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Summary Literature (0)
DOID:0111407 - Fraser syndrome 2

Disease Ontology Definition:A Fraser syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the FREM2 gene on chromosome 13q13.3.

Synonyms: FRASRS2

Xenbase Genes : frem2


MIM:
MIM:617666 - FRASER SYNDROME 2; FRASRS2

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)