X-linked Aarskog syndrome

Summary

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, faciogenital dysplasia, Greig's syndrome

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: fgd1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0007030 - autosomal dominant Aarskog syndrome

MONDO:0007030 - autosomal dominant Aarskog syndrome

MIM:

MIM:305400 - AARSKOG-SCOTT SYNDROME; AAS

MIM:305400 - AARSKOG-SCOTT SYNDROME; AAS

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), X-linked recessive disease (is_a)