FG syndrome

Summary

DOID:14711 - FG syndrome

Disease Ontology 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.

Synonyms: Keller syndrome, Opitz-Kaveggia 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

: med12, cask, flna

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0002010 - FG syndrome

MONDO:0002010 - FG syndrome

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): X-linked monogenic disease (is_a), syndrome (is_a)