Human genes for Meier-Gorlin syndrome 4
Meier-Gorlin syndrome 4 [DOID:0080515]
A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CDT1 gene on chromosome 16q24.
Synonyms: Meier-Gorlin syndrome 4, DOID:0080515, MeierGorlin syndrome 4