9.9
875 retinal vein occlusion 9.9
876 malignant fibroxanthoma 9.9
877 larynx cancer 9.9
878 neurilemmoma 9.9
879 merkel cell carcinoma 9.9
880 t-cell adult acute lymphocytic leukemia 9.9
881 congenital syphilis 9.9
882 oral lichen planus 9.9
883 otitis media 9.9
884 lymphopenia 9.9
885 takayasu arteritis 9.9
886 major affective disorder 8 9.9
887 major affective disorder 9 9.9
888 acute diarrhea 9.9
889 angiostrongyliasis 9.9
890 persistent generalized lymphadenopathy 9.9
891 childhood acute lymphocytic leukemia 9.9
892 autonomic neuropathy 9.9
893 alveolar echinococcosis 9.9
894 opisthorchiasis 9.9
895 contact dermatitis 9.9
896 endometrial adenocarcinoma 9.9
897 bipolar disorder 9.9
898 aortic aneurysm 9.9
899 acute myocarditis 9.9
900 bladder urothelial carcinoma 9.9
901 scarlet fever 9.9
902 acute monoblastic leukemia 9.9
903 neutrophil migration 9.9
904 myelofibrosis 9.9
905 supranuclear palsy, progressive, 1 9.9
906 diabetes mellitus, ketosis-prone 9.9
907 peripheral t-cell lymphoma 9.9
908 autoimmune neuropathy 9.9
909 louping ill 9.9
910 silicosis 9.9
911 posterior uveitis 9.9
912 plasmodium vivax malaria 9.9
913 gout 9.9
914 cystadenocarcinoma 9.9
915 elephantiasis 9.9
916 progressive encephalomyelitis with rigidity and myoclonus 9.9
917 cerebral amyloid angiopathy, cst3-related 9.9
918 multiple system atrophy 1 9.9
919 human granulocytic anaplasmosis 9.9
920 osteonecrosis 9.9
921 polycystic ovary syndrome 9.9
922 hellp syndrome 9.9
923 pulmonary sarcoidosis 9.9
924 childhood type dermatomyositis 9.9
925 hyperinsulinism 9.9
926 hemoglobinopathy 9.9
927 clear cell renal cell carcinoma 9.9
928 placental abruption 9.9
929 lymphocytic hypophysitis 9.9
930 neonatal herpes 9.9
931 traumatic brain injury 9.9
932 pouchitis 9.9
933 digitalis poisoning 9.9
934 sarcoma, synovial 9.9
935 suppression of tumorigenicity 12 9.9
936 fibroma 9.9
937 parotitis 9.9
938 brain cancer 9.9
939 glanders 9.9
940 inclusion conjunctivitis 9.9
941 vaginitis 9.9
942 hemangioma 9.9
943 placental insufficiency 9.9
944 tick infestation 9.9
945 uremia 9.9
946 brain edema 9.9
947 dermatophytosis 9.9
948 autoimmune myocarditis 9.9
949 necrotizing autoimmune myopathy 9.9
950 autoimmune hepatitis type 2 9.9
951 vasculitis 9.9
952 melanoma tumor antigen gp90 9.9
953 frontotemporal dementia 9.9
954 gastrointestinal ulceration, recurrent, with dysfunctional platelets 9.9
955 open-angle glaucoma 9.9
956 ovarian disease 9.9
957 portal vein thrombosis 9.9
958 leiomyoma 9.9
959 hyperparathyroidism 9.9
960 campylobacteriosis 9.9
961 neonatal myasthenia gravis 9.9
962 serous cystadenocarcinoma 9.9
963 intracranial thrombosis 9.9
964 fasciitis 9.9
965 chromosomal triplication 9.9
966 rheumatoid vasculitis 9.9
967 cancer-associated retinopathy 9.9
968 undetermined colitis 9.9
969 pneumonia 9.9
970 acanthosis nigricans 9.9
971 behcet syndrome 9.9
972 blood group--kell system 9.9
973 raynaud disease 9.9
974 reticulum cell sarcoma 9.9
975 taeniasis 9.9
976 primary progressive multiple sclerosis 9.9
977 microinvasive gastric cancer 9.9
978 lipoid nephrosis 9.9
979 allergic conjunctivitis 9.9
980 gnathomiasis 9.9
981 mononeuropathy 9.9
982 mycoplasma pneumoniae pneumonia 9.9
983 panniculitis 9.9
984 neuroendocrine tumor 9.9
985 cerebral palsy 9.9
986 amyloidosis aa 9.9
987 gnathostoma infection 9.9
988 gilles de la tourette syndrome 9.9
989 varicose veins 9.9
990 angiosarcoma 9.9
991 sclerosteosis 9.9
992 drug allergy 9.9
993 cytomegalovirus retinitis 9.9
994 igg4-related disease 9.9
995 malignant hypertension 9.9
996 alport syndrome 9.9
997 pasteurellosis 9.9
998 coronary thrombosis 9.9
999 bell's palsy 9.9
1000 cardiovascular system disease 9.9
1001 relapsing fever 9.9
1002 iritis 9.9
1003 hereditary angioedema 9.9
1004 ocular melanoma 9.9
1005 protein c deficiency 9.9
1006 carcinosarcoma 9.9
1007 anti-basement membrane glomerulonephritis 9.9
1008 aortitis 9.9
1009 anisakiasis 9.9
1010 appendicitis 9.9
1011 amaurosis fugax 9.9
1012 opsoclonus-myoclonus syndrome 9.9
1013 paroxysmal cold hemoglobinuria 9.9
1014 pure autonomic failure 9.9
1015 hypoxia 9.9
1016 pituitary tumors 9.9
1017 glioma susceptibility 1 9.9
1018 wilms tumor 1 9.9
1019 hydatidiform mole, recurrent, 1 9.9
1020 aging 9.9
1021 microvascular complications of diabetes 1 9.9
1022 alkuraya-kucinskas syndrome 9.9
1023 autoimmune vasculitis 9.9
1024 erythema multiforme 9.9
1025 non-alcoholic steatohepatitis 9.9
1026 multicentric castleman disease 9.9
1027 panuveitis 9.9
1028 adult-onset still's disease 9.9
1029 sporotrichosis 9.9
1030 limited scleroderma 9.9
1031 neuroendocrine carcinoma 9.9
1032 vulvovaginitis 9.9
1033 splenic infarction 9.9
1034 cervix carcinoma 9.9
1035 testicular cancer 9.9
1036 breast ductal carcinoma 9.9
1037 oligodendroglioma 9.9
1038 junctional epidermolysis bullosa 9.9
1039 mesenchymal cell neoplasm 9.9
1040 pituitary adenoma 9.9
1041 macular retinal edema 9.9
1042 malignant histiocytosis 9.9
1043 gas gangrene 9.9
1044 linear scleroderma 9.9
1045 cryptogenic cirrhosis 9.9
1046 obsolete: atypical teratoid/rhabdoid tumor 9.9
1047 congenital amyoplasia 9.9
1048 iga pemphigus 9.9
1049 interstitial lung disease 9.9
1050 combined t cell and b cell immunodeficiency 9.9
1051 buerger disease 9.9
1052 autoimmune lymphoproliferative syndrome 9.9
1053 adrenal cortical carcinoma 9.9
1054 drug-induced lupus erythematosus 9.9
1055 multinodular goiter 9.9
1056 metabolic acidosis 9.9
1057 ductal carcinoma in situ 9.9
1058 non-alcoholic fatty liver disease 9.9
1059 polycystic kidney disease 9.9
1060 osteomalacia 9.9
1061 anogenital venereal wart 9.9
1062 phlebotomus fever 9.9
1063 carotid stenosis 9.9
1064 chancroid 9.9
1065 glossitis 9.9
1066 mental depression 9.9
1067 west nile encephalitis 9.9
1068 gestational trophoblastic neoplasm 9.9
1069 theileriasis 9.9
1070 amelanotic melanoma 9.9
1071 peanut allergy 9.9
1072 subacute bacterial endocarditis 9.9
1073 retinal disease 9.9
1074 hodgkin's lymphoma, lymphocytic-histiocytic predominance 9.9
1075 plasma cell leukemia 9.9
1076 acquired hemophilia a 9.9
1077 linear iga disease 9.9
1078 lymphoma aids related 9.9
1079 streptococcal group a invasive disease 9.9
1080 hepatic veno-occlusive disease 9.9
1081 tetanus 9.9
1082 diarrhea 9.9
1083 synovitis 9.9
1084 liver disease 9.9
1085 juvenile rheumatoid arthritis 9.9
1086 septic arthritis 9.9
1087 arthritis 9.9
1088 amyloidosis 9.9
1089 bronchiectasis 9.9
1090 48,xyyy 9.9
1091 glaucoma, primary open angle 9.8
1092 hypertriglyceridemia, familial 9.8
1093 lentigines 9.8
1094 leukemia, acute monocytic 9.8
1095 endocardial fibroelastosis 9.8
1096 glanzmann thrombasthenia 9.8
1097 hyperprolactinemia 9.8
1098 mulchandani-bhoj-conlin syndrome 9.8
1099 familial adenomatous polyposis 9.8
1100 respiratory syncytial virus infectious disease 9.8
1101 autoimmune polyendocrine syndrome 9.8
1102 pemphigoid gestationis 9.8
1103 atrophic glossitis 9.8
1104 mononeuritis multiplex 9.8
1105 papillary adenocarcinoma 9.8
1106 lysosomal storage disease 9.8
1107 liposarcoma 9.8
1108 hypokalemia 9.8
1109 bile duct cancer 9.8
1110 atrophic rhinitis 9.8
1111 aortic valve insufficiency 9.8
1112 cocaine abuse 9.8
1113 retinal degeneration 9.8
1114 acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22) 9.8
1115 binswanger's disease 9.8
1116 cholelithiasis 9.8
1117 aortic aneurysm, familial abdominal, 1 9.8
1118 hypercarotenemia and vitamin a deficiency, autosomal dominant 9.8
1119 cryptorchidism, unilateral or bilateral 9.8
1120 brittle bone disorder 9.8
1121 esophagitis, eosinophilic, 1 9.8
1122 cardiac arrest 9.8
1123 xerophthalmia 9.8
1124 keratomalacia 9.8
1125 mitral valve insufficiency 9.8
1126 ancylostomiasis 9.8
1127 pancreas disease 9.8
1128 intestinal pseudo-obstruction 9.8
1129 blood group incompatibility 9.8
1130 colonic disease 9.8
1131 back pain 9.8
1132 acute sensory ataxic neuropathy 9.8
1133 benign idiopathic neonatal seizures 9.8
1134 pneumococcal meningitis 9.8
1135 pediatric systemic lupus erythematosus 9.8
1136 digeorge syndrome 9.8
1137 allergic rhinitis 9.8
1138 exanthem 9.8
1139 diphtheria 9.8
1140 selective igg deficiency disease 9.8
1141 gastritis 9.8
1142 rhinitis 9.8
1143 severe combined immunodeficiency 9.8
1144 atrophic gastritis 9.8
1145 immunoglobulin g deficiency 9.8
1146 leukocyte adhesion deficiency, type i 9.8
1147 meniere disease 9.8
1148 pick disease of brain 9.8
1149 adrenocortical carcinoma, hereditary 9.8
1150 halothane hepatitis 9.8
1151 3-methylglutaconic aciduria, type iii 9.8
1152 muscular dystrophy, becker type 9.8
1153 microvascular complications of diabetes 2 9.8
1154 retinal dystrophy, iris coloboma, and comedogenic acne syndrome 9.8
1155 adenoid cystic carcinoma 9.8
1156 angioimmunoblastic t-cell lymphoma 9.8
1157 corneal disease 9.8
1158 acute salpingitis 9.8
1159 tetanus neonatorum 9.8
1160 bird fancier's lung 9.8
1161 renovascular hypertension 9.8
1162 thyroid gland cancer 9.8
1163 endodermal sinus tumor 9.8
1164 acrodermatitis 9.8
1165 mucinous adenocarcinoma 9.8
1166 cervical squamous cell carcinoma 9.8
1167 shwartzman phenomenon 9.8
1168 adrenal cortical adenocarcinoma 9.8
1169 coronary stenosis 9.8
1170 encephalitozoonosis 9.8
1171 intracranial hypertension 9.8
1172 myotonic dystrophy 9.8
1173 hypertrophic cardiomyopathy 9.8
1174 diffuse cutaneous systemic sclerosis 9.8
1175 mycobacterium kansasii 9.8
1176 spondylarthropathy 9.8
1177 head injury 9.8
1178 spasticity 9.8
1179 acute transverse myelitis 9.8
1180 avascular necrosis 9.8
1181 primary hypophysitis 9.8
1182 pancreatic agenesis 1 9.8
1183 retinitis pigmentosa 9.8
1184 spermatogenic failure 3 9.8
1185 major depressive disorder 9.8
1186 schuurs-hoeijmakers syndrome 9.8
1187 la crosse encephalitis 9.8
1188 nodal marginal zone lymphoma 9.8
1189 sialadenitis 9.8
1190 viral meningitis 9.8
1191 kuhnt-junius degeneration 9.8
1192 hemiplegia 9.8
1193 amenorrhea 9.8
1194 autosomal dominant cerebellar ataxia 9.8
1195 inner ear disease 9.8
1196 appendix adenocarcinoma 9.8
1197 epidermolysis bullosa dystrophica 9.8
1198 paget's disease of bone 9.8
1199 plasma cell neoplasm 9.8
1200 scabies 9.8
1201 ileus 9.8
1202 oropharynx cancer 9.8
1203 megakaryocytic leukemia 9.8
1204 actinic keratosis 9.8
1205 pustular psoriasis 9.8
1206 subacute cerebellar degeneration 9.8
1207 sudden sensorineural hearing loss 9.8
1208 pacs1 syndrome 9.8
1209 cerebrofacial arteriovenous metameric syndrome 9.8
1210 rare tumor 9.8
1211 annular erythema 9.8
1212 seizures, benign familial neonatal, 1 9.8
1213 ventricular fibrillation, paroxysmal familial, 1 9.8
1214 huntington disease-like 3 9.8
1215 arthrogryposis, mental retardation, and seizures 9.8
1216 encephalopathy, progressive, early-onset, with episodic rhabdomyolysis 9.8
1217 inhalation anthrax 9.8
1218 peripheral artery disease 9.8
1219 renal fibrosis 9.8
1220 colorectal adenoma 9.8
1221 pain agnosia 9.8
1222 clostridium difficile colitis 9.8
1223 hypogonadotropic hypogonadism 9.8
1224 yaws 9.8
1225 pleural tuberculosis 9.8
1226 acute hemorrhagic conjunctivitis 9.8
1227 acromegaly 9.8
1228 central retinal vein occlusion 9.8
1229 auditory system disease 9.8
1230 parasitic protozoa infectious disease 9.8
1231 signet ring cell adenocarcinoma 9.8
1232 wheat allergy 9.8
1233 mutism 9.8
1234 microsporidiosis 9.8
1235 benign ependymoma 9.8
1236 cellular ependymoma 9.8
1237 molluscum contagiosum 9.8
1238 neurofibroma 9.8
1239 tenosynovitis 9.8
1240 upper respiratory tract disease 9.8
1241 genetic prion diseases 9.8
1242 autoimmune enteropathy 9.8
1243 bowen's disease 9.8
1244 hashimoto encephalopathy 9.8
1245 t-cell prolymphocytic leukemia 9.8
1246 cerebral atrophy 9.8
1247 isolated optic neuritis 9.8
1248 rare surgical neurologic disease 9.8
1249 severe immune-mediated enteropathy 9.8
1250 refractory anemia 9.8
1251 polyendocrinopathy 9.8
