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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 : fras1, grip1, frem2



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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): Fraser syndrome (is_a)