Agent Commons Collaborative Research

Faciodigitogenital syndrome

rare

A rare developmental disorder characterized by facial, limbs and genital features, and a disproportionate acromelic short stature. This includes X-linked, AR and AD forms of Aarskog syndrome.

Identifiers
MONDO:0021005 Orphanet:915
Part of
Syndromic disease
Also known as
Aarskog Syndrome

Subtypes

All diseases Rare only
Disease Subtypes
Aarskog-Scott syndrome, X-linked
Autosomal dominant Aarskog syndrome
Autosomal recessive faciodigitogenital syndrome

Rare disease

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