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Please enter a likely rare disease name and press Search, then you will gain the related annotation of the likely rare disease.

About 15942 Results.

301	sjogren-larsson syndrome
302	hemochromatosis
303	muir-torre syndrome
304	rothmund-thomson syndrome
305	niemann-pick disease type b
306	hutchinson-gilford progeria syndrome
307	vogt-koyanagi-harada disease
308	lipoid proteinosis
309	familial lipoprotein lipase deficiency
310	choreoacanthocytosis
311	patent arterial duct
312	glycogen storage disease ii
313	mast cell disease
314	supravalvar aortic stenosis
315	nasopharyngeal carcinoma
316	hansen's disease
317	chronic myelocytic leukemia
318	pyoderma gangrenosum
319	macular degeneration
320	lassa fever
321	alport syndrome
322	polymyositis
323	leiomyosarcoma
324	argininosuccinic aciduria
325	pulmonary alveolar microlithiasis
326	pachyonychia congenita
327	xeroderma pigmentosum
328	rift valley fever
329	long qt syndrome
330	muscular dystrophy
331	homocystinuria
332	dermatitis herpetiformis
333	antisocial personality disorder
334	holocarboxylase synthetase deficiency
335	legionnaires' disease
336	hypertrichosis
337	babesiosis
338	yellow nail syndrome
339	glycogen storage disease
340	turner syndrome
341	nephronophthisis
342	aceruloplasminemia
343	isovaleric acidemia
344	weaver syndrome
345	mulibrey nanism
346	cystinosis
347	dermatofibrosarcoma protuberans
348	fraser syndrome
349	maffucci syndrome
350	hartnup disease
351	progressive multifocal leukoencephalopathy
352	parathyroid carcinoma
353	galloway-mowat syndrome
354	medulloblastoma
355	whim syndrome
356	fatal familial insomnia
357	acrodysostosis
358	carnitine palmitoyltransferase ii deficiency
359	succinic semialdehyde dehydrogenase deficiency
360	craniopharyngioma
361	paraganglioma
362	hereditary elliptocytosis
363	alagille syndrome
364	hereditary angioedema
365	congenital hyperinsulinism
366	chronic mucocutaneous candidiasis
367	neurofibroma
368	aicardi syndrome
369	whipple disease
370	uveal melanoma
371	inclusion body myositis
372	fundus albipunctatus
373	sapho syndrome
374	ebstein anomaly
375	spinal muscular atrophy
376	aplastic anemia
377	leukocyte adhesion deficiency
378	erythrokeratodermia variabilis
379	oculocutaneous albinism
380	feingold syndrome
381	crest syndrome
382	leishmaniasis
383	reactive arthritis
384	hemophagocytic lymphohistiocytosis
385	progressive myoclonus epilepsy
386	porphyria
387	infantile refsum disease
388	adult onset still's disease
389	interstitial cystitis
390	pyruvate carboxylase deficiency
391	lichen sclerosus
392	glycogen storage disease type v
393	peyronie's disease
394	mucous membrane pemphigoid
395	hunter syndrome
396	dyschondrosteosis
397	tourette syndrome
398	jervell and lange-nielsen syndrome
399	cri du chat syndrome
400	arginase deficiency

Rare Disease
Scleroderma ;
Biotinidase deficiency ;
Coats disease ;
Cyclic neutropenia ;
Cystinuria