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Echinobase
Summary Literature (0)
DOID:14711 - FG syndrome

Disease Ontology 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.

Synonyms: Keller syndrome, Opitz-Kaveggia syndrome,

Echinobase Genes :


OMIM:
MIM:305450 - opitz-kaveggia syndrome; oks

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): X-linked disease (is_a)