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Metadata
ID	DOID:0080514
Name	Meier-Gorlin syndrome 3
Definition	A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ORC6 gene on chromosome 16q11. https://www.omim.org/entry/613803
Xrefs	OMIM:613803
Parent Relationships	is_a Meier-Gorlin syndrome is_a autosomal recessive disease