Term Name: Meier-Gorlin syndrome 6
Synonyms:
Definition: A Meier-Gorlin syndrome that has_material_basis_in heterozygous mutation in the GMNN gene on chromosome 6p22.
Ontology: Human Disease [DOID:0080517]   ( DOID:0080517 )

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