eRAM

Please enter a likely rare disease name (more than 2 characters) and press Search, then you will gain the related annotation of the likely rare disease.

About 15942 Results.

ID	Disease
1501	osteoblastoma
1502	acrogeria
1503	tremor
1504	achondrogenesis
1505	chondroblastoma
1506	zygomycosis
1507	hypokalemia
1508	transient neonatal diabetes mellitus
1509	gliosarcoma
1510	chronic eosinophilic leukemia
1511	central neurocytoma
1512	spermatocytic seminoma
1513	alveolar echinococcosis
1514	jalili syndrome
1515	cobb syndrome
1516	nevus of ota
1517	solitary fibrous tumor
1518	hymenolepiasis
1519	sirenomelia
1520	acute myelomonocytic leukemia
1521	hemosiderosis
1522	donnai-barrow syndrome
1523	choriocarcinoma
1524	brachytelephalangic chondrodysplasia punctata
1525	spondyloepimetaphyseal dysplasia with joint laxity
1526	methylmalonic acidemia with homocystinuria
1527	monostotic fibrous dysplasia
1528	rabson-mendenhall syndrome
1529	filippi syndrome
1530	acromicric dysplasia
1531	omsk hemorrhagic fever
1532	frontonasal dysplasia
1533	farmer's lung
1534	epithelioid hemangioendothelioma
1535	kufor-rakeb syndrome
1536	microsporidiosis
1537	episodic ataxia
1538	postural orthostatic tachycardia syndrome
1539	orotic aciduria
1540	mumps
1541	trimethylaminuria
1542	intraocular lymphoma
1543	porokeratotic eccrine ostial and dermal duct nevus
1544	neurofibromatosis
1545	follicular dendritic cell sarcoma
1546	idiopathic hypersomnia
1547	iminoglycinuria
1548	ainhum
1549	chondrocalcinosis
1550	actinomycosis
1551	epidermal nevus syndrome
1552	gerstmann syndrome
1553	botulism
1554	pellagra
1555	acrodermatitis
1556	rapidly progressive glomerulonephritis
1557	lymphogranuloma venereum
1558	cytomegalovirus retinitis
1559	primary central nervous system lymphoma
1560	lead poisoning
1561	severe congenital neutropenia
1562	factor xiii deficiency
1563	angiostrongyliasis
1564	scleritis
1565	central retinal vein occlusion
1566	retinitis punctata albescens
1567	haim-munk syndrome
1568	sporotrichosis
1569	annular pancreas
1570	tracheomalacia
1571	pentalogy of cantrell
1572	chorioretinitis
1573	peeling skin syndrome
1574	myelitis
1575	superior mesenteric artery syndrome
1576	epidermolysis bullosa simplex with muscular dystrophy
1577	poikiloderma with neutropenia
1578	heparin-induced thrombocytopenia
1579	adenoid cystic carcinoma
1580	ghosal hematodiaphyseal dysplasia
1581	dirofilariasis
1582	langer mesomelic dysplasia
1583	hyperekplexia
1584	hyper igd syndrome
1585	agenesis of corpus callosum
1586	x-linked alport syndrome
1587	prosopagnosia
1588	microcephalic osteodysplastic primordial dwarfism type ii
1589	h syndrome
1590	mckusick-kaufman syndrome
1591	osteochondroma
1592	complement factor h deficiency
1593	carnitine-acylcarnitine translocase deficiency
1594	capillary leak syndrome
1595	fetal valproate syndrome
1596	lethal osteosclerotic bone dysplasia
1597	infantile neuronal ceroid lipofuscinosis
1598	essential fructosuria
1599	pigmented villonodular synovitis
1600	tracheobronchomalacia

Rare Disease
Rett syndrome ;
Scleroderma ;
Coats disease ;
Cyclic neutropenia ;
Cystinuria