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ID	DOID:0061289
PURL	http://purl.obolibrary.org/obo/DOID_0061289 Copy Copied!
Name	Galloway-Mowat syndrome 6
Definition	A Galloway-Mowat syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the WDR4 gene on chromosome 21q22. https://pubmed.ncbi.nlm.nih.gov/30079490/
Xrefs	MIM:618347
Parent Relationships	is_a Galloway-Mowat syndrome is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance