List of rare diseases starting with E
This list of
rare diseases was originally taken from the
NIH public domain resource at
http://ord.aspensys.com/asp/diseases/diseases.asp .
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
- EAF
- Eales disease
- Ear, patella, short stature syndrome
- Earlobes thickened conductive deafness
- Early infantile autism
- Ebola virus disease
- Ebstein's anomaly
- Eccentrochondrodysplasia
- Eccrine acrospiroma
- Eclampsia
- Ecp syndrome
- Ectodermal dysplasia absent dermatoglyphics
- Ectodermal dysplasia adrenal cyst
- Ectodermal dysplasia alopecia preaxial polydactyly
- Ectodermal dysplasia anhidrotic
- Ectodermal dysplasia arthrogryposis diabetes mellitus
- Ectodermal dysplasia Bartalos type
- Ectodermal dysplasia Berlin type
- Ectodermal dysplasia blindness
- Ectodermal dysplasia ectrodactyly macular dystrophy
- Ectodermal dysplasia hypohidrotic autosomal dominant
- Ectodermal dysplasia hypohidrotic hypothyroidism ciliary diskinesia
- Ectodermal dysplasia Margarita type
- Ectodermal dysplasia mental retardation CNS malformation
- Ectodermal dysplasia mental retardation syndactyly
- Ectodermal dysplasia neurosensory deafness
- Ectodermal dysplasia osteosclerosis
- Ectodermal dysplasia tricho odonto onychial type
- Ectodermal dysplasia, hydrotic
- Ectodermal dysplasia, hypohidrotic, autosomal recessive
- Ectodermal dysplasia
- Ectodermal dysplasias
- Ectodermic dysplasia anhidrotic cleft lip
- Ectopia lentis isolated
- Ectopia pupillae
- Ectopic coarctation
- Ectopic ossification familial type
- Ectopic pregnancy
- Ectrodactyly cardiopathy dysmorphism
- Ectrodactyly cleft palate syndrome
- Ectrodactyly diaphragmatic hernia corpus callosum
- Ectrodactyly dominant form
- Ectrodactyly ectrodermal dysplasia
- Ectrodactyly polydactyly
- Ectrodactyly recessive form
- Ectrodactyly
- Ectrodactyly-ectodermal dysplasia-cleft lip/cleft palate
- Ectropion inferior cleft lip and or palate
- Edinburgh malformation syndrome
- Edwards Patton Dilly syndrome
- Edwards syndrome
- Eec syndrome without cleft lip palate
- Eec syndrome
- Eem syndrome
- Egg Hypersensitivity
- Egg shaped pupils
- Ehlers-Danlos syndrome caused by tenascin-X deficiency
- Ehlers-Danlos syndrome type 1
- Ehlers-Danlos syndrome type 2
- Ehlers-Danlos syndrome type 3
- Ehlers-Danlos syndrome type 4, autosomal dominant
- Ehlers-Danlos syndrome type 5
- Ehlers-Danlos syndrome type 6
- Ehlers-Danlos syndrome type 7A
- Ehlers-Danlos syndrome type 7B
- Ehlers-Danlos syndrome type 7C
- Ehlers-danlos syndrome with platelet dysfunction from fibronectin abnormality
- Ehlers-Danlos syndrome, arthrochalasic type
- Ehlers-Danlos syndrome, classic type
- Ehlers-Danlos syndrome, dermatosparaxis type
- Ehlers-Danlos syndrome, hypermobile type
- Ehlers-danlos syndrome, type 11
- Ehlers-Danlos syndrome
- Ehrlichiosis
- Eijkman's syndrome
- Eisenmenger syndrome
- Eisoptrophobia
- Elattoproteus in context of NF
- Elective mutism
- Electron transfer flavoprotein, deficiency of
- Electrophobia
- Elejalde syndrome
- Elephant man in context of NF
- Elephantiasis
- Elliott Ludman Teebi syndrome
- Ellis Yale Winter syndrome
- Ellis-Van Creveld syndrome
- Emerinopathy
- Emery Nelson syndrome
- Emery-Dreifuss muscular dystrophy, dominant type
- Emery-Dreifuss muscular dystrophy, X-linked
- Emery-Dreifuss muscular dystrophy
- Emetophobia
- Emphysema, congenital lobar
- Emphysema
- Emphysema-penoscrotal web-deafness-mental retardation
- Empty sella syndrome
- Enamel hypoplasia cataract hydrocephaly
- Encephalitis lethargica
- Encephalo cranio cutaneous lipomatosis
- Encephalocele anencephaly
- Encephalocele anterior
- Encephalocele frontal
- Encephalocele
- Encephalomyelitis, Myalgic
- Encephalomyelitis
- Encephalopathy intracerebral calcification retinal
- Encephalopathy progressive optic atrophy
- Encephalopathy subacute spongiform, Gerstmann-Stra
- Encephalopathy-basal ganglia-calcification
- Encephalophathy recurrent of childhood
- Encephalotrigeminal angiomatosis
- Enchondromatosis (benign)
- Enchondromatosis dwarfism deafness
- Endocardial fibroelastosis
- Endocarditis, infective
- Endocarditis
- Endocrinopathy
- Endometrial stromal sarcoma
- Endometriosis
- Endomyocardial fibroelastosis
- Endomyocardial fibrosis
- Enetophobia
- Eng Strom syndrome
- Engelhard Yatziv syndrome
- Englemann disease
- Enochlophobia
- Enolase deficiency type 1
- Enolase deficiency type 2
- Enolase deficiency type 3
- Enolase deficiency type 4
- Enolase deficiency
- Enterobiasis
- Enteropathica
- Enterovirus antenatal infection
- Envenomization by bothrops lanceolatus
