Blood Group--Ahonen disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials

AN MCID: BLD137 MIFTS: 16	Blood Group--Ahonen (AN) Categories: Blood diseases
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Aliases & Classifications for Blood Group--Ahonen

MalaCards integrated aliases for Blood Group--Ahonen:

Name: Blood Group--Ahonen ⁵⁶

an ⁵⁶

Classifications:

MalaCards categories:
Anatomical: Blood diseases

See all MalaCards categories (disease lists)

External Ids:

OMIM ⁵⁶ 110350

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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

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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
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

Blood Group--Ahonen (AN)

Aliases & Classifications for Blood Group--Ahonen

MalaCards integrated aliases for Blood Group--Ahonen:

Classifications:

External Ids:

Summaries for Blood Group--Ahonen

Related Diseases for Blood Group--Ahonen

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