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Metadata
ID	DOID:0080246
Name	Galloway-Mowat syndrome 4
Definition	A Galloway-Mowat syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the TP53RK gene on chromosome 20q13. https://pubmed.ncbi.nlm.nih.gov/28805828/
Xrefs	MIM:617730
Parent Relationships	is_a Galloway-Mowat syndrome is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance