DISEASES

Disease-gene associations mined from literature

Human genes for Meier-Gorlin syndrome 1

Meier-Gorlin syndrome 1 [DOID:0080512]

A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ORC1 gene on chromosome 1p32.

Synonyms:  Meier-Gorlin syndrome 1,  DOID:0080512,  MeierGorlin syndrome 1