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Summary Literature (0)
DOID:0090001 - Fraser syndrome

Disease Ontology Definition:A syndrome characterized by cryptophthalmos, syndactyly, ambiguous genitalia, laryngeal and genitourinary malformations, oral clefting, and mental retardation that has_material_basis_in homozygous or compound heterozygous mutation in the FRAS1 gene on chromosome 4q21, the FREM2 gene on chromosome 13q13, or the GRIP1 gene on chromosome 12q14.

Synonyms: cryptophthalmos with other malformations,

Xenbase Genes : fras1, grip1, frem2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009046 - Fraser syndrome

OMIM:
OMIM:219000 - FRASER SYNDROME 1; FRASRS1

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

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