Term Name: Meier-Gorlin syndrome 3
Synonyms:
Definition: A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ORC6 gene on chromosome 16q11.
Ontology: Human Disease [DOID:0080514]   ( DOID:0080514 )

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