1252 lichen sclerosus et atrophicus 9.8
1253 chordoma 9.8
1254 kuru 9.8
1255 panbronchiolitis, diffuse 9.8
1256 pars planitis 9.8
1257 creatinine clearance quantitative trait locus 9.8
1258 fatty liver disease, nonalcoholic 1 9.8
1259 streptococcus pneumonia 9.8
1260 autoimmune glomerulonephritis 9.8
1261 aspiration pneumonia 9.8
1262 penicilliosis 9.8
1263 extrapulmonary tuberculosis 9.8
1264 acrodermatitis chronica atrophicans 9.8
1265 hyper ige syndrome 9.8
1266 pneumoconiosis 9.8
1267 anthracosis 9.8
1268 eosinophilic meningitis 9.8
1269 renal hypertension 9.8
1270 primary hyperparathyroidism 9.8
1271 branch retinal artery occlusion 9.8
1272 porphyria 9.8
1273 intestinal tuberculosis 9.8
1274 retinal vascular occlusion 9.8
1275 islet cell tumor 9.8
1276 hyperuricemia 9.8
1277 gestational choriocarcinoma 9.8
1278 syringoma 9.8
1279 west nile fever 9.8
1280 acinar cell carcinoma 9.8
1281 allergic contact dermatitis 9.8
1282 central nervous system lymphoma 9.8
1283 systemic mastocytosis 9.8
1284 rh isoimmunization 9.8
1285 prostate disease 9.8
1286 testicular yolk sac tumor 9.8
1287 hepatoblastoma 9.8
1288 retinal artery occlusion 9.8
1289 sezary's disease 9.8
1290 postpartum depression 9.8
1291 hydrocele 9.8
1292 leukoplakia 9.8
1293 sutton disease 2 9.8
1294 hypotonia 9.8
1295 meningitis and encephalitis 9.8
1296 syncope 9.8
1297 primary cutaneous b-cell lymphoma 9.8
1298 primary anetoderma 9.8
1299 neonatal alloimmune neutropenia 9.8
1300 thyroid tumor 9.8
1301 ige responsiveness, atopic 9.8
1302 pernicious anemia 9.8
1303 anemia, autoimmune hemolytic 9.8
1304 thymoma, familial 9.8
1305 gastric cancer 9.8
1306 deficiency anemia 9.8
1307 lymphocytic leukemia 9.8
1308 t cell deficiency 9.8
1309 candidiasis 9.8
1310 thymoma 9.8
1311 purpura 9.8
1312 hemolytic anemia 9.8
1313 transient hypogammaglobulinemia of infancy 9.8
1314 transient hypogammaglobulinemia 9.8
1315 chickenpox 9.8
1316 granulocytopenia 9.8
1317 graft-versus-host disease 9.7
1318 vitamin b12 deficiency 9.7
1319 alpha chain disease 9.7
1320 allergic hypersensitivity disease 9.7
1321 keratoconjunctivitis 9.7
1322 allergic encephalomyelitis 9.7
1323 dwarfism 9.7
1324 neurofibromatosis, type iv, of riccardi 9.7
1325 hemochromatosis, type 1 9.7
1326 moyamoya disease 1 9.7
1327 pituitary hormone deficiency, combined, 2 9.7
1328 hypophosphatemic rickets, x-linked recessive 9.7
1329 hypophosphatemic rickets, x-linked dominant 9.7
1330 oncocytoma 9.7
1331 retinitis pigmentosa 17 9.7
1332 patent ductus venosus 9.7
1333 alpha-thalassemia 9.7
1334 orthostatic intolerance 9.7
1335 severe cutaneous adverse reaction 9.7
1336 sydenham chorea 9.7
1337 distal arthrogryposis 9.7
1338 ovarian serous carcinoma 9.7
1339 ovarian clear cell carcinoma 9.7
1340 interleukin-7 receptor alpha deficiency 9.7
1341 cogan syndrome 9.7
1342 endometrial hyperplasia 9.7
1343 sparganosis 9.7
1344 pneumonic plague 9.7
1345 dirofilariasis 9.7
1346 esophageal varix 9.7
1347 corneal neovascularization 9.7
1348 bronchopneumonia 9.7
1349 neonatal thyrotoxicosis 9.7
1350 obstructive jaundice 9.7
1351 biliary atresia 9.7
1352 alcoholic liver cirrhosis 9.7
1353 gonadal dysgenesis 9.7
1354 impotence 9.7
1355 giant cell tumor 9.7
1356 drug-induced hepatitis 9.7
1357 myeloproliferative neoplasm 9.7
1358 keratopathy 9.7
1359 psychotic disorder 9.7
1360 germinoma 9.7
1361 lung benign neoplasm 9.7
1362 clear cell sarcoma 9.7
1363 pleomorphic adenoma 9.7
1364 lung oat cell carcinoma 9.7
1365 follicular adenoma 9.7
1366 actinomycosis 9.7
1367 subacute delirium 9.7
1368 pulmonary emphysema 9.7
1369 limb-girdle muscular dystrophy 9.7
1370 corticobasal degeneration 9.7
1371 lymphomatoid papulosis 9.7
1372 myxozoa 9.7
1373 recurrent respiratory papillomatosis 9.7
1374 superficial spreading melanoma 9.7
1375 drug-induced vasculitis 9.7
1376 erythema multiforme major 9.7
1377 lymphedema 9.7
1378 x-linked intellectual disability-macrocephaly-macroorchidism syndrome 9.7
1379 acute motor and sensory axonal neuropathy 9.7
1380 gastroesophageal reflux 9.7
1381 cardiac arrhythmia 9.7
1382 mastocytosis, cutaneous 9.7
1383 proline-negative auxotroph of hamster, complementation of 9.7
1384 lipoid congenital adrenal hyperplasia 9.7
1385 eosinophilic fasciitis 9.7
1386 nonarteritic anterior ischemic optic neuropathy 9.7
1387 body mass index quantitative trait locus 11 9.7
1388 renal cell carcinoma, papillary, 1 9.7
1389 scheie syndrome 9.7
1390 retinal cone dystrophy 4 9.7
1391 complement component 3 deficiency, autosomal recessive 9.7
1392 auditory neuropathy and optic atrophy 9.7
1393 splenic marginal zone lymphoma 9.7
1394 paraganglioma 9.7
1395 limb ischemia 9.7
1396 ileitis 9.7
1397 cow milk allergy 9.7
1398 erythema elevatum diutinum 9.7
1399 gastric lymphoma 9.7
1400 herpangina 9.7
1401 kyasanur forest disease 9.7
1402 choroiditis 9.7
1403 otosclerosis 9.7
1404 endemic goiter 9.7
1405 sick sinus syndrome 9.7
1406 urinary schistosomiasis 9.7
1407 interstitial cystitis 9.7
1408 cholecystitis 9.7
1409 essential thrombocythemia 9.7
1410 nocardiosis 9.7
1411 gallbladder cancer 9.7
1412 proctitis 9.7
1413 carotid artery thrombosis 9.7
1414 cervical adenocarcinoma 9.7
1415 pleural empyema 9.7
1416 lynch syndrome 9.7
1417 complement component 3 deficiency 9.7
1418 subcorneal pustular dermatosis 9.7
1419 duodenitis 9.7
1420 scotoma 9.7
1421 intrinsic asthma 9.7
1422 epiglottitis 9.7
1423 senile cataract 9.7
1424 autoimmune atrophic gastritis 9.7
1425 candida glabrata 9.7
1426 chromophil renal cell carcinoma 9.7
1427 fasting hypoglycemia 9.7
1428 mycetoma 9.7
1429 stevens-johnson syndrome/toxic epidermal necrolysis 9.7
1430 viral hemorrhagic fever 9.7
1431 hypersomnia 9.7
1432 idiopathic nephrotic syndrome 9.7
1433 secondary vasculitis 9.7
1434 pemphigus erythematosus 9.7
1435 exudative vitreoretinopathy 1 9.7
1436 fucosidase regulator 9.7
1437 myoclonus and ataxia 9.7
1438 porphyria cutanea tarda 9.7
