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
1301	15q13.3 microdeletion syndrome
1302	acth-independent cushing syndrome
1303	cone dystrophy
1304	familial male-limited precocious puberty
1305	adrenal adenoma
1306	sympathetic ophthalmia
1307	ichthyosis bullosa of siemens
1308	acromesomelic dysplasia
1309	reticulate acropigmentation of kitamura
1310	compartment syndrome
1311	membranoproliferative glomerulonephritis
1312	myeloid sarcoma
1313	jacobsen syndrome
1314	hyperphenylalaninemia
1315	atrial septal defects
1316	eec syndrome
1317	adenylosuccinate lyase deficiency
1318	mal de meleda
1319	acth deficiency
1320	christianson syndrome
1321	2-hydroxyglutaric aciduria
1322	gallbladder disease
1323	transitional cell carcinoma
1324	scleredema
1325	hand-foot-genital syndrome
1326	gangliosidosis
1327	oral cancer
1328	glycogen storage disease type vii
1329	alpers disease
1330	schnyder corneal dystrophy
1331	thrombocytopenia absent radius syndrome
1332	autosomal recessive spastic ataxia of charlevoix-saguenay
1333	mucocutaneous venous malformations
1334	tumor necrosis factor receptor-associated periodic syndrome
1335	dupuytren's contracture
1336	oculo-dento-digital dysplasia
1337	5-oxoprolinuria
1338	saethre chotzen syndrome
1339	hajdu cheney syndrome
1340	landau kleffner syndrome
1341	simpson dysmorphia syndrome
1342	crigler najjar syndrome
1343	fructose-1,6-bisphosphatase deficiency
1344	46,xx testicular disorder of sex development
1345	benign paroxysmal positional nystagmus
1346	severe combined immunodeficiency, x-linked
1347	craniofacial microsomia
1348	panencephalitis, subacute sclerosing
1349	gm2 gangliosidosis, ab variant
1350	congenital ptosis
1351	lig4 syndrome
1352	klippel-feil syndrome
1353	inflammatory myofibroblastic tumor
1354	nephrosclerosis
1355	haddad syndrome
1356	pneumococcal meningitis
1357	primary cutaneous anaplastic large cell lymphoma
1358	short rib-polydactyly syndrome
1359	penoscrotal transposition
1360	anisakiasis
1361	spasmus nutans
1362	blount disease
1363	reflex sympathetic dystrophy
1364	palmoplantar keratosis
1365	bohring-opitz syndrome
1366	t-cell large granular lymphocyte leukemia
1367	giant cell tumor of bone
1368	endomyocardial fibrosis
1369	panuveitis
1370	tricuspid valve prolapse
1371	linear iga dermatosis
1372	aggressive systemic mastocytosis
1373	primary mediastinal large b-cell lymphoma
1374	meningocele
1375	lemierre syndrome
1376	drug rash with eosinophilia and systemic symptoms
1377	gangliocytoma
1378	lyell syndrome
1379	gnathodiaphyseal dysplasia
1380	kimura disease
1381	palatopharyngeal incompetence
1382	night blindness
1383	maternal phenylketonuria
1384	thymic tumor
1385	trichinellosis
1386	tracheal stenosis
1387	autosomal dominant emery-dreifuss muscular dystrophy
1388	thalidomide embryopathy
1389	warsaw breakage syndrome
1390	amebiasis
1391	autosomal recessive hypohidrotic ectodermal dysplasia
1392	fibrous dysplasia
1393	sengers syndrome
1394	otopalatodigital syndrome
1395	dyggve-melchior-clausen disease
1396	familial hemophagocytic lymphohistiocytosis
1397	peripheral t-cell lymphoma
1398	sheehan syndrome
1399	miller fisher syndrome
1400	yolk sac tumor

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