Fraser syndrome 1

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Summary

Literature (0)

DOID:0111405 - Fraser syndrome 1

Disease Ontology Definition:A Fraser syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the FRAS1 gene on chromosome 4q21.21.

Synonyms: FRASRS1

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

: fras1, grip1, frem2

MIM:

MIM:219000 - FRASER SYNDROME 1; FRASRS1

MIM:219000 - FRASER SYNDROME 1; FRASRS1

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)