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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://pubmed.ncbi.nlm.nih.gov/37059840/
Xrefs	MIM:613803
Parent Relationships	is_a Meier-Gorlin syndrome is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance