eRAM

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.

401	smith lemli opitz syndrome
402	dystonia
403	sick sinus syndrome
404	narcolepsy
405	uveitis
406	meningioma
407	nephrotic syndrome
408	antiphospholipid syndrome
409	hypothyroidism
410	hypertrophic cardiomyopathy
411	bronchopulmonary dysplasia
412	autoimmune hepatitis
413	myalgic encephalomyelitis
414	premature ovarian failure
415	thoracic aortic aneurysm
416	pilomatrixoma
417	nail-patella syndrome
418	temporal arteritis
419	muckle-wells syndrome
420	charcot-marie-tooth disease
421	localized scleroderma
422	hydatidiform mole
423	diffuse cutaneous systemic sclerosis
424	becker muscular dystrophy
425	cartilage-hair hypoplasia
426	panhypopituitarism
427	peters anomaly
428	west syndrome
429	brittle cornea syndrome
430	cutaneous mastocytoma
431	balkan nephropathy
432	schistosomiasis
433	mowat-wilson syndrome
434	langer-giedion syndrome
435	factor xii deficiency
436	cadasil
437	ewing sarcoma
438	machado-joseph disease
439	arrhythmogenic right ventricular cardiomyopathy
440	metabolic syndrome x
441	chronic myeloproliferative disease
442	nemaline myopathy
443	basal cell nevus syndrome
444	charcot-marie-tooth disease type 1a
445	familial benign chronic pemphigus
446	systemic mastocytosis
447	porphyria variegata
448	buerger disease
449	clear cell renal carcinoma
450	isolated polycystic liver disease
451	berardinelli-seip congenital lipodystrophy
452	crouzon disease
453	merrf
454	fructose intolerance
455	multiple acyl-coa dehydrogenase deficiency
456	monoclonal gammopathy of uncertain significance
457	congenital lymphedema
458	sjogren's syndrome
459	acute lymphocytic leukemia
460	sclerosing cholangitis
461	b-cell lymphomas
462	vesicoureteral reflux
463	astrocytoma
464	microscopic polyangiitis
465	kniest dysplasia
466	gray platelet syndrome
467	cockayne syndrome
468	hemolytic-uremic syndrome
469	acanthosis nigricans
470	double outlet right ventricle
471	porokeratosis
472	lissencephaly
473	achromatopsia
474	klinefelter syndrome
475	scleroderma
476	hepatoblastoma
477	boomerang dysplasia
478	microcephaly
479	paroxysmal nocturnal hemoglobinuria
480	cushing syndrome
481	rhabdomyosarcoma
482	rapadilino syndrome
483	piebaldism
484	felty syndrome
485	angioimmunoblastic t-cell lymphoma
486	fibrochondrogenesis
487	pyomyositis
488	aspartylglucosaminuria
489	pulmonary arterial hypertension
490	congenital dyserythropoietic anemia
491	waardenburg syndrome
492	tardive dyskinesia
493	myositis
494	cogan syndrome
495	complete androgen insensitivity syndrome
496	cerebral amyloid angiopathy
497	evans syndrome
498	fucosidosis
499	cohen syndrome
500	anencephaly

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