- Envenomization by the Martinique lancehead viper
- Environment associated hypertension
- Eosinophilia-myalgia syndrome
- Eosinophilic cryptitis
- Eosinophilic cystitis
- Eosinophilic fasciitis
- Eosinophilic gastroenteritis
- Eosinophilic granuloma
- Eosinophilic lymphogranuloma
- Eosinophilic Pustular Folliculitis
- Eosinophilic synovitis
- Eosophobia
- Ependymoblastoma
- Ependymoma
- Epidemic encephalitis
- Epidemic encephalomyelitis
- Epidermal nevus vitamin D resistant rickets
- Epidermodysplasia verruciformis
- Epidermoid carcinoma
- Epidermolysa bullosa simplex and limb girdle muscular dystrophy
- Epidermolysis bullosa acquisita
- Epidermolysis bullosa dystrophica, Bart type
- Epidermolysis bullosa dystrophica, dominant type
- Epidermolysis bullosa herpetiformis, Dowling-Meara
- Epidermolysis bullosa intraepidermic
- Epidermolysis bullosa inversa dystrophica
- Epidermolysis bullosa simplex with anodontia, hair
- Epidermolysis bullosa simplex, Cockayne-Touraine type
- Epidermolysis bullosa simplex, Koebner type
- Epidermolysis bullosa simplex, Ogna type
- Epidermolysis bullosa, dermolytic
- Epidermolysis bullosa, generalized atrophic benign
- Epidermolysis bullosa, junctional, Herlitz-Pearson
- Epidermolysis bullosa, junctional, with pyloric atrophy
- Epidermolysis bullosa, junctional
- Epidermolysis bullosa, pretibial
- Epidermolysis bullosa
- Epidermolytic hyperkeratosis
- Epidermolytic palmoplantar keratoderma Vorner type
- Epididymitis
- Epilepsy benign neonatal dominant form
- Epilepsy benign neonatal recessive form
- Epilepsy juvenile absence
- Epilepsy mental deterioration Finnish type
- Epilepsy microcephaly skeletal dysplasia
- Epilepsy occipital calcifications
- Epilepsy progressive myoclonic type 2
- Epilepsy telangiectasia
- Epilepsy with myoclono-astatic crisis
- Epilepsy, benign occipital
- Epilepsy, myoclonic progressive familial
- Epilepsy, nocturnal, frontal lobe type
- Epilepsy, partial, familial
- Epilepsy
- Epimerase deficiency
- Epimetaphyseal dysplasia cataract
- Epimetaphyseal skeletal dysplasia
- Epiphyseal dysplasia dysmorphism camptodactyly
- Epiphyseal dysplasia hearing loss dysmorphism
- Epiphyseal dysplasia multiple
- Epiphyseal stippling syndrome osteoclastic hyperplasia
- Epiphysealis hemimelica dysplasia
- Epistaxiophobia
- Epithelial-myoepithelial carcinoma
- Epitheliopathy (APMPPE)
- Epitheliopathy, acute posterior multifocal placoid
- EPP (erythropoietic protoporphyria)
- Epstein barr virus mononucleosis
- Epstein syndrome
- Equinophobia
- Erb-Duchenne palsy
- Erdheim disease
- Erdheim-Chester syndrome
- Ereuthrophobia
- Ergophobia
- Eronen Somer Gustafsson syndrome
- Erosive pustular dermatosis of the scalp
- Erysipelas
- Erythema multiforme
- Erythermalgia
- Erythroblastopenia
- Erythroderma desquamativa of Leiner
- Erythroderma lethal congenital
- Erythrokeratodermia ataxia
- Erythrokeratodermia progressive symmetrica ichthyosis
- Erythrokeratodermia symmetrica progressiva
- Erythrokeratodermia variabilis ichthyosis
- Erythrokeratodermia variabilis, Mendes da Costa type
- Erythrokeratodermia with ataxia
- Erythrokeratolysis hiemalis ichthyosis
- Erythromelalgia
- Erythroplakia
- Erythropoietic protoporphyria
- Escher Hirt syndrome
- Esophageal atresia associated anomalies
- Esophageal atresia coloboma talipes
- Esophageal atresia
- Esophageal disorder
- Esophageal duodenal atresia abnormalities of hands
- Esophageal neoplasm
- Esophageal varices
- Esotropia
- Essential hypertension
- Essential iris atrophy
- Essential mixed cryoglobulinemia
- Essential thrombocytopenia
- Essential thrombocytosis
- Esthesioneuroblastoma
- Ethylmalonic aciduria
- Ethylmalonic adipic aciduria
- Euhidrotic ectodermal dysplasia
- Eunuchoidism familial
- Euphobia
- Evan's syndrome
- Ewing's sarcoma
- Exencephaly
- Exercise induced anaphylaxis
- Exfoliative dermatitis
- Exner syndrome
- Exogenous lipoid pneumonia
- Exomphalos-macroglossia-gigantism syndrome
- Exostoses anetodermia brachydactyly type E
- Exostoses, multiple, type 1
- Exostoses, multiple, type 2
- Exostoses, multiple, type 3
- Exostoses, multiple
- Exostoses
- Experimental allergic encephalomyelitis
- Exstrophy of the bladder
- Exstrophy of the bladder-epispadias
- Exsudative retinopathy familial, autosomal dominant
- Exsudative retinopathy familial, autosomal recessive
- Exsudative retinopathy familial, X linked, recessive
- Exsudative retinopathy, familial
- Extrapyramidal disorder
- Extrasystoles short stature hyperpigmentation microcephaly
- Eye defects arachnodactyly cardiopathy
- Eyebrows duplication syndactyly