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Disease Ontology Browser
Aarskog syndrome (DOID:6683)
Alliance: disease page
Synonyms: Aarskog-Scott syndrome; faciogenital dysplasia; Greig's syndrome
Alt IDs: OMIM:100050, ICD10CM:Q87.1, MESH:C535331, NCI:C129720, UMLS_CUI:C0175701
Definition: A syndromic X-linked intellectual disability affects a person's height, muscles, skeleton, genitals, and appearance of the face.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
12/03/2019
MGI 6.14
The Jackson Laboratory