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
1701	afibrinogenemia
1702	ophthalmia neonatorum
1703	lethal multiple pterygium syndrome
1704	distal arthrogryposis
1705	intrahepatic cholangiocarcinoma
1706	idiopathic inflammatory myopathy
1707	severe pre-eclampsia
1708	ocular toxoplasmosis
1709	pontocerebellar hypoplasia type 4
1710	charcot-marie-tooth disease type 4b1
1711	asherman syndrome
1712	radioulnar synostosis
1713	3-hydroxy-3-methylglutaric aciduria
1714	central precocious puberty
1715	heritable pulmonary arterial hypertension
1716	hereditary sensory neuropathy
1717	pelger-huet anomaly
1718	ascites, chylous
1719	myotonia permanens
1720	mycoplasmal pneumonia
1721	acute interstitial pneumonia
1722	cervical dystonia
1723	bifid uvula
1724	acute myocarditis
1725	juvenile spinal muscular atrophy
1726	constitutional mismatch repair deficiency syndrome
1727	adult dermatomyositis
1728	inflammatory breast carcinoma
1729	laryngeal carcinoma
1730	dehydrated hereditary stomatocytosis
1731	aregenerative anemia
1732	hemorrhagic fever
1733	thymus cancer
1734	large cell carcinoma
1735	cholestasis-lymphedema syndrome
1736	acrokeratoelastoidosis
1737	beare-stevenson cutis gyrata syndrome
1738	filarial elephantiasis
1739	aorta coarctation
1740	venezuelan equine encephalitis
1741	acute graft versus host disease
1742	oral lichen planus
1743	congenital vertical talus
1744	neuroaxonal dystrophy
1745	charcot-marie-tooth disease type 2b2
1746	large granular lymphocyte leukemia
1747	cystic lymphangioma
1748	gastric mucosal hypertrophy
1749	diffuse mesangial sclerosis
1750	juvenile retinoschisis
1751	chromophil renal cell carcinoma
1752	gelatinous ascites
1753	giant congenital nevus
1754	plummer vinson syndrome
1755	bamforth syndrome
1756	glucosephosphate dehydrogenase deficiency
1757	spinocerebellar ataxia 6
1758	glycogen storage disease vi
1759	spinocerebellar ataxia 5
1760	lissencephaly 1
1761	blue cone monochromacy
1762	ornithinemia
1763	familial breast cancer
1764	exstrophy of the bladder
1765	beryllium disease
1766	cataract 7
1767	miller-dieker lissencephaly syndrome
1768	autosomal dominant hypocalcemia
1769	nanophthalmia
1770	pituitary stalk interruption syndrome
1771	atypical mole
1772	progressive non-fluent aphasia
1773	mednik syndrome
1774	episodic ataxia type 6
1775	familial prostate cancer
1776	autosomal dominant optic atrophy and cataract
1777	familial multiple lipomatosis
1778	congenital intrauterine infection-like syndrome
1779	undifferentiated pleomorphic sarcoma
1780	thyroid hormone resistance syndrome
1781	afibrinogenemia, congenital
1782	acidemia, methylmalonic
1783	anemia, blackfan diamond
1784	colorblindness, tritan
1785	balantidiasis
1786	metaphyseal chondrodysplasia, schmid type
1787	narp syndrome
1788	metaphyseal chondrodysplasia, spahr type
1789	46,xx gonadal dysgenesis
1790	behr syndrome
1791	blepharophimosis
1792	fibrosing mediastinitis
1793	pten hamartoma tumor syndrome
1794	frontal encephalocele
1795	lathosterolosis
1796	elephantiasis
1797	ichthyosis prematurity syndrome
1798	fournier gangrene
1799	lymphomatoid granulomatosis
1800	ganglioneuroblastoma

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