Human genes for Meier-Gorlin syndrome 8
Meier-Gorlin syndrome 8 [DOID:0080255]
A Meier-Gorlin syndrome that has_material_basis_in compound heterozygous mutation in the MCM5 gene on chromosome 22q12.
Synonyms: MeierGorlin syndrome 8, Meier-Gorlin syndrome 8, DOID:0080255