FG syndrome

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Echinobase

Summary

Literature (0)

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

Echinobase 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

MIM:

MIM:305450 - opitz-kaveggia syndrome; oks

MIM:305450 - opitz-kaveggia syndrome; oks

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

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

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