Disease Index
9,486 diseaseserythromelalgia
Human disease
MeSH: D004916
erythropoietic protoporphyria
acute porphyria characterized by a deficiency in the enzyme ferrochelatase, leading to abnormally high levels of protoporphyrin in the tissue
MeSH: D046351
erythropoietic uroporphyria associated with myeloid malignancy
human disease
esophageal atresia
congenital disorder of digestive system
MeSH: D004933
esophageal carcinoma
esophageal cancer that has material basis in abnormally proliferating cells derives from epithelial cells
esophageal duplication cyst
esophageal malformation
human disease
esophagus adenocarcinoma
esophageal carcinoma that derives from epithelial cells of glandular origin
MeSH: C562730
esophagus squamous cell carcinoma
esophageal carcinoma that derives from epithelial squamous cells located in the esophagus
MeSH: C562729
essential fructosuria
medical condition
ICD: E74.1MeSH: C538068
essential hypertension
hypertension with no known cause, the most common type of hypertension
MeSH: D000075222
essential strabismus
human disease
essential thrombocytosis
human disease
MeSH: D013920
essential tremor
movement disorder causing involuntary tremors, especially in the hand
MeSH: D020329
esthesioneuroblastoma
rare cancer of the nasal cavity
ICD: C30.0MeSH: D018304
Estrogen insensitivity syndrome
genetic variation in which the body does not respond to estrogen
Ethylene glycol poisoning
medical condition from too much ethylene glycol
ethylmalonic encephalopathy
Human disease
MeSH: C535737
euryblepharon
euthyroid Graves orbitopathy
human disease
Evans' syndrome
Human disease
MeSH: C536380
even-plus syndrome
human disease
Ewing sarcoma
bone cancer that has material basis in neural crest cells derives from undeveloped, undifferentiated neuroectoderm
ICD: C41.9MeSH: D012512
excess breast volume or number
human disease
excretory apparatus of the lacrimal system anomaly
human disease
exercise intolerance with lactic acidosis
human disease
exercise-induced hyperinsulinism
Exercise-induced hyperinsulinism (EIHI) is a form of diazoxide-sensitive diffuse hyperinsulinism (DHI) characterized by episodes of hypoglycemia induced by exercise due to an inappropriate lactate and pyruvate sensitivity in pancreatic beta-cells
MeSH: C538376
exercise-induced malignant hyperthermia
human disease
Exfoliative ichthyosis
Autosomal recessive exfoliative ichthyosis. Ichthyosis exfoliativa
exostoses-anetodermia-brachydactyly type E syndrome
MeSH: C565034