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