1439 testicular torsion 9.7
1440 thrombocytopenia 2 9.7
1441 torticollis 9.7
1442 urate oxidase, pseudogene 9.7
1443 sudden infant death syndrome 9.7
1444 xeroderma pigmentosum, variant type 9.7
1445 rett syndrome 9.7
1446 body mass index quantitative trait locus 9 9.7
1447 body mass index quantitative trait locus 8 9.7
1448 maturity-onset diabetes of the young 9.7
1449 amyotrophic lateral sclerosis 3 9.7
1450 body mass index quantitative trait locus 4 9.7
1451 body mass index quantitative trait locus 10 9.7
1452 body mass index quantitative trait locus 7 9.7
1453 body mass index quantitative trait locus 12 9.7
1454 body mass index quantitative trait locus 14 9.7
1455 muscle hypertrophy 9.7
1456 leptin deficiency or dysfunction 9.7
1457 body mass index quantitative trait locus 18 9.7
1458 body mass index quantitative trait locus 19 9.7
1459 body mass index quantitative trait locus 20 9.7
1460 autoimmune cardiomyopathy 9.7
1461 primary cutaneous amyloidosis 9.7
1462 zollinger-ellison syndrome 9.7
1463 apraxia 9.7
1464 ischemic colitis 9.7
1465 collagenous colitis 9.7
1466 purpura fulminans 9.7
1467 hyperekplexia 9.7
1468 thymus lymphoma 9.7
1469 borderline leprosy 9.7
1470 viral pneumonia 9.7
1471 microcytic anemia 9.7
1472 plummer's disease 9.7
1473 oligohydramnios 9.7
1474 hereditary spherocytosis 9.7
1475 shipyard eye 9.7
1476 paronychia 9.7
1477 acute proliferative glomerulonephritis 9.7
1478 hyperinsulinemic hypoglycemia 9.7
1479 ichthyosis 9.7
1480 rectum adenocarcinoma 9.7
1481 macrocytic anemia 9.7
1482 gangliocytoma 9.7
1483 turner syndrome 9.7
1484 chronic wasting disease 9.7
1485 intracranial embolism 9.7
1486 folliculitis 9.7
1487 dysgerminoma 9.7
1488 endophthalmitis 9.7
1489 colorado tick fever 9.7
1490 schizoaffective disorder 9.7
1491 syringocystadenoma papilliferum 9.7
1492 uterine corpus serous adenocarcinoma 9.7
1493 diverticulitis 9.7
1494 seborrheic dermatitis 9.7
1495 pityriasis versicolor 9.7
1496 diabetic macular edema 9.7
1497 ulcerative stomatitis 9.7
1498 ankrd26-related thrombocytopenia 9.7
1499 autoimmune inner ear disease 9.7
1500 cutaneous sclerosis 9.7
1501 erythrokeratoderma ''en cocardes'' 9.7
1502 fibromatosis 9.7
1503 germ cells tumors 9.7
1504 nodular regenerative hyperplasia 9.7
1505 primary central nervous system lymphoma 9.7
1506 stachybotrys chartarum 9.7
1507 wallerian degeneration 9.7
1508 non-paraneoplastic limbic encephalitis 9.7
1509 transient congenital hypothyroidism 9.7
1510 virus-associated trichodysplasia spinulosa 9.7
1511 juvenile myasthenia gravis 9.7
1512 chronic relapsing inflammatory optic neuropathy 9.7
1513 pemphigus vegetans 9.7
1514 vitreoretinopathy 9.7
1515 ricin poisoning 9.7
1516 temporal arteritis 9.7
1517 cystic fibrosis 9.7
1518 omenn syndrome 9.7
1519 immunodeficiency 8 9.7
1520 vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome 9.7
1521 pulmonary hypertension 9.7
1522 inflammatory bowel disease 9.7
1523 good syndrome 9.7
1524 mastoiditis 9.7
1525 osteomyelitis 9.7
1526 tonsillitis 9.7
1527 suppurative otitis media 9.7
1528 dysgammaglobulinemia 9.7
1529 nephrotic syndrome 9.7
1530 thrombocytopenia due to platelet alloimmunization 9.7
1531 thrombocytopenia 9.7
1532 ectodermal dysplasia 9.7
1533 gastroenteritis 9.7
1534 dermatitis 9.7
1535 cellulitis 9.7
1536 gastric adenocarcinoma 9.7
1537 hepatitis e 9.7
1538 poliomyelitis 9.7
1539 bronchitis 9.7
1540 conjunctivitis 9.7
1541 b-cell lymphoma 9.7
1542 herpes simplex 9.7
1543 meningitis 9.7
1544 aphthous stomatitis 9.7
1545 alopecia 9.7
1546 growth hormone deficiency 9.7
1547 isolated agammaglobulinemia 9.7
1548 chlorpropamide-alcohol flushing 9.7
1549 keratosis, seborrheic 9.7
1550 tl antigen 9.7
1551 tobacco addiction 9.7
1552 vitreoretinopathy, neovascular inflammatory 9.7
1553 anencephaly 9.7
1554 chediak-higashi syndrome 9.7
1555 hemangiopericytoma, malignant 9.7
1556 arts syndrome 9.7
1557 mucopolysaccharidosis, type ii 9.7
1558 systemic lupus erythematosus 1 9.7
1559 malignant atrophic papulosis 9.7
1560 platelet glycoprotein iv deficiency 9.7
1561 rhabdoid tumor predisposition syndrome 1 9.7
1562 chilblain lupus 1 9.7
1563 c1q deficiency 9.7
1564 cyanosis, transient neonatal 9.7
1565 autoimmune lymphoproliferative syndrome, type v 9.7
1566 t-cell lymphoma, subcutaneous panniculitis-like 9.7
1567 hemophagocytic lymphohistiocytosis 9.7
1568 cryptogenic organizing pneumonia 9.7
1569 argentine hemorrhagic fever 9.7
1570 chorioamnionitis 9.7
1571 large cell neuroendocrine carcinoma 9.7
1572 mucosal melanoma 9.7
1573 withdrawal disorder 9.7
1574 microscopic colitis 9.7
1575 thyroid gland anaplastic carcinoma 9.7
1576 migraine with aura 9.7
1577 leukodystrophy 9.7
1578 premature menopause 9.7
1579 myiasis 9.7
1580 bartonellosis 9.7
1581 cauda equina syndrome 9.7
1582 gastroparesis 9.7
1583 hepatic coma 9.7
1584 neurosarcoidosis 9.7
1585 kwashiorkor 9.7
1586 patent foramen ovale 9.7
1587 multiple cranial nerve palsy 9.7
1588 pyuria 9.7
1589 niemann-pick disease 9.7
1590 chromoblastomycosis 9.7
1591 pineoblastoma 9.7
1592 vascular cancer 9.7
1593 mitral valve stenosis 9.7
1594 ankylosis 9.7
1595 glycogen storage disease 9.7
1596 cerebellar disease 9.7
1597 substance abuse 9.7
1598 bacterial vaginosis 9.7
1599 lactic acidosis 9.7
1600 rhabdoid cancer 9.7
1601 vaginal discharge 9.7
1602 granuloma annulare 9.7
1603 clear cell adenocarcinoma 9.7
1604 urinary tract obstruction 9.7
1605 chronic polyneuropathy 9.7
1606 blepharospasm 9.7
1607 eccrine acrospiroma 9.7
1608 spiradenoma 9.7
1609 cll/sll 9.7
1610 inverted follicular keratosis 9.7
1611 impetigo 9.7
1612 parasitic helminthiasis infectious disease 9.7
1613 achalasia 9.7
1614 diabetic neuropathy 9.7
1615 hypersensitivity vasculitis 9.7
1616 biliary tract cancer 9.7
1617 chronic thromboembolic pulmonary hypertension 9.7
1618 cluster headache 9.7
1619 cytomegalic inclusion disease 9.7
1620 enteropathy-associated t-cell lymphoma 9.7
1621 idiopathic neutropenia 9.7
1622 indolent b cell lymphoma 9.7
1623 lymphomatous thyroiditis 9.7
1624 melanoma-associated retinopathy 9.7
1625 spitz nevus 9.7
1626 staphylococcal toxic shock syndrome 9.7
1627 low-grade astrocytoma 9.7
1628 rare hereditary hemochromatosis 9.7
1629 scorpion envenomation 9.7
1630 malignant epithelial tumor of ovary 9.7
1631 staphylococcal scarlet fever 9.7
1632 large granular lymphocyte leukemia 9.7
1633 plasma cell tumor 9.7
1634 primary adrenal insufficiency 9.7
1635 streptococcal toxic-shock syndrome 9.7
1636 cd40 ligand deficiency 9.6 TNFRSF13C TNFRSF13B
1637 blood group, i system 9.6
1638 carcinoid tumors, intestinal 9.6
1639 coronary artery dissection, spontaneous 9.6
1640 hypercalcemia, infantile, 1 9.6
1641 lipomatosis, multiple 9.6
1642 amyotrophy, hereditary neuralgic 9.6
1643 exfoliation syndrome 9.6
1644 dowling-degos disease 1 9.6
1645 vesicoureteral reflux 1 9.6
1646 afibrinogenemia, congenital 9.6
1647 neuropathy, hereditary sensory and autonomic, type iii 9.6
1648 factor vii deficiency 9.6
1649 fanconi anemia, complementation group a 9.6
1650 hypoadrenocorticism, familial 9.6
1651 phenylketonuria 9.6
1652 tardive dyskinesia 9.6
1653 isolated growth hormone deficiency, type iii, with agammaglobulinemia 9.6
1654 thrombocytopenia 1 9.6
1655 acute insulin response 9.6
1656 alveolar soft part sarcoma 9.6
1657 huntington disease-like 2 9.6
1658 hypereosinophilic syndrome, idiopathic 9.6
1659 preterm premature rupture of the membranes 9.6
1660 pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis 9.6
1661 psoriasis 14, pustular 9.6
1662 barrett esophagus 9.6
1663 peripartum cardiomyopathy 9.6
1664 hypogonadotropic hypogonadism 10 with or without anosmia 9.6
1665 tatton-brown-rahman syndrome 9.6
1666 global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies 9.6
1667 chronic ulcer of skin 9.6
1668 livedoid vasculitis 9.6
1669 exanthema subitum 9.6
1670 endocervical adenocarcinoma 9.6
1671 brain glioma 9.6
1672 lymphocytic colitis 9.6
1673 atrial fibrillation 9.6
1674 inguinal hernia 9.6
1675 chronic myelomonocytic leukemia 9.6
1676 pleomorphic lipoma 9.6
1677 aortic atherosclerosis 9.6
1678 asbestosis 9.6
1679 breast cyst 9.6
1680 amyotrophic neuralgia 9.6
1681 fanconi syndrome 9.6
1682 acquired thrombocytopenia 9.6
1683 cardiac tamponade 9.6
1684 hyperandrogenism 9.6
1685 protein-energy malnutrition 9.6
1686 sympathetic ophthalmia 9.6
1687 vogt-koyanagi-harada disease 9.6
1688 spinal muscular atrophy 9.6
1689 trichuriasis 9.6
1690 central retinal artery occlusion 9.6
1691 nontoxic goiter 9.6
1692 exocrine pancreatic insufficiency 9.6
1693 hepatic encephalopathy 9.6
1694 osteopetrosis 9.6
1695 hepatic infarction 9.6
1696 necrotizing ulcerative gingivitis 9.6
1697 poems syndrome 9.6
1698 anus cancer 9.6
1699 adult dermatomyositis 9.6
1700 reye syndrome 9.6
1701 papilledema 9.6
1702 chronic cystitis 9.6
1703 bone cancer 9.6
1704 hidradenitis suppurativa 9.6
1705 hidradenitis 9.6
1706 polyclonal hypergammaglobulinemia 9.6
1707 hematologic cancer 9.6
1708 cystadenoma 9.6
1709 cystic teratoma 9.6
1710 skin atrophy 9.6
1711 long qt syndrome 9.6
1712 kidney cortex necrosis 9.6
1713 paratyphoid fever 9.6
1714 gliosarcoma 9.6
1715 gastrointestinal system cancer 9.6
1716 complex regional pain syndrome 9.6
1717 neurodermatitis 9.6
1718 cerebritis 9.6
1719 olfactory neuroblastoma 9.6
1720 cranial nerve palsy 9.6
1721 craniopharyngioma 9.6
1722 hidradenoma 9.6
1723 eosinophilic gastroenteritis 9.6
1724 akinetic mutism 9.6
1725 acneiform dermatitis 9.6
1726 persian gulf syndrome 9.6
1727 mucoepidermoid carcinoma 9.6
1728 ganglioneuroma 9.6
1729 adenocarcinoma in situ 9.6
1730 mixed glioma 9.6
1731 arteriosclerosis obliterans 9.6
1732 ureteral obstruction 9.6
1733 clear cell hidradenoma 9.6
1734 gastrinoma 9.6
1735 large intestine cancer 9.6
1736 ovarian serous cystadenocarcinoma 9.6
1737 inherited metabolic disorder 9.6
1738 juvenile pilocytic astrocytoma 9.6
1739 mitochondrial myopathy 9.6
1740 carotid artery occlusion 9.6
1741 mucormycosis 9.6
1742 night blindness 9.6
1743 perinatal necrotizing enterocolitis 9.6
1744 myeloid sarcoma 9.6
1745 pityriasis rosea 9.6
1746 learning disability 9.6
1747 rem sleep behavior disorder 9.6
1748 lymphangitis 9.6
1749 sarcocystosis 9.6
1750 lymph node disease 9.6
1751 eosinophilia-myalgia syndrome 9.6
1752 muscular dystrophy, duchenne and becker type 9.6
1753 trichorhinophalangeal syndrome 9.6
1754 acanthamoeba keratitis 9.6
1755 acute myeloblastic leukemia with maturation 9.6
1756 acute myeloblastic leukemia without maturation 9.6
1757 brittle diabetes 9.6
1758 chronic active epstein-barr virus infection 9.6
1759 chronic intestinal pseudoobstruction 9.6
1760 cramp-fasciculation syndrome 9.6
1761 cutaneous polyarteritis nodosa 9.6
1762 non-a-e hepatitis 9.6
1763 pythiosis 9.6
1764 retroperitoneal fibrosis 9.6
1765 stenotrophomonas maltophilia infection 9.6
1766 asbestos intoxication 9.6
1767 inflammatory myopathy with abundant macrophages 9.6
1768 rare hemorrhagic disorder 9.6
1769 paraneoplastic sensory ganglionopathy 9.6
1770 snakebite envenomation 9.6
1771 euthyroid graves orbitopathy 9.6
1772 homozygous familial hypercholesterolemia 9.6
1773 clear cell adenocarcinoma of the ovary 9.6
1774 premature aging 9.6
1775 infectious encephalitis 9.6
1776 cardiogenic shock 9.6
1777 hereditary optic neuropathy 9.6
1778 burkitt lymphoma 9.6
1779 kabuki syndrome 1 9.6
1780 keratitis, hereditary 9.6
1781 myositis 9.6
1782 leprosy 3 9.6
1783 lymphoid interstitial pneumonia 9.6
1784 proteasome-associated autoinflammatory syndrome 1 9.6
1785 ocular motor apraxia 9.6
1786 subacute sclerosing panencephalitis 9.6
1787 polycythemia vera 9.6
1788 immunodeficiency with hyper-igm, type 1 9.6
1789 gallbladder disease 1 9.6
1790 congenital hypothyroidism 9.6
1791 follicular lymphoma 9.6
1792 aphasia 9.6
1793 colitis 9.6
1794 stickler syndrome 9.6
1795 endometritis 9.6
1796 intracranial abscess 9.6
1797 rickets 9.6
1798 pertussis 9.6
1799 arteriovenous malformation 9.6
1800 pneumocystosis 9.6
1801 graves' disease 9.6
1802 locked-in syndrome 9.6
1803 quadriplegia 9.6
1804 keratoconjunctivitis sicca 9.6
1805 pure red-cell aplasia 9.6
1806 coccidioidomycosis 9.6
1807 cholestasis 9.6
1808 congenital hypogammaglobulinemia 9.6
1809 cryptosporidiosis 9.6
1810 epilepsy 9.6
1811 iron metabolism disease 9.6
1812 membranoproliferative glomerulonephritis 9.6
1813 granulomatous gastritis 9.6
1814 milk allergy 9.6
1815 hypersplenism 9.6
1816 hyperthyroidism 9.6
1817 polycythemia 9.6
1818 measles 9.6
1819 allergic asthma 9.6
1820 muscular dystrophy 9.6
1821 hypereosinophilic syndrome 9.6
1822 triple x syndrome 9.6
1823 hansen's disease 9.6
1824 lymphangiectasis 9.6
1825 meningococcemia 9.6
1826 neisseria meningitidis infection 9.6
1827 post-transplant lymphoproliferative disease 9.6
1828 vernal keratoconjunctivitis 9.6
1829 wandering spleen 9.6
1830 polyploidy 9.6
1831 red cell aplasia 9.6
1832 progressive familial heart block, type ia 9.6
1833 oculopharyngeal muscular dystrophy 9.6
1834 polycystic liver disease 1 with or without kidney cysts 9.6
1835 thyroid cancer, nonmedullary, 2 9.6
1836 factor xii deficiency 9.6
1837 multiple pterygium syndrome, lethal type 9.6
1838 fragile x syndrome 9.6
1839 meester-loeys syndrome 9.6
1840 fatal familial insomnia 9.6
1841 retinitis pigmentosa 11 9.6
1842 pituitary adenoma, prolactin-secreting 9.6
1843 convulsions, familial infantile, with paroxysmal choreoathetosis 9.6
1844 anorexia nervosa 9.6
1845 bone mineral density quantitative trait locus 3 9.6
1846 ovarian hyperstimulation syndrome 9.6
1847 asthma-related traits 2 9.6
1848 muscular dystrophy, congenital, lmna-related 9.6
1849 ectodermal dysplasia-syndactyly syndrome 2 9.6
1850 nestor-guillermo progeria syndrome 9.6
1851 human monocytic ehrlichiosis 9.6
1852 primary amebic meningoencephalitis 9.6
1853 hemorrhagic cystitis 9.6
1854 progressive familial intrahepatic cholestasis 9.6
1855 chronic meningitis 9.6
1856 chronic leukemia 9.6
1857 charcot-marie-tooth disease 9.6
1858 methemoglobinemia 9.6
1859 tooth disease 9.6
1860 intracranial aneurysm 9.6
1861 vitamin k deficiency bleeding 9.6
1862 brill-zinsser disease 9.6
1863 nephrosclerosis 9.6
1864 indeterminate leprosy 9.6
1865 paranoid schizophrenia 9.6
1866 secondary hyperparathyroidism 9.6
1867 transient global amnesia 9.6
1868 klebsiella pneumonia 9.6
1869 tuberous sclerosis 9.6
1870 pleural disease 9.6
1871 dermatomycosis 9.6
1872 pneumothorax 9.6
1873 factor xiii deficiency 9.6
1874 vulvovaginal candidiasis 9.6
1875 morphine dependence 9.6
1876 myoma 9.6
1877 laryngeal squamous cell carcinoma 9.6
1878 lobular neoplasia 9.6
1879 keratoacanthoma 9.6
1880 progressive muscular atrophy 9.6
1881 angiomyolipoma 9.6
1882 bone inflammation disease 9.6
1883 carotid artery disease 9.6
1884 mucinous cystadenocarcinoma 9.6
1885 ovarian cystadenocarcinoma 9.6
1886 acute retinal necrosis syndrome 9.6
1887 bladder disease 9.6
1888 intermittent claudication 9.6
1889 thyroid gland follicular carcinoma 9.6
1890 ganglioneuroblastoma 9.6
1891 endometrial stromal sarcoma 9.6
1892 polyradiculopathy 9.6
1893 marburg hemorrhagic fever 9.6
1894 lung large cell carcinoma 9.6
1895 hydranencephaly 9.6
1896 calciphylaxis 9.6
1897 sebaceous adenocarcinoma 9.6
1898 bronchiolo-alveolar adenocarcinoma 9.6
1899 tubular adenocarcinoma 9.6
1900 ganglioglioma 9.6
1901 arteriolosclerosis 9.6
1902 ovarian clear cell adenocarcinoma 9.6
1903 internuclear ophthalmoplegia 9.6
1904 mitral valve disease 9.6
1905 renal oncocytoma 9.6
1906 childhood leukemia 9.6
1907 osteochondrosis 9.6
1908 intestinal obstruction 9.6
1909 rheumatic myocarditis 9.6
1910 bullous skin disease 9.6
1911 parapsoriasis 9.6
1912 cleft lip 9.6
1913 renal tuberculosis 9.6
1914 drug dependence 9.6
1915 acquired pure red cell aplasia 9.6
1916 acute zonal occult outer retinopathy 9.6
1917 anaplastic oligodendroglioma 9.6
1918 bk-virus nephropathy 9.6
1919 bronchial adenomas/carcinoids childhood 9.6
1920 ciguatera fish poisoning 9.6
1921 congenital zika syndrome 9.6
1922 cutaneous mastocytoma 9.6
1923 eales disease 9.6
1924 embryonal sarcoma 9.6
1925 exercise-induced anaphylaxis 9.6
1926 hemorrhagic proctocolitis 9.6
1927 laryngeal papillomatosis 9.6
1928 mycobacterium marinum 9.6
1929 pediatric multiple sclerosis 9.6
1930 perniosis 9.6
1931 pustulosis palmaris et plantaris 9.6
1932 rosai-dorfman disease 9.6
1933 treponema infection 9.6
1934 febrile seizures 9.6
1935 t-cell non-hodgkin lymphoma 9.6
1936 progressive muscular dystrophy 9.6
1937 hemorrhagic fever-renal syndrome 9.6
1938 familial intrahepatic cholestasis 9.6
1939 refractory celiac disease 9.6
1940 osteonecrosis of the jaw 9.6
1941 acquired prothrombin deficiency 9.6
1942 autoimmune hypoparathyroidism 9.6
1943 acute adrenal insufficiency 9.6
1944 type ii mixed cryoglobulinemia 9.6
1945 spotted fever rickettsiosis 9.6
1946 amyloidosis, primary localized cutaneous, 1 9.5
1947 leukemia, chronic lymphocytic 2 9.5
1948 blood group, kidd system 9.5
1949 carpal tunnel syndrome 9.5
1950 cleft palate, isolated 9.5
1951 optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy 9.5
1952 fibromuscular dysplasia 9.5
1953 hemifacial atrophy, progressive 9.5
1954 hemifacial spasm, familial 9.5
1955 hypercalciuria, absorptive, 2 9.5
1956 intussusception 9.5
1957 paroxysmal extreme pain disorder 9.5
1958 pancreatitis, hereditary 9.5
1959 benign chronic pemphigus 9.5
1960 tuberous sclerosis 1 9.5
1961 congenital heart defects, hamartomas of tongue, and polysyndactyly 9.5
1962 factor v deficiency 9.5
1963 factor x deficiency 9.5
1964 friedreich ataxia 9.5
1965 galactorrhea 9.5
1966 autoimmune polyendocrine syndrome, type i, with or without reversible metaphyseal dysplasia 9.5
1967 lambert syndrome 9.5
