MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes

Essential thrombocythemia

ORPHA:3318Disease
Multigenic/multifactorial, Not applicable

Esthesioneuroblastoma

ORPHA:1957Disease
Not applicable

Estrogen resistance syndrome

ORPHA:785Disease
Autosomal recessive

Ethylene glycol poisoning

ORPHA:31826Disease
Not applicable

Ethylmalonic encephalopathy

ORPHA:51188Disease
Autosomal recessive

Euryblepharon

ORPHA:99172Morph.
Unknown

Euthyroid Graves orbitopathy

ORPHA:466682Disease
Not applicable

Euthyroid dysprealbuminemic hyperthyroxinemia

ORPHA:597939Disease
Autosomal dominant

Evans syndrome

ORPHA:1959Disease
Not applicable

Exercise-induced hyperinsulinism

ORPHA:165991Disease
Autosomal dominant

Exercise-induced malignant hyperthermia

ORPHA:466650Disease
Multigenic/multifactorial

Exfoliative ichthyosis

ORPHA:289586Disease
Autosomal recessive

Exostoses-anetodermia-brachydactyly type E syndrome

ORPHA:1962Malform.
Unknown

Exstrophy-epispadias complex

ORPHA:322Malform.
Multigenic/multifactorial

Extensor tendons of finger anomalies

ORPHA:3294Malform.

External auditory canal aplasia/hypoplasia

ORPHA:141074Morph.
Autosomal dominant

External auditory canal atresia-vertical talus-hypertelorism syndrome

ORPHA:3023Malform.
Autosomal dominant, Not applicable, Unknown

Extracranial carotid artery aneurysm

ORPHA:494424Morph.

Extracutaneous mastocytoma

ORPHA:66662Disease

Extragonadal germ cell tumor

ORPHA:363579Cat.

Extramammary Paget disease

ORPHA:2800Disease

Extramedullary soft tissue plasmacytoma

ORPHA:100022Clin. sub.

Extraneural perineurioma

ORPHA:100002Disease

Extranodal nasal NK/T cell lymphoma

ORPHA:86879Disease
Multigenic/multifactorial, Not applicable