Fraser syndrome 3

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Summary

Literature (0)

DOID:0111406 - Fraser syndrome 3

Disease Ontology Definition:A Fraser syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the GRIP1 gene on chromosome 12q14.3.

Synonyms: FRASRS3

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

: grip1

MIM:

MIM:617667 - FRASER SYNDROME 3; FRASRS3

MIM:617667 - FRASER SYNDROME 3; FRASRS3

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

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

Parent(s): Fraser syndrome (is_a)