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ID	DOID:0061293
PURL	http://purl.obolibrary.org/obo/DOID_0061293 Copy Copied!
Name	Galloway-Mowat syndrome 10
Definition	A Galloway-Mowat syndrome characterized by onset of symptoms soon after birth that has_material_basis_in homozygous or compound heterozygous mutation in the YRDC gene on chromosome 1p34. https://pubmed.ncbi.nlm.nih.gov/34545459/
Xrefs	MIM:619609
Parent Relationships	is_a Galloway-Mowat syndrome is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance