AN
MCID: BLD137
MIFTS: 16

Blood Group--Ahonen (AN)

Categories: Blood diseases

Aliases & Classifications for Blood Group--Ahonen

MalaCards integrated aliases for Blood Group--Ahonen:

Name: Blood Group--Ahonen 56
an 56

Classifications:



External Ids:

OMIM 56 110350

Summaries for Blood Group--Ahonen

MalaCards based summary : Blood Group--Ahonen, also known as an, is related to hair-an syndrome and rare hemorrhagic disorder due to an acquired platelet anomaly. An important gene associated with Blood Group--Ahonen is AN (Blood Group Ahonen).

More information from OMIM: 110350

Related Diseases for Blood Group--Ahonen

Diseases related to Blood Group--Ahonen via text searches within MalaCards or GeneCards Suite gene sharing:

(showing 13217, show less)
# Related Disease Score Top Affiliating Genes
1 hair-an syndrome 12.4
2 rare hemorrhagic disorder due to an acquired platelet anomaly 12.3
3 hemophagocytic syndrome associated with an infection 12.2
4 rare hemorrhagic disorder due to an acquired coagulation factor defect 12.2
5 sickle cell disease associated with an other hemoglobin anomaly 12.2
6 silver-russell syndrome due to an imprinting defect of 11p15 12.2
7 hemolytic anemia due to an erythrocyte nucleotide metabolism disorder 12.2
8 sucking/swallowing disorder associated with an identified syndrome 12.1
9 rare thrombotic disorder due to an acquired platelet anomaly 12.1
10 rare thrombotic disorder due to an acquired coagulation factors defect 12.1
11 systemic inflammatory disease associated with an acquired peripheral neuropathy 12.1
12 hematological disease associated with an acquired peripheral neuropathy 12.1
13 solid tumor associated with an acquired peripheral neuropathy 12.1
14 rare female infertility due to an implantation defect 12.1
15 female infertility due to an implantation defect of genetic origin 12.1
16 rare female infertility due to an anomaly of ovarian function of genetic origin 12.1
17 rare female infertility due to an anomaly of ovarian function 12.1
18 rare female infertility due to an adrenal disorder 12.1
19 rare constitutional hemolytic anemia due to an enzyme disorder 12.1
20 congenital intestinal disease due to an enzymatic defect 12.1
21 alopecia, neurologic defects, and endocrinopathy syndrome 12.0
22 schizophrenia 11.8
23 aniridia 1 11.8
24 acanthosis nigricans 11.8
25 anorexia nervosa 11.7
26 acute necrotizing encephalitis 11.7
27 schizophrenia 1 11.6
28 schizophrenia 3 11.6
29 schizophrenia 7 11.6
30 polydactyly, preaxial iii 11.6
31 schizophrenia 18 11.6
32 encephalopathy, acute, infection-induced 4 11.5
33 schizophrenia 8 11.4
34 bile duct cystadenocarcinoma 11.4
35 schizophrenia 5 11.4
36 schizophrenia 9 11.4
37 systemic mastocytosis with associated hematologic neoplasm 11.4
38 schizophrenia 15 11.3
39 schizophrenia 19 11.3
40 aneurysm 11.2
41 diarrhea 11.1
42 migraine with or without aura 1 11.1
43 autoimmune disease 11.1
44 ataxia neuropathy spectrum 11.1
45 immunodeficiency due to a classical component pathway complement deficiency 11.1
46 aortic aneurysm 11.1
47 atrial fibrillation 11.1
48 down syndrome 11.1
49 stroke, ischemic 11.1
50 cardiac arrest 11.1
51 endocarditis 11.1
52 traumatic brain injury 11.1
53 hyperthyroidism 11.1
54 eating disorder 11.1
55 neuroblastoma 11.0
56 anxiety 11.0
57 encephalopathy 11.0
58 ovarian cancer 11.0
59 meningitis 11.0
60 systemic lupus erythematosus 11.0
61 47,xyy 11.0
62 cataract 11.0
63 breast cancer 11.0
64 aortic aneurysm, familial abdominal, 1 11.0
65 alcohol use disorder 11.0
66 cystic fibrosis 11.0
67 exanthem 11.0
68 respiratory failure 11.0
69 ocular motor apraxia 11.0
70 chronic pain 11.0
71 pulmonary embolism 11.0
72 adenoma 11.0
73 multiple sclerosis 11.0
74 hydrocephalus 11.0
75 pneumonia 11.0
76 head injury 11.0
77 immune deficiency disease 11.0
78 dilated cardiomyopathy 11.0
79 hemophilia 11.0
80 lyme disease 11.0
81 herpes simplex 11.0
82 beckwith-wiedemann syndrome 11.0
83 melanoma 11.0
84 vasculitis 11.0
85 disease of mental health 11.0
86 colorectal cancer 11.0
87 influenza 11.0
88 myocardial infarction 11.0
89 encephalitis 11.0
90 antiphospholipid syndrome 11.0
91 malaria 11.0
92 arteriovenous malformation 11.0
93 syncope 11.0
94 major depressive disorder 11.0
95 angina pectoris 11.0
96 multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly 11.0
97 kawasaki disease 11.0
98 pancreatic cancer 11.0
99 hypertension, essential 11.0
100 hepatitis a 11.0
101 huntington disease 11.0
102 aspergillosis 11.0
103 cholera 11.0
104 hepatitis c 11.0
105 lung cancer 11.0
106 obsessive-compulsive disorder 11.0
107 pulmonary disease, chronic obstructive 11.0
108 inflammatory bowel disease 11.0
109 vascular disease 11.0
110 rheumatoid arthritis 11.0
111 spinal cord injury 11.0
112 crohn's disease 11.0
113 asthma 11.0
114 back pain 11.0
115 dermatitis, atopic 11.0
116 diphtheria 11.0
117 kidney disease 11.0
118 retinoblastoma 11.0
119 chagas disease 11.0
120 alzheimer disease 11.0
121 polycythemia vera 11.0
122 esophagitis, eosinophilic, 1 11.0
123 osteomyelitis 11.0
124 osteoporosis 11.0
125 leukemia, chronic myeloid 10.9
126 familial adenomatous polyposis 10.9
127 peritonitis 10.9
128 leukemia, acute myeloid 10.9
129 graves' disease 10.9
130 pneumothorax, primary spontaneous 10.9
131 allergic hypersensitivity disease 10.9
132 myeloma, multiple 10.9
133 tremor 10.9
134 hepatitis b 10.9
135 osteoarthritis 10.9
136 aplastic anemia 10.9
137 celiac disease 1 10.9
138 measles 10.9
139 prostate cancer 10.9
140 bipolar disorder 10.9
141 fibrosis of extraocular muscles, congenital, 1 10.9
142 leishmaniasis 10.9
143 neural tube defects 10.9
144 brain injury 10.9
145 human immunodeficiency virus type 1 10.9
146 attention deficit-hyperactivity disorder 10.9
147 acute cystitis 10.9
148 phenylketonuria 10.9
149 hypertrophic cardiomyopathy 10.9
150 leukemia 10.9
151 depression 10.9
152 fabry disease 10.9
153 aging 10.9
154 gastric cancer 10.9
155 maple syrup urine disease 10.9
156 thalassemia 10.9
157 autism 10.9
158 porphyria 10.9
159 infective endocarditis 10.9
160 proteasome-associated autoinflammatory syndrome 1 10.9
161 retinal detachment 10.9
162 leukemia, acute lymphoblastic 10.9
163 chronic kidney disease 10.9
164 bladder cancer 10.9
165 osteogenic sarcoma 10.9
166 autism spectrum disorder 10.9
167 herpes zoster 10.9
168 xeroderma pigmentosum, variant type 10.9
169 barth syndrome 10.9
170 autoimmune lymphoproliferative syndrome 10.9
171 lysosomal acid lipase deficiency 10.9
172 helix syndrome 10.9
173 rabies 10.9
174 severe combined immunodeficiency 10.9
175 hypereosinophilic syndrome 10.9
176 seizure disorder 10.9
177 hyperlipoproteinemia, type iii 10.9
178 amyotrophic lateral sclerosis 1 10.9
179 pneumothorax 10.9
180 gastroenteritis 10.9
181 rapidly involuting congenital hemangioma 10.9
182 neutropenia 10.9
183 glioblastoma multiforme 10.9
184 ataxia-telangiectasia 10.9
185 hypoadrenocorticism, familial 10.9
186 acrocallosal syndrome 10.9
187 psoriasis 10.9
188 cleft palate, isolated 10.9
189 lupus erythematosus 10.9
190 atherosclerosis susceptibility 10.9
191 patent ductus arteriosus 1 10.9
192 beta-thalassemia 10.9
193 candidiasis 10.9
194 peptic ulcer disease 10.9
195 sarcoidosis 1 10.9
196 allergic rhinitis 10.9
197 dandy-walker syndrome 10.9
198 alcohol dependence 10.9
199 nevus, epidermal 10.9
200 septic arthritis 10.9
201 metachromatic leukodystrophy 10.9
202 headache 10.9
203 aicardi-goutieres syndrome 10.9
204 hyperparathyroidism 10.9
205 simpson-golabi-behmel syndrome 10.9
206 colitis 10.9
207 guillain-barre syndrome 10.9
208 chickenpox 10.9
209 allergic asthma 10.9
210 food allergy 10.9
211 polycystic ovary syndrome 10.9
212 achondroplasia 10.9
213 dementia 10.9
214 prion disease 10.9
215 body mass index quantitative trait locus 11 10.9
216 conjunctivitis 10.9
217 gastrointestinal ulceration, recurrent, with dysfunctional platelets 10.9
218 myopia 10.9
219 sleep apnea 10.9
220 lymphoma, hodgkin, classic 10.9
221 gastric cancer, hereditary diffuse 10.9
222 hepatocellular carcinoma 10.9
223 osteopetrosis 10.9
224 3-methylglutaconic aciduria, type iii 10.9
225 otitis media 10.9
226 infertility 10.9
227 hemochromatosis, type 1 10.9
228 peutz-jeghers syndrome 10.9
229 hashimoto thyroiditis 10.9
230 alpha-1-antitrypsin deficiency 10.9
231 cervical cancer 10.9
232 leptin deficiency or dysfunction 10.9
233 gout 10.9
234 abetalipoproteinemia 10.9
235 kaposi sarcoma 10.9
236 erythema multiforme 10.9
237 argininosuccinic aciduria 10.9
238 ventricular septal defect 10.9
239 myocarditis 10.9
240 homocystinuria 10.9
241 brugada syndrome 10.9
242 wolff-parkinson-white syndrome 10.9
243 arrhythmogenic right ventricular cardiomyopathy 10.9
244 tay-sachs disease 10.9
245 thrombosis 10.9
246 splenomegaly 10.9
247 arts syndrome 10.9
248 multiple acyl-coa dehydrogenase deficiency 10.9
249 pfeiffer syndrome 10.9
250 refsum disease, classic 10.9
251 neurofibromatosis, type ii 10.9
252 propionic acidemia 10.9
253 uveitis 10.9
254 adrenoleukodystrophy 10.9
255 myelofibrosis 10.9
256 rickets 10.9
257 spermatogenic failure 6 10.9
258 hansen's disease 10.9
259 alacrima, achalasia, and mental retardation syndrome 10.9
260 pain agnosia 10.9
261 niemann-pick disease 10.9
262 sandhoff disease 10.9
263 langerhans cell histiocytosis 10.9
264 marfan syndrome 10.9
265 avian influenza 10.9
266 nasopharyngeal carcinoma 10.9
267 restless legs syndrome 10.9
268 glutaric acidemia i 10.9
269 anemia, x-linked, with or without neutropenia and/or platelet abnormalities 10.9
270 inguinal hernia 10.9
271 fatty liver disease 10.9
272 glycogen storage disease ii 10.9
273 macular degeneration, age-related, 1 10.9
274 neurofibromatosis, type i 10.9
275 alkaptonuria 10.9
276 myasthenia gravis 10.9
277 epilepsy 10.9
278 exstrophy of bladder 10.9
279 gaucher disease, type i 10.9
280 hypothyroidism 10.9
281 hemophilia a 10.9
282 myotonic dystrophy 10.9
283 optic atrophy 1 10.9
284 intracranial aneurysm 10.9
285 hemophilia b 10.9
286 pendred syndrome 10.9
287 galactosemia i 10.9
288 systemic scleroderma 10.9
289 familial mediterranean fever 10.9
290 renal cell carcinoma, nonpapillary 10.9
291 wiskott-aldrich syndrome 10.9
292 neuromyelitis optica 10.9
293 bronchitis 10.9
294 goiter 10.9
295 narcolepsy 10.9
296 yemenite deaf-blind hypopigmentation syndrome 10.9
297 intraocular pressure quantitative trait locus 10.9
298 dengue disease 10.9
299 diffuse large b-cell lymphoma 10.9
300 iron metabolism disease 10.9
301 helicobacter pylori infection 10.9
302 ulcerative colitis 10.9
303 patent foramen ovale 10.9
304 friedreich ataxia 10.9
305 hypogonadotropic hypogonadism 10.9
306 abdominal wall defect 10.9
307 von willebrand's disease 10.9
