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Disease Ontology Browser
FG syndrome (DOID:14711)
Alliance: disease page
Synonyms: Keller syndrome; Opitz-Kaveggia syndrome
Alt IDs: OMIM:300321, OMIM:300406, OMIM:300422, OMIM:300581, OMIM:305450, MESH:C537923, ORDO:323, ORDO:93932, UMLS_CUI:C0220769
Definition: A syndrome characterized by retardation, hyperactivity, hypotonia, broad thumbs, big first toes and a characteristic facial appearance including macrocephaly and has an X-linked recessive inheritance pattern.

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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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory