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Metadata
ID	DOID:0080517
Name	Meier-Gorlin syndrome 6
Definition	A Meier-Gorlin syndrome that has_material_basis_in heterozygous mutation in the GMNN gene on chromosome 6p22. https://www.omim.org/entry/616835
Xrefs	OMIM:616835
Parent Relationships	is_a Meier-Gorlin syndrome is_a autosomal dominant disease