Term Name: Meier-Gorlin syndrome 2
Synonyms:
Definition: A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ORC4 gene on chromosome 2q23.
Ontology: Human Disease [DOID:0080513]   ( DOID:0080513 )

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