1968 myoclonic epilepsy of lafora 9.5
1969 thrombotic thrombocytopenic purpura, congenital 9.5
1970 retinitis pigmentosa 24 9.5
1971 nystagmus 1, congenital, x-linked 9.5
1972 epilepsy, idiopathic generalized 9.5
1973 progressive familial heart block, type ib 9.5
1974 hypertension, early-onset, autosomal dominant, with severe exacerbation in pregnancy 9.5
1975 systemic lupus erythematosus 3 9.5
1976 diamond-blackfan anemia 2 9.5
1977 longevity 2 9.5
1978 lymphangioleiomyomatosis 9.5
1979 asthma-related traits 1 9.5
1980 migraine with or without aura 6 9.5
1981 anxiety 9.5
1982 neutrophilic dermatosis, acute febrile 9.5
1983 thrombocytopenia 4 9.5
1984 smoking as a quantitative trait locus 3 9.5
1985 systemic lupus erythematosus 14 9.5
1986 thrombocytopenia 6 9.5
1987 hypertrophic scars 9.5
1988 west syndrome 9.5
1989 autoimmune peripheral neuropathy 9.5
1990 pemphigus gestationis 9.5
1991 granulomatous amebic encephalitis 9.5
1992 infant botulism 9.5
1993 first-degree atrioventricular block 9.5
1994 second-degree atrioventricular block 9.5
1995 sinoatrial node disease 9.5
1996 sleep apnea 9.5
1997 adrenal cortical adenoma 9.5
1998 ameloblastoma 9.5
1999 heavy chain disease 9.5
2000 ileocolitis 9.5
2001 scoliosis 9.5
2002 adenoid hypertrophy 9.5
2003 fish allergy 9.5
2004 recessive dystrophic epidermolysis bullosa 9.5
2005 benign teratoma 9.5
2006 nodular malignant melanoma 9.5
2007 venous insufficiency 9.5
2008 hypopyon 9.5
2009 bubonic plague 9.5
2010 hydronephrosis 9.5
2011 anhidrosis 9.5
2012 megacolon 9.5
2013 denture stomatitis 9.5
2014 ischemic neuropathy 9.5
2015 pica disease 9.5
2016 neurogenic bladder 9.5
2017 low compliance bladder 9.5
2018 marasmus 9.5
2019 vulva cancer 9.5
2020 newborn respiratory distress syndrome 9.5
2021 cerebral atherosclerosis 9.5
2022 intermediate uveitis 9.5
2023 migraine without aura 9.5
2024 endomyocardial fibrosis 9.5
2025 tick-borne relapsing fever 9.5
2026 right bundle branch block 9.5
2027 oligospermia 9.5
2028 dracunculiasis 9.5
2029 lymphangioma 9.5
2030 personality disorder 9.5
2031 heart septal defect 9.5
2032 facial hemiatrophy 9.5
2033 peritoneal mesothelioma 9.5
2034 fallopian tube carcinoma 9.5
2035 exostosis 9.5
2036 hyperostosis 9.5
2037 intestinal perforation 9.5
2038 prothrombin deficiency 9.5
2039 granulomatous hepatitis 9.5
2040 craniosynostosis 9.5
2041 vernal conjunctivitis 9.5
2042 acalculous cholecystitis 9.5
2043 immune system disease 9.5
2044 hypersensitivity reaction type iv disease 9.5
2045 germ cell cancer 9.5
2046 skin squamous cell carcinoma 9.5
2047 spinal cord disease 9.5
2048 pancreatic ductal carcinoma 9.5
2049 empty sella syndrome 9.5
2050 anovulation 9.5
2051 hidrocystoma 9.5
2052 spindle cell carcinoma 9.5
2053 muscle cancer 9.5
2054 tricuspid valve insufficiency 9.5
2055 dyslexia 9.5
2056 diffuse glomerulonephritis 9.5
2057 apocrine adenocarcinoma 9.5
2058 alcoholic pancreatitis 9.5
2059 pleural cancer 9.5
2060 von economo's disease 9.5
2061 hemangioblastoma 9.5
2062 anterograde amnesia 9.5
2063 mature teratoma 9.5
2064 pediatric lymphoma 9.5
2065 eccrine porocarcinoma 9.5
2066 tertiary syphilis 9.5
2067 osteochondritis dissecans 9.5
2068 paralytic ileus 9.5
2069 polyhydramnios 9.5
2070 hypopharynx cancer 9.5
2071 rosacea 9.5
2072 autosomal dominant polycystic kidney disease 9.5
2073 hepatopulmonary syndrome 9.5
2074 hard palate cancer 9.5
2075 mast-cell leukemia 9.5
2076 priapism 9.5
2077 orbital disease 9.5
2078 croup 9.5
2079 staphyloenterotoxemia 9.5
2080 necrotizing fasciitis 9.5
2081 interstitial keratitis 9.5
2082 keloid disorder 9.5
2083 progressive myoclonus epilepsy, lafora type 9.5
2084 acquired angioedema 9.5
2085 aids dementia complex 9.5
2086 alopecia totalis 9.5
2087 anaplastic ependymoma 9.5
2088 banti's syndrome 9.5
2089 bone marrow necrosis 9.5
2090 chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids 9.5
2091 complement component deficiency 9.5
2092 congenital muscular dystrophy due to dystroglycanopathy 9.5
2093 coronary artery aneurysm 9.5
2094 cryofibrinogenemia 9.5
2095 dentinogenesis imperfecta type 2 9.5
2096 desmoplastic small round cell tumor 9.5
2097 hypocomplementemic urticarial vasculitis 9.5
2098 lentigo maligna melanoma 9.5
2099 monogenic diabetes 9.5
2100 neonatal meningitis 9.5
2101 neonatal stroke 9.5
2102 oligoastrocytoma 9.5
2103 oncogenic osteomalacia 9.5
2104 oral leukoplakia 9.5
2105 polymorphous low-grade adenocarcinoma 9.5
2106 reversible cerebral vasoconstriction syndrome 9.5
2107 testicular seminoma 9.5
2108 tièche-jadassohn nevus 9.5
2109 wells syndrome 9.5
2110 angiomatosis 9.5
2111 cerebral aneurysms 9.5
2112 hemifacial spasm 9.5
2113 spinocerebellar degeneration 9.5
2114 non-herpetic acute limbic encephalitis 9.5
2115 endotheliitis 9.5
2116 herpetiform pemphigus 9.5
2117 specific language disorder 9.5
2118 toxic oil syndrome 9.5
2119 qualitative or quantitative defects of alpha-dystroglycan 9.5
2120 idiopathic posterior uveitis 9.5
2121 transient neonatal myasthenia gravis 9.5
2122 recurrent idiopathic neuroretinitis 9.5
2123 paraquat poisoning 9.5
2124 lupus erythematosus panniculitis 9.5
2125 histiocytic sarcoma 9.5
2126 complement component 4, partial deficiency of 9.5
2127 hashimoto thyroiditis 9.5
2128 spondyloepiphyseal dysplasia with congenital joint dislocations 9.5
2129 attention deficit-hyperactivity disorder 9.5
2130 chromosome 18p deletion syndrome 9.5
2131 kaposi sarcoma 9.5
2132 systemic lupus erythematosus 9.5
2133 yellow nail syndrome 9.5
2134 cyclic neutropenia 9.5
2135 pulmonary hemosiderosis 9.5
2136 sarcoidosis 1 9.5
2137 smith-magenis syndrome 9.5
2138 thrombocytopenic purpura, autoimmune 9.5
2139 velocardiofacial syndrome 9.5
2140 vitiligo-associated multiple autoimmune disease susceptibility 6 9.5
2141 wolf-hirschhorn syndrome 9.5
2142 ataxia-telangiectasia 9.5
2143 autism 9.5
2144 celiac disease 1 9.5
2145 complement component 2 deficiency 9.5
