Human genes for Fraser syndrome
Fraser syndrome [DOID:0090001]
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: Fraser syndrome, DOID:0090001, Fraser disease, Fraser disorder, Fraser syndromes ...