Term Name: Meier-Gorlin syndrome 4
Synonyms:
Definition: A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CDT1 gene on chromosome 16q24.
Ontology: Human Disease [DOID:0080515]   ( DOID:0080515 )

Relationships
is a type of: autosomal recessive disease Meier-Gorlin syndrome