Term Name: Meier-Gorlin syndrome 1
Synonyms:
Definition: A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ORC1 gene on chromosome 1p32.
Ontology: Human Disease [DOID:0080512]   ( DOID:0080512 )

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