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Metadata
ID	DOID:0080518
Name	Meier-Gorlin syndrome 7
Definition	A Meier-Gorlin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CDC45 gene on chromosome 22q11. https://pubmed.ncbi.nlm.nih.gov/27374770/
Xrefs	MIM:617063
Parent Relationships	is_a Meier-Gorlin syndrome is_a autosomal recessive disease