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Metadata
ID	DOID:0080513
Name	Meier-Gorlin syndrome 2
Definition	A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ORC4 gene on chromosome 2q23. https://www.omim.org/entry/613800
Xrefs	MIM:613800
Parent Relationships	is_a Meier-Gorlin syndrome is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance