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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://pubmed.ncbi.nlm.nih.gov/26637980/
Xrefs	MIM:616835
Parent Relationships	is_a Meier-Gorlin syndrome is_a autosomal dominant disease