308 pertussis 10.9
309 ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus 10.9
310 thrombophilia due to thrombin defect 10.9
311 rubella 10.9
312 farber lipogranulomatosis 10.9
313 anthrax disease 10.9
314 parkinson disease, late-onset 10.9
315 vitiligo-associated multiple autoimmune disease susceptibility 1 10.9
316 cleft lip 10.9
317 bulimia nervosa 10.9
318 cellulitis 10.9
319 wilson disease 10.9
320 deficiency anemia 10.9
321 darier-white disease 10.9
322 graft-versus-host disease 10.9
323 paroxysmal nocturnal hemoglobinuria 10.9
324 diarrhea 5, with tufting enteropathy, congenital 10.9
325 antithrombin iii deficiency 10.9
326 craniosynostosis 10.9
327 lynch syndrome 10.9
328 ovarian cyst 10.9
329 alpha/beta t-cell lymphopenia with gamma/delta t-cell expansion, severe cytomegalovirus infection, and autoimmunity 10.9
330 teratoma 10.9
331 holt-oram syndrome 10.9
332 pulmonary hypertension 10.9
333 reactive arthritis 10.9
334 gm1 gangliosidosis 10.9
335 diabetes mellitus, ketosis-prone 10.9
336 stiff-person syndrome 10.8
337 cardiomyopathy, familial hypertrophic, 1 10.8
338 neuropathy, hereditary, with liability to pressure palsies 10.8
339 sudden infant death syndrome 10.8
340 barrett esophagus 10.8
341 coronary heart disease 1 10.8
342 aortic dissection 10.8
343 catecholaminergic polymorphic ventricular tachycardia 10.8
344 cartilage-hair hypoplasia 10.8
345 poliomyelitis 10.8
346 isovaleric acidemia 10.8
347 hyperglycemia 10.8
348 hyperlysinemia, type i 10.8
349 hyperkalemic periodic paralysis 10.8
350 panic disorder 10.8
351 pemphigus 10.8
352 cowden syndrome 10.8
353 loeys-dietz syndrome 10.8
354 congenital generalized lipodystrophy 10.8
355 long qt syndrome 10.8
356 tangier disease 10.8
357 carnitine palmitoyltransferase ii deficiency, infantile 10.8
358 hemophagocytic lymphohistiocytosis, familial, 1 10.8
359 tetanus 10.8
360 lipoprotein quantitative trait locus 10.8
361 menkes disease 10.8
362 congenital hemidysplasia with ichthyosiform erythroderma and limb defects 10.8
363 pelizaeus-merzbacher disease 10.8
364 pericardial effusion 10.8
365 lateral sclerosis 10.8
366 exudative vitreoretinopathy 1 10.8
367 sjogren syndrome 10.8
368 sotos syndrome 1 10.8
369 chylomicron retention disease 10.8
370 diabetes mellitus 10.8
371 lichen planus 10.8
372 rhabdomyosarcoma 10.8
373 acute pancreatitis 10.8
374 moyamoya disease 1 10.8
375 arthritis 10.8
376 familial partial lipodystrophy 10.8
377 thrombocytopenic purpura, autoimmune 10.8
378 skin disease 10.8
379 diaphragmatic hernia, congenital 10.8
380 toxoplasmosis 10.8
381 acute kidney failure 10.8
382 west syndrome 10.8
383 aphasia 10.8
384 supranuclear palsy, progressive, 1 10.8
385 pre-eclampsia 10.8
386 dehydrated hereditary stomatocytosis 1 with or without pseudohyperkalemia and/or perinatal edema 10.8
387 lipid metabolism disorder 10.8
388 charge syndrome 10.8
389 smith-lemli-opitz syndrome 10.8
390 endometriosis 10.8
391 amyloidosis 10.8
392 myopathy 10.8
393 alexander disease 10.8
394 anemia, sideroblastic, 1 10.8
395 fibromyalgia 10.8
396 eye disease 10.8
397 thrombocytopenia due to platelet alloimmunization 10.8
398 pulmonary hypertension, primary, 1 10.8
399 mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome 10.8
400 adenine phosphoribosyltransferase deficiency 10.8
401 microcephaly 10.8
402 aicardi-goutieres syndrome 1 10.8
403 familial woolly hair syndrome 10.8
404 hemosiderosis 10.8
405 leprosy 3 10.8
406 glomerulonephritis 10.8
407 neurofibromatosis 10.8
408 insulin-like growth factor i 10.8
409 chronic granulomatous disease 10.8
410 cerebrovascular disease 10.8
411 aspartylglucosaminuria 10.8
412 vaginitis 10.8
413 danon disease 10.8
414 ventricular fibrillation, paroxysmal familial, 1 10.8
415 arteries, anomalies of 10.8
416 three m syndrome 1 10.8
417 phosphoribosylpyrophosphate synthetase superactivity 10.8
418 lymphangioleiomyomatosis 10.8
419 juvenile polyposis syndrome 10.8
420 kearns-sayre syndrome 10.8
421 cystinuria 10.8
422 bullous pemphigoid 10.8
423 cholangitis, primary sclerosing 10.8
424 machado-joseph disease 10.8
425 bone resorption disease 10.8
426 behcet syndrome 10.8
427 igg4-related disease 10.8
428 hypercholesterolemia, familial, 1 10.8
429 ovarian hyperstimulation syndrome 10.8
430 paresthesia 10.8
431 asperger syndrome 10.8
432 bloom syndrome 10.8
433 3-methylcrotonyl-coa carboxylase deficiency 10.8
434 intestinal obstruction 10.8
435 crouzon syndrome 10.8
436 aicardi syndrome 10.8
437 progressive familial heart block, type ia 10.8
438 von hippel-lindau syndrome 10.8
439 psoriatic arthritis 10.8
440 cowden syndrome 1 10.8
441 mevalonic aciduria 10.8
442 li-fraumeni syndrome 10.8
443 cystinosis 10.8
444 pulmonary tuberculosis 10.8
445 oral cancer 10.8
446 3-hydroxy-3-methylglutaryl-coa lyase deficiency 10.8
447 familial hemiplegic migraine 10.8
448 mesothelioma, malignant 10.8
449 keratitis, hereditary 10.8
450 acute promyelocytic leukemia 10.8
451 hypophosphatasia 10.8
452 post-traumatic stress disorder 10.8
453 glycogen storage disease iii 10.8
454 glycogen storage disease vii 10.8
455 cerebral creatine deficiency syndrome 2 10.8
456 albinism, oculocutaneous, type ii 10.8
457 impotence 10.8
458 carpal tunnel syndrome 10.8
459 galactosialidosis 10.8
460 chromosomal triplication 10.8
461 metabolic acidosis 10.8
462 ehlers-danlos syndrome 10.8
463 sturge-weber syndrome 10.8
464 fructose intolerance, hereditary 10.8
465 familial cold autoinflammatory syndrome 10.8
466 larsen syndrome 10.8
467 galactosemia ii 10.8
468 acatalasemia 10.8
469 atrial heart septal defect 10.8
470 diabetes mellitus, noninsulin-dependent 10.8
471 greig cephalopolysyndactyly syndrome 10.8
472 adrenal hypoplasia, congenital 10.8
473 congenital dyserythropoietic anemia 10.8
474 amyloidosis, hereditary, transthyretin-related 10.8
475 scoliosis 10.8
476 pseudoachondroplasia 10.8
477 krabbe disease 10.8
478 gestational diabetes 10.8
479 desmoid tumor 10.8
480 pneumocystosis 10.8
481 generalized anxiety disorder 10.8
482 focal dermal hypoplasia 10.8
483 coproporphyria, hereditary 10.8
484 megalencephalic leukoencephalopathy with subcortical cysts 1 10.8
485 scleroderma, familial progressive 10.8
486 carney complex variant 10.8
487 skin carcinoma 10.8
488 acromegaly 10.8
489 babesiosis 10.8
490 duodenal atresia 10.8
491 esophageal cancer 10.8
492 optic nerve disease 10.8
493 campomelic dysplasia 10.8
494 sleeping sickness 10.8
495 brittle bone disorder 10.8
496 cat-scratch disease 10.8
497 wilms tumor 1 10.8
498 hairy cell leukemia 10.8
499 noonan syndrome 1 10.8
500 syndromic x-linked intellectual disability snyder type 10.8
501 blepharophimosis, ptosis, and epicanthus inversus 10.8
502 sjogren-larsson syndrome 10.8
503 systemic onset juvenile idiopathic arthritis 10.8
504 peripheral nervous system disease 10.8
505 muscular dystrophy 10.8
506 meningioma, radiation-induced 10.8
507 onchocerciasis 10.8
508 irritable bowel syndrome 10.8
509 malignant fibrous histiocytoma 10.8
510 chikungunya 10.8
511 lymphopenia 10.8
512 spondyloepiphyseal dysplasia congenita 10.8
513 alpha-methylacetoacetic aciduria 10.8
514 basal ganglia calcification, idiopathic, 1 10.8
515 pseudoxanthoma elasticum 10.8
516 cerebral palsy 10.8
517 pleural empyema 10.8
518 homocysteinemia 10.8
519 mismatch repair cancer syndrome 10.8
520 fainting 10.8
521 stenotrophomonas maltophilia infection 10.8
522 atrioventricular block 10.8
523 citrullinemia, classic 10.8
524 tonsillitis 10.8
525 familial hypercholesterolemia 10.8
526 acyl-coa dehydrogenase, very long-chain, deficiency of 10.8
527 dwarfism 10.8
528 exophthalmos 10.8
529 spasticity 10.8
530 disseminated intravascular coagulation 10.8
531 papilloma 10.8
532 autonomic dysfunction 10.8
533 meningoencephalitis 10.8
534 agnosia 10.8
535 ellis-van creveld syndrome 10.8
536 congenital myasthenic syndrome 10.8
537 camurati-engelmann disease 10.8
538 congenital disorder of glycosylation, type ia 10.8
539 pyruvate carboxylase deficiency 10.8
540 opitz-kaveggia syndrome 10.8
541 myositis 10.8
542 psychotic disorder 10.8
543 small cell cancer of the lung 10.8
544 pyruvate kinase deficiency of red cells 10.8
545 triple x syndrome 10.8
546 chromosome 2q35 duplication syndrome 10.8
547 primary biliary cirrhosis 10.8
548 homocystinuria due to cystathionine beta-synthase deficiency 10.8
549 plague 10.8
550 heparin-induced thrombocytopenia 10.8
551 common variable immunodeficiency 10.8
552 haemophilus influenzae 10.8
553 cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1 10.8
554 leigh syndrome 10.8
555 breast-ovarian cancer, familial 2 10.8
556 methylmalonic acidemia 10.8
557 diamond-blackfan anemia 10.8
558 van buchem disease 10.8
559 schindler disease 10.8
560 heterotaxy 10.8
561 gitelman syndrome 10.8
562 gastritis 10.8
563 juvenile rheumatoid arthritis 10.8
564 cerebral aneurysms 10.8
565 short qt syndrome 10.8
566 dengue virus 10.8
567 polycystic kidney disease 10.8
568 neurodegeneration with brain iron accumulation 10.8
569 in situ carcinoma 10.8
570 medulloblastoma 10.8
571 sucrase-isomaltase deficiency, congenital 10.8
572 peters-plus syndrome 10.8
573 scoliosis, isolated 1 10.8
574 shigellosis 10.8
575 lymphedema-distichiasis syndrome 10.8
576 deafness, onychodystrophy, osteodystrophy, mental retardation, and seizures syndrome 10.8
577 duane-radial ray syndrome 10.8
578 canavan disease 10.8
579 hyperuricemia 10.8
580 seborrheic dermatitis 10.8
581 hernia, hiatus 10.8
582 anemia, autoimmune hemolytic 10.8
583 pancreas disease 10.8
584 caffey disease 10.8
585 biotinidase deficiency 10.8
586 mucopolysaccharidosis, type ii 10.8
587 aseptic meningitis 10.8
588 hyperferritinemia with or without cataract 10.8
589 48,xxyy syndrome 10.8
590 fragile x syndrome 10.8
591 thrombophilia 10.8
592 mycobacterium tuberculosis 1 10.8
593 periodic fever, familial, autosomal dominant 10.8
594 laron syndrome 10.8
595 fanconi anemia, complementation group a 10.8
596 protoporphyria, erythropoietic, 1 10.8
597 glucosephosphate dehydrogenase deficiency 10.8
598 mucolipidosis iv 10.8
599 niemann-pick disease, type a 10.8
600 alagille syndrome 1 10.8
601 microphthalmia 10.8
602 hypospadias 10.8
603 pentosuria 10.8
604 sarcosinemia 10.8
605 mohr-tranebjaerg syndrome 10.8
606 mosaic variegated aneuploidy syndrome 10.8
607 visceral leishmaniasis 10.8
608 follicular lymphoma 10.8
609 central core disease of muscle 10.8
610 coumarin resistance 10.8
611 trichothiodystrophy 10.8
612 endophthalmitis 10.8
613 lambert-eaton myasthenic syndrome 10.8
614 hemolytic anemia 10.8
615 limb-girdle muscular dystrophy 10.8
616 autosomal dominant nocturnal frontal lobe epilepsy 10.8
617 paraplegia 10.8
618 melioidosis 10.8
619 mumps 10.8
620 cholecystitis 10.8
621 joubert syndrome 1 10.8
622 androgen insensitivity, partial 10.8
623 stargardt disease 10.8
624 brucellosis 10.8
625 arthrogryposis, distal, type 2a 10.8
626 argininemia 10.8
627 mucopolysaccharidosis, type vi 10.8
628 lymphoproliferative syndrome, x-linked, 1 10.8
629 inflammatory myofibroblastic tumor 10.8
630 tricuspid atresia 10.8
631 hypokalemic periodic paralysis, type 1 10.8
632 rheumatic fever 10.8
633 creutzfeldt-jakob disease 10.8
634 diastrophic dysplasia 10.8
635 glycogen storage disease iv 10.8
636 neurodegeneration with brain iron accumulation 1 10.8
637 pallister-killian syndrome 10.8
638 systemic mastocytosis 10.8
639 focal epilepsy 10.8
640 complex regional pain syndrome 10.8
641 connective tissue disease 10.8
642 megaloblastic anemia 10.8
643 rett syndrome 10.8
644 pheochromocytoma 10.8
645 portal hypertension 10.8
646 cryptosporidiosis 10.8
647 cholangitis 10.8
648 transient cerebral ischemia 10.8
649 zika fever 10.8
650 learning disability 10.8
651 spondylitis 10.8
652 albinism, oculocutaneous, type ia 10.8
653 papillon-lefevre syndrome 10.8
654 spinal and bulbar muscular atrophy, x-linked 1 10.8
655 vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome 10.8
656 androgen insensitivity syndrome 10.8
657 frontotemporal dementia 10.8
658 lung cancer susceptibility 3 10.8
659 schizoaffective disorder 10.8
660 myelodysplastic syndrome 10.8
661 treacher collins syndrome 1 10.8
662 pancreatitis, hereditary 10.8
663 brachydactyly 10.8
664 weill-marchesani syndrome 10.8
665 opitz-gbbb syndrome 10.8
666 factor v leiden thrombophilia 10.8
667 harlequin syndrome 10.8
668 movement disease 10.8
669 hypochondriasis 10.8
670 kleine-levin hibernation syndrome 10.8
671 cerebrotendinous xanthomatosis 10.8
672 lipomatosis, multiple 10.8
673 allergic contact dermatitis 10.8
674 scabies 10.8
675 breast-ovarian cancer, familial 1 10.8
676 familial cold autoinflammatory syndrome 3 10.8
677 amblyopia 10.8
678 enthesopathy 10.8
679 central hypoventilation syndrome, congenital 10.8
680 glanzmann thrombasthenia 10.8
681 non-alcoholic fatty liver disease 10.8
682 cyclic vomiting syndrome 10.8
683 tuberous sclerosis 1 10.8
684 myopathy, tubular aggregate, 1 10.8
685 granulomatosis with polyangiitis 10.8
686 bacterial meningitis 10.8
687 adrenal cortical carcinoma 10.8
688 pulmonary fibrosis 10.8
689 hepatitis 10.8
690 esophageal atresia 10.8
691 restrictive cardiomyopathy 10.8
692 primary ciliary dyskinesia 10.8
693 bowen-conradi syndrome 10.8
694 holocarboxylase synthetase deficiency 10.8
695 neu-laxova syndrome 1 10.8
696 pseudovaginal perineoscrotal hypospadias 10.8
697 tn polyagglutination syndrome 10.8
698 fumarase deficiency 10.8
699 lathosterolosis 10.8
700 acquired generalized lipodystrophy 10.8
701 familial lipoprotein lipase deficiency 10.8
702 free sialic acid storage disorders 10.8
703 mitochondrial membrane protein-associated neurodegeneration 10.8
704 methylmalonic acidemia with homocystinuria 10.8
705 pure autonomic failure 10.8
706 aldosterone-producing adenoma 10.8
707 extrinsic allergic alveolitis 10.8
708 neurodegeneration with brain iron accumulation 2a 10.8
709 choroideremia 10.8
710 acute stress disorder 10.8
711 interstitial lung disease 10.8
712 cholestasis 10.8
713 essential thrombocythemia 10.8
714 spinal muscular atrophy 10.8
715 ornithine transcarbamylase deficiency, hyperammonemia due to 10.8
716 hyperekplexia 10.8
717 legionnaire disease 10.8
718 hemophagocytic lymphohistiocytosis 10.8
719 otodental dysplasia 10.8
720 spondyloepimetaphyseal dysplasia, strudwick type 10.8
721 fraser syndrome 1 10.8
722 donnai-barrow syndrome 10.8
723 fructose-1,6-bisphosphatase deficiency 10.8
724 volvulus of midgut 10.8
725 usher syndrome 10.8
726 protein s deficiency 10.8
727 acth-secreting pituitary adenoma 10.8
728 hypertelorism 10.8
729 primary central nervous system lymphoma 10.8
730 pelvic inflammatory disease 10.8
731 neuroretinitis 10.8
732 cerebral amyloid angiopathy, cst3-related 10.8
733 pulmonary edema 10.8
734 omenn syndrome 10.8
735 axenfeld-rieger syndrome 10.8
736 hereditary elliptocytosis 10.8
737 pericarditis 10.8
738 histiocytosis 10.8
739 agammaglobulinemia, x-linked 10.8
740 erdheim-chester disease 10.8
741 apraxia 10.8
742 dowling-degos disease 1 10.8
743 neuropathy, hereditary sensory and autonomic, type iii 10.8
744 mucopolysaccharidosis, type vii 10.8
745 aceruloplasminemia 10.8
746 microcephalic osteodysplastic primordial dwarfism, type ii 10.8
747 desbuquois dysplasia 1 10.8
748 d-bifunctional protein deficiency 10.8
749 mitochondrial dna depletion syndrome 7 10.8
750 hennekam syndrome 10.8
751 typhoid fever 10.8
752 sleep disorder 10.7
753 macroglossia 10.7
754 congenital hydrocephalus 10.7
755 myotonic dystrophy 1 10.7
756 andersen cardiodysrhythmic periodic paralysis 10.7
757 dihydropyrimidine dehydrogenase deficiency 10.7
758 cysticercosis 10.7
759 rothmund-thomson syndrome, type 2 10.7
760 hutchinson-gilford progeria syndrome 10.7
761 endogenous depression 10.7
762 enterocolitis 10.7
763 hypoxia 10.7
764 blau syndrome 10.7
765 lysinuric protein intolerance 10.7
766 acromicric dysplasia 10.7
767 erythrocytosis, familial, 1 10.7
768 corticosterone methyloxidase type i deficiency 10.7
769 perlman syndrome 10.7
770 epilepsy, familial focal, with variable foci 1 10.7
771 albinism, oculocutaneous, type ib 10.7
772 2-methylbutyryl-coa dehydrogenase deficiency 10.7
773 aortic valve disease 1 10.7
774 peripheral artery disease 10.7
775 myoclonic epilepsy of lafora 10.7
776 tyrosinemia, type i 10.7
777 waldenstroem's macroglobulinemia 10.7
778 paroxysmal cold hemoglobinuria 10.7
779 epidermodysplasia verruciformis 1 10.7
780 pemphigus vulgaris, familial 10.7
781 cleidocranial dysplasia 10.7
782 fibrodysplasia ossificans progressiva 10.7
783 cohen syndrome 10.7
784 glycogen storage disease ia 10.7
785 gyrate atrophy of choroid and retina 10.7
786 griscelli syndrome 10.7
787 muscular dystrophy, duchenne type 10.7
788 anencephaly 10.7
789 mucopolysaccharidosis-plus syndrome 10.7
790 nonarteritic anterior ischemic optic neuropathy 10.7
791 nephronophthisis 10.7
792 vitreoretinopathy, neovascular inflammatory 10.7
793 williams-beuren syndrome 10.7
794 saethre-chotzen syndrome 10.7
795 leukodystrophy 10.7
796 biliary atresia 10.7
797 ebola hemorrhagic fever 10.7
798 leber plus disease 10.7
799 astigmatism 10.7
800 chlamydia pneumonia 10.7
801 west nile virus 10.7
802 sickle cell disease 10.7
803 strabismus 10.7
804 frontonasal dysplasia 1 10.7
805 glycogen storage disease v 10.7
806 factor xii deficiency 10.7
807 aromatic l-amino acid decarboxylase deficiency 10.7
808 fatty liver disease, nonalcoholic 1 10.7
809 dysautonomia 10.7
810 apnea, obstructive sleep 10.7
811 nocardiosis 10.7
812 prostatic hyperplasia, benign 10.7
813 ectopic pregnancy 10.7
814 prader-willi syndrome 10.7
815 glycoproteinosis 10.7
816 temporal arteritis 10.7
817 niemann-pick disease, type c1 10.7
818 hereditary spherocytosis 10.7
819 proteus syndrome 10.7
820 netherton syndrome 10.7
821 factor xi deficiency 10.7
822 adenylosuccinase deficiency 10.7
823 popliteal pterygium syndrome 10.7
824 episodic kinesigenic dyskinesia 1 10.7
825 liddle syndrome 1 10.7
826 mucopolysaccharidosis, type iiib 10.7
827 autosomal recessive disease 10.7
828 japanese encephalitis 10.7
829 glycogen storage disease 10.7
830 alveolar soft part sarcoma 10.7
831 common cold 10.7
832 isolated ectopia lentis 10.7
833 western equine encephalitis 10.7
834 gray platelet syndrome 10.7
835 mowat-wilson syndrome 10.7
836 aarskog-scott syndrome 10.7
837 encephalopathy, ethylmalonic 10.7
838 allergic bronchopulmonary aspergillosis 10.7
839 oral candidiasis 10.7
840 ptosis 10.7
841 dentatorubral-pallidoluysian atrophy 10.7
842 mend syndrome 10.7
843 cholangiocarcinoma 10.7
844 hyperinsulinism 10.7
845 paget's disease of bone 10.7
846 ichthyosis vulgaris 10.7
847 eastern equine encephalitis 10.7
848 hyper-ige recurrent infection syndrome 1, autosomal dominant 10.7
849 macular dystrophy, corneal 10.7
850 gm1-gangliosidosis, type i 10.7
851 vici syndrome 10.7
852 schimke immunoosseous dysplasia 10.7
853 orofaciodigital syndrome i 10.7
854 muenke syndrome 10.7
855 osteonecrosis 10.7
856 anaplastic large cell lymphoma 10.7
857 vascular dementia 10.7
858 congenital hypothyroidism 10.7
859 hidradenitis suppurativa 10.7
860 mastitis 10.7
861 achalasia 10.7
862 amyotrophy, hereditary neuralgic 10.7
863 alopecia universalis congenita 10.7
864 ankyloblepharon-ectodermal defects-cleft lip/palate 10.7
865 birt-hogg-dube syndrome 10.7
866 ichthyosis hystrix, curth-macklin type 10.7
867 optic atrophy 3, autosomal dominant 10.7
868 megacystis-microcolon-intestinal hypoperistalsis syndrome 10.7
869 gonadal dysgenesis 10.7
870 neuroendocrine tumor 10.7
871 endosteal hyperostosis, autosomal dominant 10.7
872 cytomegalovirus infection 10.7
873 isolated growth hormone deficiency 10.7
874 pica disease 10.7
875 maturity-onset diabetes of the young 10.7
876 ovarian disease 10.7
877 mycosis fungoides 10.7
878 bone disease 10.7
879 febrile seizures 10.7
880 familial adenomatous polyposis 1 10.7
881 silver-russell syndrome 1 10.7
882 nijmegen breakage syndrome 10.7
883 conn's syndrome 10.7
884 allergic conjunctivitis 10.7
885 hyperparathyroidism 1 10.7
886 kniest dysplasia 10.7
887 cerebellar ataxia, mental retardation, and dysequilibrium syndrome 1 10.7
888 dihydrolipoamide dehydrogenase deficiency 10.7
889 brody myopathy 10.7
890 familial atrial fibrillation 10.7
891 dystonia 1, torsion, autosomal dominant 10.7
892 arachnoid cysts, intracranial 10.7
893 whiplash 10.7
894 joint laxity, short stature, and myopia 10.7
895 histoplasmosis 10.7
896 sick sinus syndrome 10.7
897 global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies 10.7
898 epidermolytic hyperkeratosis 10.7
899 pachyonychia congenita 3 10.7
900 oculodentodigital dysplasia 10.7
901 histidinemia 10.7
902 lama2-related muscular dystrophy 10.7
903 chromosome 20 trisomy 10.7
904 fuchs' endothelial dystrophy 10.7
905 vogt-koyanagi-harada disease 10.7
906 factor xiii deficiency 10.7
907 dystonia 12 10.7
908 hawkinsinuria 10.7
909 ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia 10.7
910 anemia, congenital dyserythropoietic, type ia 10.7
911 succinyl-coa:3-oxoacid-coa transferase deficiency 10.7
912 3-methylglutaconic aciduria, type i 10.7
913 opsismodysplasia 10.7
914 welander distal myopathy 10.7
915 anauxetic dysplasia 1 10.7
916 kabuki syndrome 1 10.7
917 costello syndrome 10.7
918 bernard-soulier syndrome 10.7
919 wolfram syndrome 10.7
920 hemolytic uremic syndrome, atypical 1 10.7
921 oral squamous cell carcinoma 10.7
922 odontoma 10.7
923 pancytopenia 10.7
924 hereditary leiomyomatosis and renal cell cancer 10.7
925 norrie disease 10.7
926 amnestic disorder 10.7
927 iga nephropathy 1 10.7
928 ocular albinism 10.7
929 navicular bone, accessory 10.7
930 jalili syndrome 10.7
931 dicarboxylic aminoaciduria 10.7
932 catel-manzke syndrome 10.7
933 perrault syndrome 10.7
934 optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy 10.7
935 inclusion body myositis 10.7
936 incontinentia pigmenti 10.7
937 arterial tortuosity syndrome 10.7
938 mayer-rokitansky-kuster-hauser syndrome 10.7
939 cholesterol embolism 10.7
940 periapical granuloma 10.7
941 sezary's disease 10.7
942 hypertriglyceridemia, familial 10.7
943 cerebellar ataxia, neuropathy, and vestibular areflexia syndrome 10.7
944 gastrointestinal stromal tumor 10.7
945 multiple epiphyseal dysplasia 10.7
946 acoustic neuroma 10.7
947 papillomatosis, confluent and reticulated 10.7
948 multiple system atrophy 1 10.7
949 adrenal adenoma 10.7
950 aortic valve insufficiency 10.7
951 spinocerebellar ataxia 7 10.7
952 schizencephaly 10.7
953 landau-kleffner syndrome 10.7
954 trigeminal neuralgia 10.7
955 porphyria cutanea tarda 10.7
956 adenoid cystic carcinoma 10.7
957 iga glomerulonephritis 10.7
958 ascaris lumbricoides infection 10.7
959 familial glucocorticoid deficiency 10.7
960 burkitt lymphoma 10.7
961 aromatase excess syndrome 10.7
962 metatropic dysplasia 10.7
963 albinism, oculocutaneous, type iii 10.7
964 kohlschutter-tonz syndrome 10.7
965 kaufman oculocerebrofacial syndrome 10.7
966 coenzyme q10 deficiency, primary, 1 10.7
967 majeed syndrome 10.7
968 tetralogy of fallot 10.7
969 cryptococcosis 10.7
970 albinism 10.7
971 hereditary angioedema 10.7
972 sickle cell anemia 10.7
973 coccidioidomycosis 10.7
974 ichthyosis, congenital, autosomal recessive 4b 10.7
975 shwachman-diamond syndrome 1 10.7
976 noonan syndrome with multiple lentigines 10.7
977 subacute thyroiditis 10.7
978 arthropathy 10.7
979 mucositis 10.7
980 ceroid lipofuscinosis, neuronal, 3 10.7
981 donohue syndrome 10.7
982 neuraminidase deficiency 10.7
983 multiple pterygium syndrome, escobar variant 10.7
984 pyruvate dehydrogenase e1-alpha deficiency 10.7
985 primary hyperparathyroidism 10.7
986 polymicrogyria 10.7
987 autoimmune hepatitis 10.7
988 dermatofibrosarcoma protuberans 10.7
989 anal fistula 10.7
990 bronchiolitis 10.7
991 factor v deficiency 10.7
992 coffin-lowry syndrome 10.7
993 diabetes mellitus, permanent neonatal 4 10.7
994 porencephaly 10.7
995 postural orthostatic tachycardia syndrome 10.7
996 oncocytoma 10.7
997 gallbladder cancer 10.7
998 kindler syndrome 10.7
999 megalocornea 10.7
1000 aural atresia, congenital 10.7
1001 2-hydroxyglutaric aciduria 10.7
1002 palindromic rheumatism 10.7
1003 myotonia congenita 10.7
1004 supravalvular aortic stenosis 10.7
1005 factor vii deficiency 10.7
1006 bartter disease 10.7
1007 chorea, childhood-onset, with psychomotor retardation 10.7
1008 mucormycosis 10.7
1009 spinal stenosis 10.7
1010 dysentery 10.7
1011 chiari malformation 10.7
1012 listeriosis 10.7
1013 jumping frenchmen of maine 10.7
1014 basal cell nevus syndrome 10.7
1015 werner syndrome 10.7
1016 lymphoplasmacytic lymphoma 10.7
1017 encephalopathy, progressive, early-onset, with episodic rhabdomyolysis 10.7
1018 dubin-johnson syndrome 10.7
1019 trimethylaminuria 10.7
1020 la crosse encephalitis 10.7
1021 rocky mountain spotted fever 10.7
1022 nemaline myopathy 10.7
1023 iridocyclitis 10.7
1024 alpha-thalassemia 10.7
1025 subvalvular aortic stenosis 10.7
1026 epiglottitis 10.7
1027 soft tissue sarcoma 10.7
1028 orthostatic intolerance 10.7
1029 subacute sclerosing panencephalitis 10.7
1030 churg-strauss syndrome 10.7
1031 mitochondrial dna depletion syndrome 4a 10.7
1032 jervell and lange-nielsen syndrome 1 10.7
1033 miller-dieker lissencephaly syndrome 10.7
1034 glycerol kinase deficiency 10.7
1035 glycine encephalopathy 10.7
1036 pontocerebellar hypoplasia 10.7
1037 multiple endocrine neoplasia, type iia 10.7
1038 tyrosinemia 10.7
1039 mixed connective tissue disease 10.7
1040 retinoschisis 1, x-linked, juvenile 10.7
1041 emery-dreifuss muscular dystrophy 10.7
1042 autosomal recessive congenital ichthyosis 10.7
1043 lactose intolerance 10.7
1044 testicular seminoma 10.7
1045 contractural arachnodactyly, congenital 10.7
1046 paramyotonia congenita of von eulenburg 10.7
1047 pelger-huet anomaly 10.7
1048 leukoencephalopathy, hereditary diffuse, with spheroids 10.7
1049 cholestasis, benign recurrent intrahepatic, 1 10.7
1050 glutathione synthetase deficiency 10.7
1051 glaucoma-related pigment dispersion syndrome 10.7
1052 myotonic dystrophy 2 10.7
1053 congenital chloride diarrhea 10.7
1054 anterior segment dysgenesis 10.7
1055 achondrogenesis 10.7
1056 salmonellosis 10.7
1057 lipoid congenital adrenal hyperplasia 10.7
1058 optic neuritis 10.7
1059 buruli ulcer 10.7
1060 adenosine deaminase deficiency 10.7
1061 pityriasis rosea 10.7
1062 impetigo 10.7
1063 cutaneous anthrax 10.7
1064 brooke-spiegler syndrome 10.7
1065 legius syndrome 10.7
1066 hypokalemia 10.7
1067 multiple endocrine neoplasia, type i 10.7
1068 t-cell lymphoma, subcutaneous panniculitis-like 10.7
1069 adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency 10.7
1070 osteoid osteoma 10.7
1071 inappropriate adh syndrome 10.7
1072 ceroid lipofuscinosis, neuronal, 2 10.7
1073 corneal dystrophy, gelatinous drop-like 10.7
1074 hypermethioninemia 10.7
1075 alpha thalassemia-x-linked intellectual disability syndrome 10.7
1076 gerstmann syndrome 10.7
1077 prothrombin-related thrombophilia 10.7
1078 developmental dysplasia of the hip 1 10.7
1079 holoprosencephaly 10.7
1080 osteochondritis dissecans 10.7
1081 congenital hepatic fibrosis 10.7
1082 hereditary hemorrhagic telangiectasia 10.7
1083 pituitary adenoma 10.7
1084 myoclonus 10.7
1085 pityriasis rubra pilaris 10.7
1086 premature ovarian failure 1 10.7
1087 kallmann syndrome 10.7
1088 turner syndrome 10.7
1089 rift valley fever 10.7
1090 hepatoblastoma 10.7
1091 cervical dystonia 10.7
1092 sialadenitis 10.7
1093 pseudomyxoma peritonei 10.7
1094 cutaneous t cell lymphoma 10.7
1095 seizures, benign familial neonatal, 1 10.7
1096 insulinoma 10.7
1097 hermansky-pudlak syndrome 10.7
1098 papillorenal syndrome 10.7
1099 corneal dystrophy, posterior polymorphous, 1 10.7
1100 craniofacial-deafness-hand syndrome 10.7
1101 arthropathy, progressive pseudorheumatoid, of childhood 10.7
1102 cranioectodermal dysplasia 1 10.7
1103 anemia, congenital dyserythropoietic, type ii 10.7
1104 fanconi-bickel syndrome 10.7
1105 mulibrey nanism 10.7
1106 chanarin-dorfman syndrome 10.7
1107 cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss 10.7
1108 au-kline syndrome 10.7
1109 tetrahydrobiopterin deficiency 10.7
1110 fibular hemimelia 10.7
1111 arteriosclerosis 10.7
1112 gaucher's disease 10.7
1113 bronchiectasis 10.7
1114 cone-rod dystrophy 2 10.7
1115 familial hypocalciuric hypercalcemia 10.7
1116 episodic ataxia 10.7
1117 porphyria, acute intermittent 10.7
1118 hyperostosis 10.7
1119 filariasis 10.7
1120 patau syndrome 10.7
1121 carnitine deficiency, systemic primary 10.7
1122 cystathioninuria 10.7
1123 langer mesomelic dysplasia 10.7
1124 gm2-gangliosidosis, ab variant 10.7
1125 epileptic encephalopathy, early infantile, 2 10.7
1126 46,xx sex reversal 1 10.7
1127 mitochondrial trifunctional protein deficiency 10.7
1128 corticosterone methyloxidase type ii deficiency 10.7
1129 bestrophinopathy, autosomal recessive 10.7
1130 hyperprolinemia 10.7
1131 absence of septum pellucidum 10.7
1132 alopecia areata 10.7
1133 early infantile epileptic encephalopathy 10.7
1134 factor x deficiency 10.7
1135 pyoderma gangrenosum 10.7
1136 lactic acidosis 10.7
1137 dermatitis herpetiformis 10.7
1138 postherpetic neuralgia 10.7
1139 autoimmune polyendocrine syndrome, type i, with or without reversible metaphyseal dysplasia 10.7
1140 isolated growth hormone deficiency, type ia 10.7
1141 umbilical hernia 10.7
1142 microscopic polyangiitis 10.7
1143 dystonia, dopa-responsive 10.7
1144 trichodentoosseous syndrome 10.7
1145 bietti crystalline corneoretinal dystrophy 10.7
1146 n-acetylglutamate synthase deficiency 10.7
1147 pyropoikilocytosis, hereditary 10.7
1148 sea-blue histiocyte disease 10.7
1149 tyrosinemia, type ii 10.7
1150 partington x-linked mental retardation syndrome 10.7
1151 genitopatellar syndrome 10.7
1152 anterior segment dysgenesis 2 10.7
1153 geleophysic dysplasia 10.7
1154 sporadic hemiplegic migraine 10.7
1155 dermatomyositis 10.7
1156 cystic lymphangioma 10.7
1157 legg-calve-perthes disease 10.7
1158 chorioamnionitis 10.7
1159 mastoiditis 10.7
1160 monoclonal gammopathy of uncertain significance 10.7
1161 cleft lip/palate 10.7
1162 variegate porphyria 10.7
1163 achromatopsia 10.7
1164 orofaciodigital syndrome 10.7
1165 trichotillomania 10.7
1166 tracheoesophageal fistula with or without esophageal atresia 10.7
1167 carbonic anhydrase va deficiency, hyperammonemia due to 10.7
1168 broken heart syndrome 10.7
1169 alopecia, androgenetic, 1 10.7
1170 ichthyosis, x-linked 10.7
1171 myeloid sarcoma 10.7
1172 glucose intolerance 10.7
1173 decubitus ulcer 10.7
1174 corticobasal degeneration 10.7
1175 chordoma 10.7
1176 frontotemporal dementia and/or amyotrophic lateral sclerosis 1 10.7
1177 corneal dystrophy, lattice type i 10.7
1178 beare-stevenson cutis gyrata syndrome 10.7
1179 spinocerebellar ataxia 34 10.7
1180 lacrimoauriculodentodigital syndrome 10.7
1181 vasculopathy, retinal, with cerebral leukodystrophy 10.7
1182 glucocorticoid deficiency 1 10.7
1183 hyperornithinemia-hyperammonemia-homocitrullinuria syndrome 10.7
1184 mucopolysaccharidosis, type iiic 10.7
1185 cerebral creatine deficiency syndrome 1 10.7
1186 exudative vitreoretinopathy 2, x-linked 10.7
1187 renpenning syndrome 1 10.7
1188 d-2-hydroxyglutaric aciduria 1 10.7
1189 czech dysplasia 10.7
1190 isobutyryl-coa dehydrogenase deficiency 10.7
1191 dystonia 16 10.7
1192 cerebroretinal microangiopathy with calcifications and cysts 1 10.7
1193 autoinflammation, panniculitis, and dermatosis syndrome 10.7
1194 3mc syndrome 10.7
1195 marie unna congenital hypotrichosis 10.7
1196 crigler-najjar syndrome, type i 10.7
1197 zellweger syndrome 10.7
1198 lymphangioma 10.7
1199 aortic aneurysm, familial thoracic 1 10.7
1200 lemierre's syndrome 10.7
1201 hypersplenism 10.7
1202 polydactyly 10.7
1203 thanatophoric dysplasia, type i 10.7
1204 retinitis pigmentosa 10.7
1205 limb ischemia 10.7
1206 meniere disease 10.7
1207 muscular dystrophy, becker type 10.7
1208 diverticulitis 10.7
1209 goodpasture syndrome 10.7
1210 citrullinemia, type ii, adult-onset 10.7
1211 opsoclonus-myoclonus syndrome 10.7
1212 intestinal disease 10.7
1213 progressive multifocal leukoencephalopathy 10.7
1214 keratoconus 10.7
1215 tularemia 10.7
1216 angioedema 10.7
1217 niemann-pick disease, type c2 10.7
1218 hereditary sensory neuropathy 10.7
1219 radioulnar synostosis 10.7
1220 familial colorectal cancer 10.7
1221 mccune-albright syndrome 10.7
1222 adjustment disorder 10.7
1223 schnyder corneal dystrophy 10.7
1224 corneal dystrophy, meesmann, 1 10.7
1225 anterior segment dysgenesis 4 10.7
1226 osteoglophonic dysplasia 10.7
1227 medullary cystic kidney disease 1 10.7
1228 adrenal hyperplasia, congenital, due to 17-alpha-hydroxylase deficiency 10.7
1229 ehlers-danlos syndrome, dermatosparaxis type 10.7
1230 keutel syndrome 10.7
1231 mannosidosis, beta a, lysosomal 10.7
1232 carnitine palmitoyltransferase i deficiency 10.7
1233 atelosteogenesis, type ii 10.7
1234 phosphoglycerate kinase 1 deficiency 10.7
1235 achondrogenesis, type ib 10.7
1236 phosphoglycerate dehydrogenase deficiency 10.7
1237 ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy 10.7
1238 rippling muscle disease 2 10.7
1239 schindler disease, type i 10.7
1240 obesity, early-onset, with adrenal insufficiency and red hair 10.7
1241 bleeding disorder, platelet-type, 11 10.7
1242 combined malonic and methylmalonic aciduria 10.7
1243 3-methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome 10.7
1244 asparagine synthetase deficiency 10.7
1245 dopamine beta-hydroxylase deficiency 10.7
1246 familial thoracic aortic aneurysm and aortic dissection 10.7
1247 recurrent hydatidiform mole 10.7
1248 glucose phosphate isomerase deficiency 10.7
1249 thyroid cancer, nonmedullary, 1 10.7
1250 iron deficiency anemia 10.7
1251 poems syndrome 10.7
1252 van der woude syndrome 1 10.7
1253 nail-patella syndrome 10.7
1254 hyperlipoproteinemia, type i 10.7
1255 hemoglobin h disease 10.7
1256 hyperacusis 10.7
1257 anoxia 10.7
1258 inflammatory breast carcinoma 10.7
1259 pulmonary sequestration 10.7
1260 thoracic outlet syndrome 10.7
1261 pneumoconiosis 10.7
1262 usher syndrome, type i 10.7
1263 sacral defect with anterior meningocele 10.7
1264 alternating hemiplegia of childhood 10.7
1265 acute flaccid myelitis 10.7
1266 cervix uteri carcinoma in situ 10.7
1267 isolated pierre robin sequence 10.7
1268 hepatitis e 10.7
1269 smallpox 10.7
1270 arteriovenous malformations of the brain 10.7
1271 brachial plexus lesion 10.7
1272 pachyonychia congenita 1 10.7
1273 mucolipidosis ii alpha/beta 10.7
1274 lissencephaly 1 10.7
1275 stickler syndrome 10.7
1276 geographic tongue 10.7
1277 hemimegalencephaly 10.7
1278 ohtahara syndrome 10.7
1279 bursitis 10.7
1280 paraganglioma 10.7
1281 epidermoid cysts 10.7
1282 hepatic encephalopathy 10.7
1283 mastocytosis, cutaneous 10.7
1284 parathyroid carcinoma 10.7
1285 peripartum cardiomyopathy 10.7
1286 adrenal carcinoma 10.7
1287 long qt syndrome 1 10.7
1288 mitochondrial complex iv deficiency 10.7
1289 mannosidosis, alpha b, lysosomal 10.7
1290 cinca syndrome 10.7
1291 pick disease of brain 10.7
1292 bilirubin metabolic disorder 10.7
1293 thrombophilia due to activated protein c resistance 10.7
1294 retrograde amnesia 10.7
1295 metaphyseal chondrodysplasia, schmid type 10.7
1296 moebius syndrome 10.7
1297 apparent mineralocorticoid excess 10.7
1298 meckel syndrome, type 1 10.7
1299 ovarian small cell carcinoma 10.7
1300 neurofibroma 10.7
1301 cerebellar hypoplasia 10.7
1302 protein c deficiency 10.7
1303 epidermolysis bullosa dystrophica 10.7
1304 fryns syndrome 10.7
1305 rothmund-thomson syndrome, type 1 10.7
1306 hhv-6 encephalitis 10.7
1307 vitiligo-associated multiple autoimmune disease susceptibility 6 10.7
1308 hypoplastic left heart syndrome 10.7
1309 diabetes mellitus, type i 10.7
1310 cor triatriatum 10.7
1311 acrodermatitis enteropathica, zinc-deficiency type 10.7
1312 pustular psoriasis 10.7
1313 hypoascorbemia 10.7
1314 physical disorder 10.7
1315 lysosomal storage disease 10.7
1316 graves disease 1 10.7
1317 coffin-siris syndrome 1 10.7
1318 fundus albipunctatus 10.7
1319 hypochondroplasia 10.7
1320 laryngeal cleft 10.7
1321 alport syndrome 10.7
1322 newcastle disease 10.7
1323 muscular dystrophy, congenital, lmna-related 10.7
1324 oculocutaneous albinism 10.7
1325 invasive aspergillosis 10.7
1326 small cell carcinoma 10.7
1327 achalasia-addisonianism-alacrima syndrome 10.7
1328 pseudopseudohypoparathyroidism 10.7
1329 congenital fiber-type disproportion 10.7
1330 giant axonal neuropathy 10.7
1331 tendinitis 10.7
1332 actinomycosis 10.7
1333 diabetes insipidus, nephrogenic, autosomal 10.7
1334 polycythemia 10.7
1335 postpartum depression 10.7
1336 variola major 10.7
1337 hyperphosphatemia 10.7
1338 q fever 10.7
1339 pharyngitis 10.7
1340 buschke-ollendorff syndrome 10.7
1341 fucosidosis 10.7
1342 l-2-hydroxyglutaric aciduria 10.7
1343 niemann-pick disease, type b 10.7
1344 spermatogenic failure 9 10.7
1345 adams-oliver syndrome 10.7
1346 essential tremor 10.7
1347 mammary paget's disease 10.7
1348 pulmonary fibrosis, idiopathic 10.7
1349 miyoshi muscular dystrophy 1 10.7
1350 pityriasis lichenoides et varioliformis acuta 10.7
1351 epilepsy, myoclonic juvenile 10.7
1352 childhood acute lymphocytic leukemia 10.7
1353 hemorrhoid 10.7
1354 henoch-schoenlein purpura 10.7
1355 cockayne syndrome 10.7
1356 pulmonary arteriovenous malformation 10.7
1357 yellow fever 10.7
1358 anogenital venereal wart 10.7
1359 trichorhinophalangeal syndrome, type ii 10.7
1360 multiple sulfatase deficiency 10.7
1361 spondyloepiphyseal dysplasia tarda, x-linked 10.7
1362 psychogenic movement 10.7
1363 endocardial fibroelastosis 10.7
1364 uremia 10.7
1365 renal tubular acidosis 10.7
1366 frontotemporal lobar degeneration with tdp43 inclusions, grn-related 10.7
1367 blastomycosis 10.7
1368 normal pressure hydrocephalus 10.7
1369 choriocarcinoma 10.7
1370 pyogenic granuloma 10.7
1371 cardiofaciocutaneous syndrome 1 10.7
1372 craniometaphyseal dysplasia, autosomal dominant 10.7
1373 spastic ataxia, charlevoix-saguenay type 10.7
1374 muscular dystrophy-dystroglycanopathy , type c, 5 10.7
1375 pitt-hopkins syndrome 10.7
1376 cerebral cavernous malformation, familial 10.7
1377 neonatal adrenoleukodystrophy 10.7
1378 warty dyskeratoma 10.7
1379 otosclerosis 10.7
1380 epileptic encephalopathy, early infantile, 6 10.7
1381 keratomalacia 10.7
1382 nephrocalcinosis 10.7
1383 dyslexia 10.7
1384 swine influenza 10.7
1385 polyhydramnios 10.7
1386 chediak-higashi syndrome 10.7
1387 spastic paraplegia, intellectual disability, nystagmus, and obesity 10.7
1388 pallister-hall syndrome 10.7
1389 precocious puberty, male-limited 10.7
1390 whim syndrome 10.7
1391 gaucher disease, type ii 10.7
1392 diarrhea 2, with microvillus atrophy 10.7
1393 mucopolysaccharidosis, type iiia 10.7
1394 enhanced s-cone syndrome 10.7
1395 melnick-needles syndrome 10.7
1396 spinocerebellar ataxia 8 10.7
1397 primary pigmented nodular adrenocortical disease 10.7
1398 egg allergy 10.7
1399 auditory neuropathy spectrum disorder 10.7
1400 binswanger's disease 10.7
1401 pediatric acute-onset neuropsychiatric syndrome 10.7
1402 polycystic kidney disease 4 with or without polycystic liver disease 10.6
1403 hypophosphatemic rickets, x-linked recessive 10.6
1404 infantile myofibromatosis 10.6
1405 cornelia de lange syndrome 10.6
1406 waardenburg's syndrome 10.6
1407 neuroleptic malignant syndrome 10.6
1408 retinal degeneration 10.6
1409 hemolytic-uremic syndrome 10.6
1410 oropharynx cancer 10.6
1411 substance dependence 10.6
1412 hyperaldosteronism, familial, type i 10.6
1413 branchiooculofacial syndrome 10.6
1414 craniosynostosis 1 10.6
1415 schimmelpenning-feuerstein-mims syndrome 10.6
1416 osteogenesis imperfecta, type iv 10.6
1417 carpenter syndrome 1 10.6
1418 hypouricemia, renal, 1 10.6
1419 roberts syndrome 10.6
1420 histiocytosis-lymphadenopathy plus syndrome 10.6
1421 glucose/galactose malabsorption 10.6
1422 griscelli syndrome, type 2 10.6
1423 acrocapitofemoral dysplasia 10.6
1424 frontometaphyseal dysplasia 10.6
1425 dysplastic nevus syndrome 10.6
1426 adult polyglucosan body disease 10.6
1427 glucose transporter type 1 deficiency syndrome 10.6
1428 adenosarcoma of the uterus 10.6
1429 staphylococcal toxic shock syndrome 10.6
1430 alkuraya-kucinskas syndrome 10.6
1431 apert syndrome 10.6
1432 lesch-nyhan syndrome 10.6
1433 adenomyosis 10.6
1434 necrotizing fasciitis 10.6
1435 pituitary tumors 10.6
1436 dementia, lewy body 10.6
1437 immunodysregulation, polyendocrinopathy, and enteropathy, x-linked 10.6
1438 esophageal candidiasis 10.6
1439 corneal dystrophy, epithelial basement membrane 10.6
1440 renal cysts and diabetes syndrome 10.6
1441 acyl-coa dehydrogenase, short-chain, deficiency of 10.6
1442 meier-gorlin syndrome 1 10.6
1443 ehlers-danlos syndrome, kyphoscoliotic type, 1 10.6
1444 galactosemia iii 10.6
1445 vas deferens, congenital bilateral aplasia of 10.6
1446 weaver syndrome 10.6
1447 osteopathia striata with cranial sclerosis 10.6
1448 anemia, sideroblastic, and spinocerebellar ataxia 10.6
1449 immunodeficiency with hyper-igm, type 1 10.6
1450 hypogonadotropic hypogonadism 1 with or without anosmia 10.6
1451 cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 10.6
1452 segawa syndrome, autosomal recessive 10.6
1453 parkinsonism-dystonia, infantile, 1 10.6
1454 thrombocytopenia 5 10.6
1455 rahman syndrome 10.6
1456 primary hypomagnesemia 10.6
1457 prothrombin deficiency 10.6
1458 otopalatodigital syndrome, type i 10.6
1459 pleuropulmonary blastoma 10.6
1460 intrahepatic cholestasis of pregnancy 10.6
1461 empty sella syndrome 10.6
1462 megacolon 10.6
1463 fascioliasis 10.6
1464 schopf-schulz-passarge syndrome 10.6
1465 dyskeratosis congenita 10.6
1466 anaplastic ependymoma 10.6
1467 epidemic typhus 10.6
1468 oculopharyngeal muscular dystrophy 10.6
1469 impulse control disorder 10.6
1470 malignant teratoma 10.6
1471 erythromelalgia 10.6
1472 ameloblastoma 10.6
1473 coloboma of macula 10.6
1474 alzheimer disease 2 10.6
1475 brachydactyly, type e1 10.6
1476 myopathy, distal, 1 10.6
1477 dyggve-melchior-clausen disease 10.6
1478 gapo syndrome 10.6
1479 carbamoyl phosphate synthetase i deficiency, hyperammonemia due to 10.6
1480 muscular dystrophy, limb-girdle, autosomal recessive 2 10.6
1481 nuchal bleb, familial 10.6
1482 postaxial acrofacial dysostosis 10.6
1483 chromosome xq26.3 duplication syndrome 10.6
1484 wiedemann-steiner syndrome 10.6
1485 spinocerebellar ataxia 15 10.6
1486 hypotrichosis-lymphedema-telangiectasia syndrome 10.6
1487 cholesterol ester storage disease 10.6
1488 oguchi disease 10.6
1489 panbronchiolitis, diffuse 10.6
1490 scheie syndrome 10.6
1491 klippel-feil syndrome 10.6
1492 tetraploidy 10.6
1493 autoimmune pancreatitis 10.6
1494 adult t-cell leukemia 10.6
1495 leiomyoma, uterine 10.6
1496 zollinger-ellison syndrome 10.6
1497 severe congenital neutropenia 10.6
1498 aspiration pneumonia 10.6
1499 cystadenoma 10.6
1500 fibromuscular dysplasia 10.6
1501 adrenomyeloneuropathy 10.6
1502 spondyloepiphyseal dysplasia with congenital joint dislocations 10.6
1503 afibrinogenemia, congenital 10.6
1504 hydranencephaly 10.6
1505 hereditary amyloidosis 10.6
1506 hydrops fetalis, nonimmune 10.6
1507 tylosis with esophageal cancer 10.6
1508 microcephaly with or without chorioretinopathy, lymphedema, or mental retardation 10.6
1509 feingold syndrome 1 10.6
1510 watson syndrome 10.6
1511 achondrogenesis, type ii 10.6
1512 coach syndrome 10.6
1513 d-glyceric aciduria 10.6
1514 hyaline fibromatosis syndrome 10.6
1515 3-hydroxyacyl-coa dehydrogenase deficiency 10.6
1516 hydroxyprolinemia 10.6
1517 restrictive dermopathy, lethal 10.6
1518 blue cone monochromacy 10.6
1519 stuve-wiedemann syndrome 10.6
1520 acromesomelic dysplasia, maroteaux type 10.6
1521 kufor-rakeb syndrome 10.6
1522 polymicrogyria, bilateral frontoparietal 10.6
1523 chromosome 22q11.2 duplication syndrome 10.6
1524 mandibulofacial dysostosis, guion-almeida type 10.6
1525 intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies 10.6
1526 triosephosphate isomerase deficiency 10.6
1527 thrombocytopenia 6 10.6
1528 hypoalphalipoproteinemia, primary, 2 10.6
1529 adenoiditis 10.6
1530 astereognosia 10.6
1531 atypical werner syndrome 10.6
1532 hemoglobin zurich 10.6
1533 punctate inner choroidopathy 10.6
1534 leber optic atrophy 10.6
1535 separation anxiety disorder 10.6
1536 craniofacial microsomia 10.6
1537 spasmodic dysphonia 10.6
1538 glaucoma, primary open angle 10.6
1539 hypoparathyroidism 10.6
1540 exostosis 10.6
1541 exostoses, multiple, type i 10.6
1542 persistent mullerian duct syndrome 10.6
1543 agraphia 10.6
1544 hydatidiform mole, recurrent, 1 10.6
1545 gastroparesis 10.6
1546 alveolar echinococcosis 10.6
1547 ossifying fibroma 10.6
1548 pycnodysostosis 10.6
1549 neuronal ceroid-lipofuscinoses 10.6
1550 polycystic liver disease 10.6
1551 grade iii astrocytoma 10.6
1552 oral submucous fibrosis 10.6
1553 eosinophilic pneumonia 10.6
1554 scarlet fever 10.6
1555 anus, imperforate 10.6
1556 optic nerve hypoplasia, bilateral 10.6
1557 spinocerebellar ataxia 2 10.6
1558 chronic active epstein-barr virus infection 10.6
1559 paraneoplastic pemphigus 10.6
1560 drug allergy 10.6
1561 castleman disease 10.6
1562 brachydactyly, type a1 10.6
1563 brachydactyly, type c 10.6
1564 spinocerebellar ataxia 29 10.6
1565 ichthyosis bullosa of siemens 10.6
1566 macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss 10.6
1567 char syndrome 10.6
1568 folate malabsorption, hereditary 10.6
1569 geleophysic dysplasia 1 10.6
1570 hartnup disorder 10.6
1571 woodhouse-sakati syndrome 10.6
1572 malonyl-coa decarboxylase deficiency 10.6
1573 bartsocas-papas syndrome 10.6
1574 ogden syndrome 10.6
1575 masa syndrome 10.6
1576 amegakaryocytic thrombocytopenia, congenital 10.6
1577 hyperinsulinemic hypoglycemia, familial, 6 10.6
1578 paraganglioma and gastric stromal sarcoma 10.6
1579 immunodeficiency, common variable, 1 10.6
1580 posterior column ataxia with retinitis pigmentosa 10.6
1581 fontaine progeroid syndrome 10.6
1582 microcephaly-capillary malformation syndrome 10.6
1583 hypomyelination with brainstem and spinal cord involvement and leg spasticity 10.6
1584 mitochondrial dna depletion syndrome 13 10.6
1585 myopathy due to myoadenylate deaminase deficiency 10.6
1586 autoimmune lymphoproliferative syndrome, type iii 10.6
1587 sideroblastic anemia with b-cell immunodeficiency, periodic fevers, and developmental delay 10.6
1588 brachyolmia 10.6
1589 tactile agnosia 10.6
1590 uv-sensitive syndrome 10.6
1591 christianson syndrome 10.6
1592 large congenital melanocytic nevus 10.6
1593 cerebro-oculo-facio-skeletal syndrome 10.6
1594 kyphoscoliotic ehlers-danlos syndrome 10.6
1595 benign ependymoma 10.6
1596 hearing loss, noise-induced 10.6
1597 currarino syndrome 10.6
1598 autoimmune lymphoproliferative syndrome, type v 10.6
1599 ileitis 10.6
1600 raynaud disease 10.6
1601 hyperoxaluria, primary, type i 10.6
1602 t-cell large granular lymphocyte leukemia 10.6
1603 cone dystrophy 10.6
1604 anovulation 10.6
1605 erythrokeratoderma ''en cocardes'' 10.6
1606 hypopituitarism 10.6
1607 polymyositis 10.6
1608 reye syndrome 10.6
1609 cherubism 10.6
1610 multiple endocrine neoplasia, type iib 10.6
1611 hemihyperplasia, isolated 10.6
1612 jejunal atresia 10.6
1613 acanthoma 10.6
1614 carotid artery disease 10.6
1615 epicondylitis 10.6
1616 neuronal ceroid lipofuscinosis 10.6
1617 mucopolysaccharidosis iii 10.6
1618 chronic mucocutaneous candidiasis 10.6
1619 bap1 tumor predisposition syndrome 10.6
1620 megalencephaly 10.6
1621 choreatic disease 10.6
1622 testicular cancer 10.6
1623 phaeohyphomycosis 10.6
1624 brachydactyly, type a2 10.6
1625 jackson-weiss syndrome 10.6
1626 dystonia 4, torsion, autosomal dominant 10.6
1627 transient bullous dermolysis of the newborn 10.6
1628 macular dystrophy, vitelliform, 2 10.6
1629 marshall syndrome 10.6
1630 arthrogryposis, distal, type 7 10.6
1631 cutis laxa, autosomal recessive, type iia 10.6
1632 focal facial dermal dysplasia 3, setleis type 10.6
1633 peho syndrome 10.6
1634 craniofrontonasal syndrome 10.6
1635 orofacial cleft 11 10.6
1636 seizures, benign familial infantile, 1 10.6
1637 spinocerebellar ataxia 11 10.6
1638 transaldolase deficiency 10.6
1639 osteopetrosis, autosomal dominant 1 10.6
1640 irak4 deficiency 10.6
1641 pontocerebellar hypoplasia, type 3 10.6
1642 pyruvate dehydrogenase phosphatase deficiency 10.6
1643 leukodystrophy, hypomyelinating, 2 10.6
1644 cataract 21, multiple types 10.6
1645 thiopurines, poor metabolism of, 1 10.6
1646 salih myopathy 10.6
1647 glycogen storage disease xii 10.6
1648 riddle syndrome 10.6
1649 coenzyme q10 deficiency, primary, 4 10.6
1650 kahrizi syndrome 10.6
1651 leukoencephalopathy, cystic, without megalencephaly 10.6
1652 chromosome 17q12 duplication syndrome 10.6
1653 osteogenesis imperfecta, type xiii 10.6
1654 combined oxidative phosphorylation deficiency 12 10.6
1655 exudative vitreoretinopathy 6 10.6
1656 spastic paraplegia and psychomotor retardation with or without seizures 10.6
1657 cerebral creatine deficiency syndrome 10.6
1658 baraitser-winter syndrome 10.6
1659 46,xx sex reversal 10.6
1660 horizontal gaze palsy with progressive scoliosis 10.6
1661 pdgfrb-associated chronic eosinophilic leukemia 10.6
1662 tetra-amelia syndrome 10.6
1663 myoclonic encephalopathy of infants 10.6
1664 esophageal varix 10.6
1665 orbital cellulitis 10.6
1666 hypercalcemia, infantile, 1 10.6
1667 severe combined immunodeficiency, x-linked 10.6
1668 skin tag 10.6
1669 multiple endocrine neoplasia 10.6
1670 neurotic disorder 10.6
1671 chronic inflammatory demyelinating polyradiculoneuropathy 10.6
1672 insensitivity to pain, congenital, with anhidrosis 10.6
1673 scleredema adultorum 10.6
1674 eagle syndrome 10.6
1675 embryonal carcinoma 10.6
1676 osteochondroma 10.6
1677 ankyloglossia with or without tooth anomalies 10.6
1678 trichorhinophalangeal syndrome, type i 10.6
1679 psoriasis 14, pustular 10.6
1680 endometriosis of ovary 10.6
1681 pityriasis lichenoides 10.6
1682 congenital toxoplasmosis 10.6
1683 arachnoiditis 10.6
1684 cyclic neutropenia 10.6
1685 muckle-wells syndrome 10.6
1686 hemoglobin e disease 10.6
1687 heart valve disease 10.6
1688 immunoglobulin alpha deficiency 10.6
1689 leech infestation 10.6
1690 dysphasia, familial developmental 10.6
1691 malignant peripheral nerve sheath tumor 10.6
1692 mycobacterium fortuitum 10.6
1693 crohn's colitis 10.6
1694 poland syndrome 10.6
1695 corpus callosum, agenesis of 10.6
1696 crest syndrome 10.6
1697 metaphyseal dysplasia 10.6
1698 osteopoikilosis 10.6
1699 pseudoangiomatous stromal hyperplasia 10.6
1700 malakoplakia 10.6
1701 adult-onset still's disease 10.6
1702 lowe oculocerebrorenal syndrome 10.6
1703 kleptomania 10.6
1704 neurilemmomatosis 10.6
1705 luteoma 10.6
1706 retinal disease 10.6
1707 gallbladder disease 10.6
1708 pulmonary alveolar proteinosis 10.6
1709 corneal ulcer 10.6
1710 pancreas, annular 10.6
1711 chronic myelomonocytic leukemia 10.6
1712 meningococcal infection 10.6
1713 hyper-igd syndrome 10.6
1714 convulsions, familial infantile, with paroxysmal choreoathetosis 10.6
1715 delayed sleep phase disorder 10.6
1716 hirschsprung disease 1 10.6
1717 myelopathy, htlv-1-associated 10.6
1718 tropical spastic paraparesis 10.6
1719 short bowel syndrome 10.6
1720 cholesteatoma of middle ear 10.6
1721 ocular hypertension 10.6
1722 atrioventricular septal defect 10.6
1723 epidural abscess 10.6
1724 precocious puberty 10.6
1725 osteogenesis imperfecta, type ii 10.6
1726 dent disease 1 10.6
1727 alpha-thalassemia/mental retardation syndrome, x-linked 10.6
1728 hypophosphatemic rickets, x-linked dominant 10.6
1729 chops syndrome 10.6
1730 aniseikonia 10.6
1731 exudative vitreoretinopathy 10.6
1732 osteomalacia 10.6
1733 bile duct cancer 10.6
1734 collagen disease 10.6
1735 erythroleukemia, familial 10.6
1736 thrombotic thrombocytopenic purpura 10.6
1737 hemangioendothelioma 10.6
1738 reflex sympathetic dystrophy 10.6
1739 relapsing polychondritis 10.6
1740 pseudohypoparathyroidism, type ia 10.6
1741 thyroid crisis 10.6
1742 trisomy 22 10.6
1743 anaplastic oligoastrocytoma 10.6
1744 virus-associated trichodysplasia spinulosa 10.6
1745 carcinosarcoma 10.6
1746 dentinogenesis imperfecta type 2 10.6
1747 rheumatic heart disease 10.6
1748 leukoplakia 10.6
1749 hyperparathyroidism 2 with jaw tumors 10.6
1750 aromatase deficiency 10.6
1751 acute posterior multifocal placoid pigment epitheliopathy 10.6
1752 epidermoid brain cyst 10.6
1753 hemophilic arthropathy 10.6
1754 iritis 10.6
1755 salpingitis 10.6
1756 limbic encephalitis 10.6
1757 mantle cell lymphoma 10.6
1758 hydrocele 10.6
1759 fournier gangrene 10.6
1760 lennox-gastaut syndrome 10.6
1761 osteogenesis imperfecta, type i 10.6
1762 spinocerebellar ataxia 6 10.6
1763 polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1 10.6
1764 lipoid proteinosis of urbach and wiethe 10.6
1765 primary autosomal recessive microcephaly 10.6
1766 splenic disease 10.6
1767 autoimmune inner ear disease 10.6
1768 autosomal dominant cerebellar ataxia 10.6
1769 pseudohermaphroditism 10.6
1770 chronic thromboembolic pulmonary hypertension 10.6
1771 amyloidosis aa 10.6
1772 diabetes insipidus, neurohypophyseal 10.6
1773 ehlers-danlos syndrome, vascular type 10.6
1774 gerstmann-straussler disease 10.6
1775 palmoplantar keratoderma, epidermolytic 10.6
1776 prolidase deficiency 10.6
1777 choreoacanthocytosis 10.6
1778 dysfibrinogenemia, congenital 10.6
1779 membranous nephropathy 10.6
1780 stuttering 10.6
1781 adrenal cortical adenocarcinoma 10.6
1782 intestinal pseudo-obstruction 10.6
1783 retinal ischemia 10.6
1784 posterior uveitis 10.6
1785 primary angle-closure glaucoma 10.6
1786 atypical teratoid rhabdoid tumor 10.6
1787 tooth agenesis 10.6
1788 vater/vacterl association 10.6
1789 denys-drash syndrome 10.6
1790 walker-warburg syndrome 10.6
1791 autosomal recessive pyridoxine-refractory sideroblastic anemia 2 10.6
1792 superior semicircular canal dehiscence 10.6
1793 cakut 10.6
1794 sitosterolemia 10.6
1795 campylobacteriosis 10.6
1796 adult respiratory distress syndrome 10.6
1797 late-onset retinal degeneration 10.6
1798 renal osteodystrophy 10.6
1799 cowpox 10.6
1800 enchondroma 10.6
1801 ocular toxoplasmosis 10.6
1802 paraneoplastic syndromes 10.6
1803 brain cancer 10.6
1804 vesicoureteral reflux 1 10.6
1805 dirofilariasis 10.6
1806 status asthmaticus 10.6
1807 hajdu-cheney syndrome 10.6
1808 frasier syndrome 10.6
1809 bethlem myopathy 1 10.6
1810 enchondromatosis, multiple, ollier type 10.6
1811 isolated growth hormone deficiency, type ii 10.6
1812 succinic semialdehyde dehydrogenase deficiency 10.6
1813 cardiomyopathy, infantile histiocytoid 10.6
1814 juvenile absence epilepsy 10.6
1815 robinow syndrome 10.6
1816 parietal foramina 10.6
1817 mutyh polyposis 10.6
1818 diphallia 10.6
1819 fryns microphthalmia syndrome 10.6
1820 fusariosis 10.6
1821 complete androgen insensitivity syndrome 10.6
1822 retinal dystrophy, iris coloboma, and comedogenic acne syndrome 10.6
1823 chromosome 5q deletion syndrome 10.6
1824 vertical talus, congenital 10.6
1825 muscular dystrophy, limb-girdle, autosomal recessive 1 10.6
1826 mcleod syndrome 10.6
1827 glaucoma, normal tension 10.6
1828 crigler-najjar syndrome, type ii 10.6
1829 spinocerebellar ataxia 17 10.6
1830 hereditary mixed polyposis syndrome 10.6
1831 attenuated familial adenomatous polyposis 10.6
1832 hyperprolactinemia 10.6
1833 pulmonary arteriovenous fistulas 10.6
1834 epilepsy, idiopathic generalized 10.6
1835 generalized epilepsy with febrile seizures plus 10.6
1836 lymphangitis 10.6
1837 silicosis 10.6
1838 dacryocystitis 10.6
1839 myelomeningocele 10.6
1840 malignant hyperthermia 10.6
1841 polyploidy 10.6
1842 coronary artery dissection, spontaneous 10.6
1843 acrofacial dysostosis 1, nager type 10.6
1844 spinal muscular atrophy, type iii 10.6
1845 chondrodysplasia punctata 2, x-linked dominant 10.6
1846 desmosterolosis 10.6
1847 citrullinemia, type ii, neonatal-onset 10.6
1848 prothrombin deficiency, congenital 10.6
1849 butyrylcholinesterase deficiency 10.6
1850 asphyxiating thoracic dystrophy 10.6
1851 synpolydactyly 10.6
1852 acromesomelic dysplasia 10.6
1853 kleefstra syndrome 10.6
1854 46,xy sex reversal 10.6
1855 choline deficiency disease 10.6
1856 49, xxxxy syndrome 10.6
1857 nephrolithiasis, calcium oxalate 10.6
1858 mammographic density 10.6
1859 microsporidiosis 10.6
1860 aneurysmal bone cysts 10.6
1861 hypophosphatemia 10.6
1862 dumping syndrome 10.6
1863 thrombotic microangiopathy 10.6
1864 lissencephaly 10.6
1865 left ventricular noncompaction 10.6
1866 kernicterus 10.6
1867 genital herpes 10.6
1868 osseous heteroplasia, progressive 10.6
1869 emery-dreifuss muscular dystrophy 2, autosomal dominant 10.6
1870 stormorken syndrome 10.6
1871 acth-independent macronodular adrenal hyperplasia 10.6
1872 muscular dystrophy-dystroglycanopathy , type a, 4 10.6
1873 ceroid lipofuscinosis, neuronal, 1 10.6
1874 occipital horn syndrome 10.6
1875 dystonia 3, torsion, x-linked 10.6
1876 spinocerebellar ataxia 10 10.6
1877 leukoencephalopathy with vanishing white matter 10.6
1878 coenzyme q10 deficiency disease 10.6
1879 corpus luteum cyst 10.6
1880 diabetes mellitus, 6q24-related transient neonatal 10.6
1881 peanut allergy 10.6
1882 thyroid carcinoma, familial medullary 10.6
1883 fibrous dysplasia 10.6
1884 laryngomalacia 10.6
1885 paralytic poliomyelitis 10.6
1886 phimosis 10.6
1887 varicocele 10.6
1888 autosomal dominant polycystic kidney disease 10.6
1889 polymicrogyria with or without vascular-type ehlers-danlos syndrome 10.6
1890 gynecomastia 10.6
1891 candida glabrata 10.6
1892 adult syndrome 10.6
1893 diamond-blackfan anemia 1 10.6
1894 leri-weill dyschondrosteosis 10.6
1895 waardenburg syndrome, type 1 10.6
1896 mandibuloacral dysplasia with type a lipodystrophy 10.6
1897 mucopolysaccharidosis, type iva 10.6
1898 allan-herndon-dudley syndrome 10.6
1899 linear skin defects with multiple congenital anomalies 1 10.6
1900 loose anagen hair syndrome 10.6
1901 cataract 9, multiple types 10.6
1902 spinal muscular atrophy, distal, autosomal recessive, 1 10.6
1903 pierson syndrome 10.6
1904 dystonia, dopa-responsive, due to sepiapterin reductase deficiency 10.6
1905 hyperproinsulinemia 10.6
1906 vitelliform macular dystrophy 10.6
1907 ovarian sex-cord stromal tumor 10.6
1908 unverricht-lundborg syndrome 10.6
1909 7q11.23 duplication syndrome 10.6
1910 hoyeraal hreidarsson syndrome 10.6
1911 littoral cell angioma of the spleen 10.6
1912 paroxysmal choreoathetosis 10.6
1913 bone giant cell tumor 10.6
1914 rapidly progressive glomerulonephritis 10.6
1915 yaws 10.6
1916 thyrotoxic periodic paralysis 10.6
1917 triploidy 10.6
1918 ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive 10.6
1919 glucocorticoid-induced osteoporosis 10.6
1920 ochronosis 10.6
1921 bardet-biedl syndrome 10.6
1922 burning mouth syndrome 10.6
1923 autonomic neuropathy 10.6
1924 thyroid gland disease 10.6
1925 stickler syndrome, type i 10.6
1926 lynch syndrome i 10.6
1927 sprengel deformity 10.6
1928 ullrich congenital muscular dystrophy 1 10.6
1929 osteogenesis imperfecta, type iii 10.6
1930 neuronal intranuclear inclusion disease 10.6
1931 hurler-scheie syndrome 10.6
1932 corneal dystrophy, avellino type 10.6
1933 purine nucleoside phosphorylase deficiency 10.6
1934 chromosome 3pter-p25 deletion syndrome 10.6
1935 complement component 9 deficiency 10.6
1936 caroli disease 10.6
1937 hypochondrogenesis 10.6
1938 mast-cell sarcoma 10.6
1939 omsk hemorrhagic fever 10.6
1940 ataxia with vitamin e deficiency 10.6
1941 autoimmune progesterone dermatitis 10.6
1942 familial lcat deficiency 10.6
1943 pelizaeus-merzbacher-like disease 10.6
1944 hydrocephalus due to congenital stenosis of aqueduct of sylvius 10.6
1945 paragonimiasis 10.6
1946 mesangial proliferative glomerulonephritis 10.6
1947 keloid disorder 10.6
1948 scott syndrome 10.6
1949 transient global amnesia 10.6
1950 vulvovaginal candidiasis 10.6
1951 torticollis 10.6
1952 agoraphobia 10.6
1953 heart block, congenital 10.6
1954 microcephaly, epilepsy, and diabetes syndrome 10.6
1955 mollaret meningitis 10.6
1956 osteochondrosis 10.6
1957 hyperekplexia 1 10.6
1958 lymphatic malformation 1 10.6
1959 sneddon syndrome 10.6
1960 uncombable hair syndrome 1 10.6
1961 microphthalmia, syndromic 3 10.6
1962 coloboma, ocular, autosomal recessive 10.6
1963 glycogen storage disease ib 10.6
1964 methemoglobinemia due to deficiency of methemoglobin reductase 10.6
1965 senior-loken syndrome 1 10.6
1966 reticular dysgenesis 10.6
1967 sulfite oxidase deficiency, isolated 10.6
1968 fg syndrome 4 10.6
1969 ifap syndrome with or without bresheck syndrome 10.6
1970 cholestasis, progressive familial intrahepatic, 2 10.6
1971 bosma arhinia microphthalmia syndrome 10.6
1972 pyogenic sterile arthritis, pyoderma gangrenosum, and acne 10.6
1973 neuropathy, hereditary sensory and autonomic, type v 10.6
1974 myd88 deficiency 10.6
1975 occult macular dystrophy 10.6
1976 schuurs-hoeijmakers syndrome 10.6
1977 serine deficiency 10.6
1978 peeling skin syndrome 10.6
1979 bagassosis 10.6
1980 autosomal dominant leukodystrophy with autonomic disease 10.6
1981 endometritis 10.6
1982 tooth disease 10.6
1983 molluscum contagiosum 10.6
1984 coronary artery aneurysm 10.6
1985 neonatal diabetes mellitus 10.6
1986 neonatal meningitis 10.6
1987 methemoglobinemia 10.6
1988 syringomyelia, noncommunicating isolated 10.6
1989 sideroblastic anemia 10.6
1990 myxozoa 10.6
1991 clubfoot 10.6
1992 bronchiolitis obliterans 10.6
1993 amebiasis 10.6
1994 phobia, specific 10.6
1995 cryptogenic organizing pneumonia 10.6
1996 macrocytic anemia 10.6
1997 gastroschisis 10.6
1998 giardiasis 10.6
1999 rosacea 10.6
2000 chiari malformation type ii 10.6
2001 cavitary optic disc anomalies 10.6
2002 periodontal ehlers-danlos syndrome 10.6
2003 adie pupil 10.6
2004 brachydactyly, type b1 10.6
2005 cataract 1, multiple types 10.6
2006 hyperlipoproteinemia, type v 10.6
2007 roussy-levy hereditary areflexic dystasia 10.6
2008 gillespie syndrome 10.6
2009 atrichia with papular lesions 10.6
2010 achromatopsia 2 10.6
2011 agenesis of the corpus callosum with peripheral neuropathy 10.6
2012 baller-gerold syndrome 10.6
2013 cleft lip/palate-ectodermal dysplasia syndrome 10.6
2014 paget disease of bone 5, juvenile-onset 10.6
2015 ichthyosis, congenital, autosomal recessive 1 10.6
2016 laurence-moon syndrome 10.6
2017 mucolipidosis iii alpha/beta 10.6
2018 raine syndrome 10.6
2019 hyperoxaluria, primary, type ii 10.6
2020 renal tubular acidosis, distal, with progressive nerve deafness 10.6
2021 short syndrome 10.6
2022 peeling skin syndrome 1 10.6
2023 spermatogenic failure 4 10.6
2024 aland island eye disease 10.6
2025 nance-horan syndrome 10.6
2026 otopalatodigital syndrome, type ii 10.6
2027 epileptic encephalopathy, early infantile, 1 10.6
2028 microphthalmia, syndromic 1 10.6
2029 arthrogryposis, distal, type 2b1 10.6
2030 glomerulopathy with fibronectin deposits 2 10.6
2031 spinocerebellar ataxia 13 10.6
2032 cardiomyopathy, dilated, with woolly hair and keratoderma 10.6
2033 acute hemorrhagic leukoencephalitis 10.6
2034 emanuel syndrome 10.6
2035 spinocerebellar ataxia 28 10.6
2036 choreoathetosis and congenital hypothyroidism with or without pulmonary dysfunction 10.6
2037 ras-associated autoimmune leukoproliferative disorder 10.6
2038 night blindness, congenital stationary, type 1e 10.6
2039 simultanagnosia 10.6
2040 benign familial infantile epilepsy 10.6
2041 galloway-mowat syndrome 10.6
2042 mikulicz disease 10.6
2043 benign neonatal seizures 10.6
2044 eyelid disease 10.6
2045 48, xxxx 10.6
2046 metastatic insulinoma 10.6
2047 myh-associated polyposis 10.6
2048 waardenburg syndrome type 4 10.6
2049 colorectal adenoma 10.6
2050 myiasis 10.6
2051 polyarteritis nodosa 10.6
2052 glucagonoma 10.6
2053 breast fibroadenoma 10.6
2054 endometrial adenocarcinoma 10.6
2055 trichinosis 10.6
2056 rhabdoid tumor predisposition syndrome 1 10.6
2057 alexithymia 10.6
2058 rhabdoid cancer 10.6
2059 cerebral cavernous malformations 10.6
2060 abdominal obesity-metabolic syndrome 1 10.6
2061 hepatopulmonary syndrome 10.6
2062 fetal alcohol syndrome 10.6
2063 bruxism 10.6
2064 miliary tuberculosis 10.6
2065 human granulocytic anaplasmosis 10.6
2066 nominal aphasia 10.6
2067 pituitary gland disease 10.6
2068 interstitial cystitis 10.6
2069 craniopharyngioma 10.6
2070 penicilliosis 10.6
2071 chronic progressive external ophthalmoplegia 10.6
2072 miller fisher syndrome 10.6
2073 anemia, congenital dyserythropoietic, type iii 10.6
2074 vohwinkel syndrome 10.6
2075 dentin dysplasia, type i 10.6
2076 doyne honeycomb retinal dystrophy 10.6
2077 ectopia lentis 1, isolated, autosomal dominant 10.6
2078 hypertrichosis, congenital generalized, with or without gingival hyperplasia 10.6
2079 adermatoglyphia 10.6
2080 sorsby fundus dystrophy 10.6
2081 hematuria, benign familial 10.6
2082 keratitis-ichthyosis-deafness syndrome, autosomal dominant 10.6
2083 maxillonasal dysplasia, binder type 10.6
2084 microcoria, congenital 10.6
2085 mirror movements 1 10.6
2086 ceroid lipofuscinosis, neuronal, 4b, autosomal dominant 10.6
2087 oculopharyngodistal myopathy 1 10.6
2088 inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 1 10.6
2089 chondrodysplasia, grebe type 10.6
2090 greenberg dysplasia 10.6
2091 gm1-gangliosidosis, type iii 10.6
2092 gaucher disease, type iii 10.6
2093 hypoparathyroidism-retardation-dysmorphism syndrome 10.6
2094 3-hydroxyisobutyryl-coa hydrolase deficiency 10.6
2095 homocystinuria-megaloblastic anemia, cblg complementation type 10.6
2096 mitochondrial complex ii deficiency 10.6
2097 epilepsy, progressive myoclonic, 4, with or without renal failure 10.6
2098 mitochondrial dna depletion syndrome 6 10.6
2099 erythrocytosis, familial, 2, autosomal recessive 10.6
2100 lipodystrophy, congenital generalized, type 2 10.6
2101 spastic paraplegia 20, autosomal recessive 10.6
2102 tyrosinemia, type iii 10.6
2103 usher syndrome, type iiia 10.6
2104 xeroderma pigmentosum, complementation group f 10.6
2105 coloboma, congenital heart disease, ichthyosiform dermatosis, mental retardation, and ear anomalies syndrome 10.6
2106 epileptic encephalopathy, early infantile, 9 10.6
2107 ck syndrome 10.6
2108 immunodeficiency, x-linked, with magnesium defect, epstein-barr virus infection, and neoplasia 10.6
2109 amelogenesis imperfecta, type ie 10.6
2110 borjeson-forssman-lehmann syndrome 10.6
2111 retinitis pigmentosa 2 10.6
2112 microtia-anotia 10.6
2113 quebec platelet disorder 10.6
2114 corneal dystrophy, thiel-behnke type 10.6
2115 myopathy, myofibrillar, 9, with early respiratory failure 10.6
2116 ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 10.6
2117 spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2 10.6
2118 immunodeficiency with hyper-igm, type 3 10.6
2119 spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1 10.6
2120 hermansky-pudlak syndrome 2 10.6
2121 chromosome 3q29 deletion syndrome 10.6
2122 osteogenesis imperfecta, type vii 10.6
2123 crouzon syndrome with acanthosis nigricans 10.6
2124 microcephaly, seizures, and developmental delay 10.6
2125 hepatic lipase deficiency 10.6
2126 acth-independent macronodular adrenal hyperplasia 2 10.6
2127 chronic atrial and intestinal dysrhythmia 10.6
2128 siddiqi syndrome 10.6
2129 cold-induced sweating syndrome 10.6
2130 familial isolated hypoparathyroidism 10.6
2131 skin angiosarcoma 10.6
2132 singleton-merten syndrome 10.6
2133 deep brain stimulation for movement disorders 10.6
2134 aortic valve disease 2 10.6
2135 ossification of the posterior longitudinal ligament of spine 10.6
2136 neutrophilic dermatosis, acute febrile 10.6
2137 central neurocytoma 10.6
2138 prosopagnosia 10.6
2139 congenitally corrected transposition of the great arteries 10.6
2140 mast cell activation syndrome 10.6
2141 pituitary stalk interruption syndrome 10.6
2142 cauda equina syndrome 10.6
2143 acute kidney tubular necrosis 10.6
2144 papilledema 10.6
2145 intervertebral disc disease 10.6
2146 chromosome 16p13.3 deletion syndrome, proximal 10.6
2147 cytomegalovirus retinitis 10.6
2148 depersonalization disorder 10.6
2149 sporotrichosis 10.6
2150 transverse myelitis 10.6
2151 muir-torre syndrome 10.6
2152 myopathy, congenital 10.6
2153 wernicke-korsakoff syndrome 10.6
2154 secretory diarrhea 10.6
2155 capillary leak syndrome 10.6
2156 epidermolysis bullosa simplex 10.6
2157 recurrent respiratory papillomatosis 10.6
2158 facial cleft 10.6
2159 spondylosis 10.6
2160 chorioretinitis 10.6
2161 budd-chiari syndrome 10.6
2162 lipomatosis 10.6
2163 buerger disease 10.6
2164 lymphocytic colitis 10.6
2165 pleural tuberculosis 10.6
2166 tolosa-hunt syndrome 10.6
2167 ciguatera fish poisoning 10.6
2168 dysphagia lusoria 10.6
2169 renal hypodysplasia/aplasia 1 10.6
2170 angioma serpiginosum, autosomal dominant 10.6
2171 hypertension and brachydactyly syndrome 10.6
2172 brachydactyly, type a3 10.6
2173 osebold-remondini syndrome 10.6
2174 coloboma, ocular, autosomal dominant 10.6
2175 deafness, congenital, with onychodystrophy, autosomal dominant 10.6
2176 vibratory urticaria 10.6
2177 basan syndrome 10.6
2178 floating-harbor syndrome 10.6
2179 wagner vitreoretinopathy 10.6
2180 ichthyosis hystrix gravior 10.6
2181 keratolytic winter erythema 10.6
2182 palmoplantar keratoderma, punctate type ia 10.6
2183 bart-pumphrey syndrome 10.6
2184 cleft, median, of upper lip with polyps of facial skin and nasal mucosa 10.6
2185 metachondromatosis 10.6
2186 schilbach-rott syndrome 10.6
2187 gnathodiaphyseal dysplasia 10.6
2188 otofaciocervical syndrome 1 10.6
2189 contractures, pterygia, and spondylocarpotarsal fusion syndrome 1a 10.6
2190 overhydrated hereditary stomatocytosis 10.6
2191 bleeding disorder, platelet-type, 16 10.6
2192 nail disorder, nonsyndromic congenital, 4 10.6
2193 craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome 10.6
2194 craniometaphyseal dysplasia, autosomal recessive 10.6
2195 deafness and myopia 10.6
2196 high molecular weight kininogen deficiency 10.6
2197 gm1-gangliosidosis, type ii 10.6
2198 t-cell immunodeficiency with thymic aplasia 10.6
2199 night blindness, congenital stationary, type 1b 10.6
2200 bruck syndrome 1 10.6
2201 wiedemann-rautenstrauch syndrome 10.6
2202 hsd10 mitochondrial disease 10.6
2203 brunner syndrome 10.6
2204 trichothiodystrophy 5, nonphotosensitive 10.6
2205 wieacker-wolff syndrome 10.6
2206 spinocerebellar ataxia 5 10.6
2207 codas syndrome 10.6
2208 ichthyosis, congenital, autosomal recessive 11 10.6
2209 megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1 10.6
2210 limb-mammary syndrome 10.6
2211 ohdo syndrome, sbbys variant 10.6
2212 poikiloderma with neutropenia 10.6
2213 cerebral palsy, ataxic, autosomal recessive 10.6
2214 hemochromatosis, type 4 10.6
2215 sensory ataxic neuropathy, dysarthria, and ophthalmoparesis 10.6
2216 muscular dystrophy-dystroglycanopathy , type c, 1 10.6
2217 peeling skin syndrome 2 10.6
2218 bleeding disorder, platelet-type, 8 10.6
2219 spinocerebellar ataxia 23 10.6
2220 telangiectasia, hereditary hemorrhagic, type 4 10.6
2221 neutropenia, severe congenital, 3, autosomal recessive 10.6
2222 osteogenesis imperfecta, type xi 10.6
2223 mitochondrial complex i deficiency, nuclear type 20 10.6
2224 chromosome 15q13.3 deletion syndrome 10.6
2225 epileptic encephalopathy, early infantile, 4 10.6
2226 chromosome 1q21.1 duplication syndrome 10.6
2227 beta-ureidopropionase deficiency 10.6
2228 epileptic encephalopathy, early infantile, 7 10.6
2229 megaloblastic anemia due to dihydrofolate reductase deficiency 10.6
2230 osteogenesis imperfecta, type x 10.6
2231 osteogenesis imperfecta, type xii 10.6
2232 hydrolethalus syndrome 2 10.6
2233 stickler syndrome, type iv 10.6
2234 immunodeficiency 21 10.6
2235 cutis laxa, autosomal recessive, type iiib 10.6
2236 amyotrophic lateral sclerosis 17 10.6
2237 glucocorticoid deficiency 4 with or without mineralocorticoid deficiency 10.6
2238 ichthyosis, congenital, autosomal recessive 9 10.6
2239 osteogenesis imperfecta, type xiv 10.6
2240 osteogenesis imperfecta, type xv 10.6
2241 congenital disorder of deglycosylation 10.6
2242 macular degeneration, age-related, 13 10.6
2243 immunodeficiency 14 10.6
2244 hemochromatosis, type 5 10.6
2245 parkinson disease 20, early-onset 10.6
2246 immunodeficiency, common variable, 10 10.6
2247 myopathy with extrapyramidal signs 10.6
2248 xia-gibbs syndrome 10.6
2249 helsmoortel-van der aa syndrome 10.6
2250 spinocerebellar ataxia 37 10.6
2251 spinocerebellar ataxia 38 10.6
2252 autoinflammation with infantile enterocolitis 10.6
2253 coenzyme q10 deficiency, primary, 7 10.6
2254 mitochondrial short-chain enoyl-coa hydratase 1 deficiency 10.6
2255 immunodeficiency, common variable, 12 10.6
2256 epileptic encephalopathy, early infantile, 37 10.6
2257 polycystic liver disease 2 with or without kidney cysts 10.6
2258 deafness, autosomal dominant 34, with or without inflammation 10.6
2259 charcot-marie-tooth disease, dominant intermediate g 10.6
2260 oocyte maturation defect 6 10.6
2261 neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy 10.6
2262 phonagnosia 10.6
2263 haverhill fever 10.6
2264 carbonic anhydrase va deficiency 10.6
2265 knobloch syndrome 10.6
2266 lactate dehydrogenase deficiency 10.6
2267 mthfr gene variant 10.6
2268 pediatric autoimmune neuropsychiatric disorders associated with streptococcus infections 10.6
2269 pontocerebellar hypoplasia type 1 10.6
2270 chronic orthostatic intolerance 10.6
2271 facioscapulohumeral muscular dystrophy 1 10.6
2272 aspiration pneumonitis 10.6
2273 toxic encephalopathy 10.6
2274 muscle hypertrophy 10.6
2275 lymphoblastic lymphoma 10.6
2276 mucinous adenocarcinoma 10.6
2277 hemoglobinuria 10.6
2278 multiple chemical sensitivity 10.6
2279 nodular regenerative hyperplasia 10.6
2280 tracheobronchomalacia 10.6
2281 trachoma 10.6
2282 leukocyte adhesion deficiency, type i 10.6
2283 spinocerebellar ataxia 1 10.6
2284 polycystic kidney disease 1 with or without polycystic liver disease 10.6
2285 constricting bands, congenital 10.6
2286 twin-to-twin transfusion syndrome 10.6
2287 recessive dystrophic epidermolysis bullosa 10.6
2288 spindle cell lipoma 10.6
2289 evans' syndrome 10.6
2290 myalgic encephalomyelitis/chronic fatigue syndrome 10.6
2291 streptococcal group a invasive disease 10.6
2292 persistent vegetative state 10.6
2293 gilles de la tourette syndrome 10.6
2294 paracoccidioidomycosis 10.6
2295 cystadenocarcinoma 10.6
2296 charcot-marie-tooth disease, demyelinating, type 1a 10.6
2297 erythermalgia, primary 10.6
2298 wolf-hirschhorn syndrome 10.6
2299 junctional epidermolysis bullosa 10.6
2300 bladder disease 10.6
2301 pericoronitis 10.6
2302 dentinogenesis imperfecta