Term Name: Meier-Gorlin syndrome 8
Synonyms:
Definition: A Meier-Gorlin syndrome that has_material_basis_in compound heterozygous mutation in the MCM5 gene on chromosome 22q12.
Ontology: Human Disease [DOID:0080255]   ( DOID:0080255 )

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