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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: An X-linked disease 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.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
10/17/2017
MGI 6.10
The Jackson Laboratory