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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
:
med12,
cask,
flna
| MONDO:0002010 - FG syndrome |
| MIM:300321 - FG SYNDROME 2; FGS2 |
| MIM:300406 - FG SYNDROME 3; FGS3 |
| MIM:300422 - FG SYNDROME 4; FGS4 |
| MIM:300581 - FG SYNDROME 5; FGS5 |
| 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