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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
1601	primary congenital glaucoma
1602	currarino syndrome
1603	lipoprotein glomerulopathy
1604	thiamine-responsive megaloblastic anemia syndrome
1605	penile cancer
1606	juvenile paget disease
1607	nocardiosis
1608	baraitser-winter syndrome
1609	cole-carpenter syndrome
1610	neurodegeneration with brain iron accumulation
1611	infective endocarditis
1612	marshall-smith syndrome
1613	lacrimoauriculodentodigital syndrome
1614	chikungunya
1615	malonic aciduria
1616	viral meningitis
1617	myhre syndrome
1618	eosinophilic pneumonia
1619	mycetoma
1620	keratoderma hereditarium mutilans
1621	condyloma
1622	coloboma of optic nerve
1623	rheumatoid nodulosis
1624	congenital stromal corneal dystrophy
1625	manitoba oculotrichoanal syndrome
1626	occipital horn syndrome
1627	bietti crystalline corneoretinal dystrophy
1628	alveolar soft part sarcoma
1629	acral peeling skin syndrome
1630	tricho-dento-osseous syndrome
1631	cloves syndrome
1632	infantile-onset ascending hereditary spastic paralysis
1633	interdigitating dendritic cell sarcoma
1634	dicarboxylic aminoaciduria
1635	platelet storage pool deficiency
1636	watson syndrome
1637	schwartz jampel syndrome
1638	recessive dystrophic epidermolysis bullosa
1639	myoclonus-dystonia syndrome
1640	marcus gunn phenomenon
1641	chst3-related skeletal dysplasia
1642	nail disease
1643	atransferrinemia
1644	meningitis, tuberculous
1645	schinzel syndrome
1646	acrokeratosis verruciformis
1647	ataxia with isolated vitamin e deficiency
1648	coffin siris syndrome
1649	dejerine sottas disease
1650	sarcoma, synovial
1651	cholangitis, primary sclerosing
1652	epilepsy, progressive myoclonic 1a
1653	peters plus syndrome
1654	ehlers-danlos syndrome, kyphoscoliotic type
1655	ehlers-danlos syndrome, type iv
1656	hemifacial atrophy, progressive
1657	hydrops fetalis, idiopathic
1658	myelopathy, htlv-1-associated
1659	clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly
1660	waardenburg syndrome type 2
1661	chromophobe renal cell carcinoma
1662	idiopathic aplastic anemia
1663	self-healing collodion baby
1664	ivic syndrome
1665	pontocerebellar hypoplasia type 1
1666	anaplastic oligodendroglioma
1667	pulmonary blastoma
1668	shprintzen-goldberg syndrome
1669	bile duct carcinoma
1670	bothnia retinal dystrophy
1671	corneal dystrophy and perceptive deafness
1672	congenital mesoblastic nephroma
1673	giant cell glioblastoma
1674	dysembryoplastic neuroepithelial tumor
1675	kuru
1676	coach syndrome
1677	fragile x-associated tremor/ataxia syndrome
1678	scalp-ear-nipple syndrome
1679	whooping cough
1680	lymphangiectasis
1681	hereditary breast and ovarian cancer syndrome
1682	cold-induced sweating syndrome
1683	hereditary leiomyomatosis and renal cell cancer
1684	hemoglobin e disease
1685	non-functioning pituitary adenoma
1686	deafness-infertility syndrome
1687	sarcocystosis
1688	hemoglobin d disease
1689	bifid nose
1690	western equine encephalitis
1691	halo nevi
1692	testicular regression syndrome
1693	snowflake vitreoretinal degeneration
1694	intracranial arteriovenous malformation
1695	adult polyglucosan body disease
1696	kerion celsi
1697	distomatosis
1698	criss-cross heart
1699	axonal neuropathy
1700	causalgia

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