2146 gaucher disease, type i 9.5
2147 lymphoma, hodgkin, classic 9.5
2148 familial mediterranean fever 9.5
2149 cartilage-hair hypoplasia 9.5
2150 microcephaly with chemotactic defect and transient hypogammaglobulinemia 9.5
2151 mulibrey nanism 9.5
2152 netherton syndrome 9.5
2153 pyle disease 9.5
2154 immunodeficiency 61 9.5
2155 severe combined immunodeficiency, x-linked 9.5
2156 wiskott-aldrich syndrome 9.5
2157 ectodermal dysplasia 1, hypohidrotic, x-linked 9.5
2158 premature ovarian failure 1 9.5
2159 ataxia and polyneuropathy, adult-onset 9.5
2160 severe combined immunodeficiency with sensitivity to ionizing radiation 9.5
2161 light fixation seizure syndrome 9.5
2162 wiedemann-steiner syndrome 9.5
2163 immunodeficiency with hyper-igm, type 2 9.5
2164 vitiligo-associated multiple autoimmune disease susceptibility 1 9.5
2165 body mass index quantitative trait locus 1 9.5
2166 pulmonary disease, chronic obstructive 9.5
2167 chromosome 16p13.3 deletion syndrome, proximal 9.5
2168 asthma-related traits 4 9.5
2169 breast-ovarian cancer, familial 2 9.5
2170 alpha-1-antitrypsin deficiency 9.5
2171 immunodeficiency 56 9.5
2172 immunodeficiency 12 9.5
2173 alacrima, achalasia, and mental retardation syndrome 9.5
2174 immunodeficiency 14 9.5
2175 immunodeficiency 13 9.5
2176 immunodeficiency 23 9.5
2177 ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus 9.5
2178 tick-borne encephalitis 9.5
2179 paralytic poliomyelitis 9.5
2180 autosomal recessive disease 9.5
2181 c1 inhibitor deficiency 9.5
2182 autism spectrum disorder 9.5
2183 lymphoma 9.5
2184 lung abscess 9.5
2185 respiratory allergy 9.5
2186 lymphoproliferative syndrome 9.5
2187 isolated growth hormone deficiency 9.5
2188 meningococcal meningitis 9.5
2189 sensorineural hearing loss 9.5
2190 dermatomyositis 9.5
2191 endocarditis 9.5
2192 protein-losing enteropathy 9.5
2193 portal hypertension 9.5
2194 hydrocephalus 9.5
2195 q fever 9.5
2196 sarcoma 9.5
2197 orbital cellulitis 9.5
2198 rabies 9.5
2199 chlamydia 9.5
2200 lyme disease 9.5
2201 visual epilepsy 9.5
2202 ecthyma 9.5
2203 hemosiderosis 9.5
2204 aseptic meningitis 9.5
2205 cough variant asthma 9.5
2206 leukemia 9.5
2207 telangiectasis 9.5
2208 guillain-barre syndrome 9.5
2209 uveitis 9.5
2210 acute cystitis 9.5
2211 megaloblastic anemia 9.5
2212 toxic shock syndrome 9.5
2213 chronic purulent otitis media 9.5
2214 oral candidiasis 9.5
2215 sclerosing cholangitis 9.5
2216 hypothyroidism 9.5
2217 aggressive periodontitis 9.5
2218 cystitis 9.5
2219 hepatitis c 9.5
2220 hypogonadism 9.5
2221 gaucher's disease 9.5
2222 leiomyosarcoma 9.5
2223 autoimmune hepatitis 9.5
2224 chronic mucocutaneous candidiasis 9.5
2225 dental caries 9.5
2226 epidermolysis bullosa 9.5
2227 cryoglobulinemia 9.5
2228 glomerulonephritis 9.5
2229 bronchiolitis 9.5
2230 anuria 9.5
2231 food allergy 9.5
2232 gingivitis 9.5
2233 thymic carcinoma 9.5
2234 skin carcinoma 9.5
2235 mixed connective tissue disease 9.5
2236 mastocytosis 9.5
2237 skin disease 9.5
2238 plasmacytoma 9.5
2239 systemic scleroderma 9.5
2240 spindle cell sarcoma 9.5
2241 pustulosis of palm and sole 9.5
2242 cervical adenitis 9.5
2243 central nervous system vasculitis 9.5
2244 intestinal disease 9.5
2245 pituitary gland disease 9.5
2246 complement deficiency 9.5
2247 acquired immunodeficiency syndrome 9.5
2248 connective tissue disease 9.5
2249 thyroiditis 9.5
2250 hypogonadotropism 9.5
2251 gastrointestinal system disease 9.5
2252 periodontitis 9.5
2253 fundus dystrophy 9.5
2254 herpes zoster 9.5
2255 ulcerative colitis 9.5
2256 myeloid leukemia 9.5
2257 crohn's disease 9.5
2258 rubella 9.5
2259 lupus erythematosus 9.5
2260 neuromyelitis optica 9.5
2261 psoriasis 9.5
2262 evans' syndrome 9.5
2263 diabetes mellitus 9.5
2264 cholangitis 9.5
2265 bacterial meningitis 9.5
2266 encephalitis 9.5
2267 alopecia areata 9.5
2268 18p deletion syndrome 9.5
2269 47,xyy 9.5
2270 sickle cell disease 9.5
2271 47, xxy 9.5
2272 anca-associated vasculitis 9.5
2273 bronchopulmonary dysplasia 9.5
2274 central congenital hypothyroidism 9.5
2275 chromosome 4p deletion 9.5
2276 congenital rubella 9.5
2277 guttate psoriasis 9.5
2278 tuberculous meningitis 9.5
2279 seizure disorder 9.5
2280 autoimmune hepatitis type 1 9.5
2281 inherited retinal disorder 9.5
2282 amyloidosis, hereditary, transthyretin-related 9.5
2283 cardiac conduction defect 9.5
2284 cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1 9.5
2285 maturity-onset diabetes of the young, type 2 9.5
2286 pilomatrixoma 9.5
2287 erythermalgia, primary 9.5
2288 gerstmann-straussler disease 9.5
2289 ichthyosis vulgaris 9.5
2290 facioscapulohumeral muscular dystrophy 1 9.5
2291 neurofibromatosis, type i 9.5
2292 ocular dominance 9.5
2293 spinocerebellar ataxia 1 9.5
2294 nephrolithiasis, calcium oxalate 9.5
2295 paragangliomas 1 9.5
2296 pityriasis rubra pilaris 9.5
2297 platelet groups--ko system 9.5
2298 polyposis, skin pigmentation, alopecia, and fingernail changes 9.5
2299 protoporphyria, erythropoietic, 1 9.5
2300 uterine anomalies 9.5
2301 vasculitis, lymphocytic, nodular 9.5
2302 abetalipoproteinemia 9.5
2303 acth deficiency, isolated 9.5
2304 alopecia universalis congenita 9.5
2305 leber congenital amaurosis 1 9.5
2306 arterial calcification, generalized, of infancy, 1 9.5
2307 macular dystrophy, corneal 9.5
2308 hypothyroidism, congenital, nongoitrous, 2 9.5
2309 schopf-schulz-passarge syndrome 9.5
2310 hyperlipoproteinemia, type i 9.5
2311 papillon-lefevre syndrome 9.5
2312 letterer-siwe disease 9.5
2313 metachromatic leukodystrophy 9.5
2314 mucopolysaccharidosis, type vi 9.5
2315 myopathy, congenital 9.5
2316 gitelman syndrome 9.5
2317 rhabdomyosarcoma 2 9.5
2318 senile plaque formation 9.5
2319 smith-lemli-opitz syndrome 9.5
2320 oliver-mcfarlane syndrome 9.5
2321 werner syndrome 9.5
2322 wilson disease 9.5
2323 xeroderma pigmentosum, complementation group a 9.5
2324 mcleod syndrome 9.5