DISEASES

Disease-gene associations mined from literature

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