Disease Index
9,486 diseasesepithelio-exfoliative colitis-deafness syndrome
This syndrome is characterised by the association of severe congenital colitis with sensorineural deafness
epithelioid hemangioendothelioma
tumor of medium-to-large veins, composed of endothelial cells that bulge into vascular spaces
MeSH: D018323
epithelioid sarcoma
human disease
epithelioid trophoblastic tumor
Human disease
epsilon-trimethyllysine hydroxylase deficiency
human disease
Epstein syndrome
disease
MeSH: C535507
Epstein-Barr virus related carcinoma
Human disease
Epstein-Barr virus-associated gastric carcinoma
Epstein-Barr virus-associated malignant lymphoproliferative disorder
human disease
Epstein-Barr virus-associated mesenchymal tumor
human disease
Epstein-Barr virus-related tumor
human disease
Epstein–Barr virus infection
Human disease
MeSH: D020031
Epstein–Barr virus-positive DLBCL, NOS
human medical condition
Erb's palsy
medical condition
ICD: P14.0
Erdheim-Chester Disease
Erdheim-Chester disease is an extremely rare non-Langerhans cell histiocytosis characterized by excessive production and accumulation of histiocytes in multiple organs. Patients present with bone pain, diabetes insipidus, exophthalmos, and cardiovascular or pulmonary involvement. Approximately 60% of cases harbor BRAF V600E mutations. Global prevalence is estimated at fewer than 1 in 1,000,000 individuals.
ICD: C96.1MeSH: D031249
Ermine phenotype
MeSH: C535508
Eronen-Somer-Gustafsson syndrome
MeSH: C563052
erosive pustular dermatitis of the scalp
characterized by the development of painful pustules, shallow erosions, and crusting on atrophic skin that eventually result in cicatricial alopecia
eruptive collagenoma
Human disease
erythema elevatum diutinum
vasculitis characterised by red, purple, brown or yellow papules (raised spot), plaques, or nodules, found on the backs of the hands, other extensor surfaces overlying joints, and on the buttocks
MeSH: C535509
Erythema palmare hereditarium
MeSH: C565041
erythroblastopenia
human desease
erythrocyte galactose epimerase deficiency
human disease
erythrokeratoderma "en cocardes"
Erythrokeratoderma variabilis progressiva
Erythrokeratodermia
human disease
erythrokeratodermia variabilis
human disease
MeSH: D056266
erythrokeratodermia variabilis et progressiva 2
human disease
erythrokeratodermia variabilis et progressiva 3
human disease
erythrokeratodermia-cardiomyopathy syndrome
human disease