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
1001	benign familial neonatal epilepsy
1002	bilateral striopallidodentate calcinosis
1003	transient global amnesia
1004	herpes simplex
1005	congenital disorders of glycosylation
1006	paramyotonia congenita
1007	intermediate uveitis
1008	osteoporosis-pseudoglioma syndrome
1009	shigellosis
1010	congenital hemolytic anemia
1011	esthesioneuroblastoma
1012	hereditary neuropathy with liability to pressure palsies
1013	choroid plexus papilloma
1014	acute liver failure
1015	osteopathia striata with cranial sclerosis
1016	congenital ichthyosiform erythroderma
1017	aarskog syndrome
1018	sertoli cell-only syndrome
1019	colorectal adenoma
1020	adams oliver syndrome
1021	atypical chronic myeloid leukemia
1022	glycerol kinase deficiency
1023	embryonal rhabdomyosarcoma
1024	l1 syndrome
1025	hypoprothrombinemia
1026	chilblain lupus
1027	autosomal recessive hypophosphatemic rickets
1028	ectodermal dysplasias
1029	acute megakaryoblastic leukemia
1030	zollinger ellison syndrome
1031	dihydrolipoamide dehydrogenase deficiency
1032	sturge weber syndrome
1033	atypical mole syndrome
1034	emery dreifuss muscular dystrophy
1035	townes brocks syndrome
1036	maroteaux lamy syndrome
1037	pelizaeus merzbacher disease
1038	peripartum cardiomyopathy
1039	angioedema
1040	hypospadias
1041	corneal dystrophies
1042	hypercholesterolemia, familial
1043	rapid-onset dystonia-parkinsonism
1044	biliary cirrhosis, primary, 1
1045	craniorachischisis
1046	periventricular nodular heterotopia
1047	primary pigmented nodular adrenocortical disease
1048	cryptogenic organizing pneumonia
1049	naxos disease
1050	complete atrioventricular canal
1051	left ventricular noncompaction
1052	porokeratosis of mibelli
1053	rhabdoid tumor
1054	colonic atresia
1055	loiasis
1056	retinal vein occlusion
1057	usher syndrome type 2
1058	congenital nystagmus
1059	generalized resistance to thyroid hormone
1060	lhermitte-duclos disease
1061	perineural cyst
1062	hemorrhagic fever with renal syndrome
1063	pituitary carcinoma
1064	anaplastic thyroid carcinoma
1065	loose anagen hair syndrome
1066	intestinal obstruction
1067	ptosis
1068	brachydactyly type a1
1069	hemoglobin c disease
1070	legionellosis
1071	muscular atrophy
1072	hyperparathyroidism-jaw tumor syndrome
1073	3-methylglutaconic aciduria
1074	invasive mole
1075	mucopolysaccharidosis iii
1076	carney-stratakis syndrome
1077	glucocorticoid resistance
1078	renal cysts and diabetes syndrome
1079	aortic valve insufficiency
1080	cednik syndrome
1081	asphyxia neonatorum
1082	fibrous dysplasia of bone
1083	intrahepatic cholestasis
1084	glutaryl-coa dehydrogenase deficiency
1085	lymphoid interstitial pneumonia
1086	classic galactosemia
1087	pontocerebellar hypoplasia type 6
1088	hyperlipoproteinemia type iii
1089	riboflavin deficiency
1090	cervical squamous cell carcinoma
1091	pars planitis
1092	neovascular glaucoma
1093	desbuquois syndrome
1094	mucopolysaccharidosis vii
1095	lambert-eaton myasthenic syndrome
1096	east syndrome
1097	megacystis-microcolon-intestinal hypoperistalsis syndrome
1098	persistent mullerian duct syndrome
1099	testicular germ cell tumor
1100	posterior uveitis

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