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
1401	acute inflammatory demyelinating polyradiculoneuropathy
1402	biliary tract neoplasm
1403	endemic typhus
1404	limited scleroderma
1405	chronic graft versus host disease
1406	pulmonary arteriovenous fistulas
1407	cleft soft palate
1408	chromosome 18p deletion syndrome
1409	ditra
1410	matthew-wood syndrome
1411	anaplastic large cell lymphoma
1412	breast fibroadenoma
1413	bartter disease
1414	adult t-cell leukemia
1415	plague
1416	congenital rubella
1417	hemangioma-thrombocytopenia syndrome
1418	vulva cancer
1419	phyllode tumor
1420	glycogen storage disease ib
1421	hypoadrenalism
1422	stress cardiomyopathy
1423	gangliosidosis gm1
1424	mitochondrial complex iv deficiency
1425	charcot-marie-tooth disease type 1b
1426	febrile seizures
1427	sanfilippo syndrome type a
1428	mucopolysaccharidosis type iiib
1429	allergic angiitis
1430	bile duct cysts
1431	oral leukoplakia
1432	idiopathic avascular necrosis
1433	septooptic dysplasia
1434	congenital sucrase-isomaltase deficiency
1435	hyperalphalipoproteinemia
1436	optic atrophy 1
1437	gne myopathy
1438	spinocerebellar ataxia 7
1439	spinocerebellar ataxia 2
1440	geniculate herpes zoster
1441	fetal edema
1442	sea-blue histiocyte disease
1443	acute t cell leukemia
1444	henoch-sch?nlein purpura
1445	escobar syndrome
1446	gerstmann-straussler disease
1447	mucopolysaccharidosis is
1448	waterhouse-friderichsen syndrome
1449	atypical rett syndrome
1450	well-differentiated liposarcoma
1451	joubert syndrome with orofaciodigital defect
1452	citrullinemia type ii
1453	autosomal dominant brachyolmia
1454	syndactyly type 2
1455	irida syndrome
1456	autosomal recessive axonal neuropathy with neuromyotonia
1457	autosomal dominant popliteal pterygium syndrome
1458	neuropathy, peripheral
1459	coloboma, ocular
1460	cardiomyopathy, dilated, 3b
1461	infantile onset spinocerebellar ataxia
1462	ehlers-danlos syndrome, hypermobility type
1463	mesothelioma
1464	juvenile pilocytic astrocytoma
1465	histiocytosis
1466	histiocytic sarcoma
1467	leukemoid reaction
1468	laryngocele
1469	oculocerebrocutaneous syndrome
1470	stuve-wiedemann syndrome
1471	tumoral calcinosis
1472	iniencephaly
1473	malignant peripheral nerve sheath tumor
1474	narcolepsy without cataplexy
1475	meningococcemia
1476	geleophysic dysplasia
1477	granuloma annulare
1478	mansonelliasis
1479	mitochondrial complex i deficiency
1480	myoglobinuria
1481	cauda equina syndrome
1482	diffuse neonatal hemangiomatosis
1483	respiratory failure
1484	pleomorphic xanthoastrocytoma
1485	primary intestinal lymphangiectasia
1486	ligneous conjunctivitis
1487	hepatitis a
1488	diphyllobothriasis
1489	swyer syndrome
1490	fibronectin glomerulopathy
1491	neutrophil immunodeficiency syndrome
1492	glanders
1493	chronic eosinophilic pneumonia
1494	gigantism
1495	hyperostosis frontalis interna
1496	chondroma
1497	transient hypogammaglobulinemia of infancy
1498	chronic pain
1499	laryngomalacia
1500	viral hepatitis

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