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Summary Literature (0)
DOID:6683 - X-linked Aarskog syndrome

Disease Ontology Definition:A syndromic X-linked intellectual disability affects a person's height, muscles, skeleton, genitals, and appearance of the face.

Synonyms: Aarskog-Scott syndrome, Greig's syndrome, faciogenital dysplasia,

Xenbase Genes : fgd1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007030 - autosomal dominant Aarskog syndrome

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): Aarskog syndrome (is_a), autosomal dominant disease (is_a)