Visualize Submit Comment

Metadata
ID	DOID:0061292
PURL	http://purl.obolibrary.org/obo/DOID_0061292 Copy Copied!
Name	Galloway-Mowat syndrome 9
Definition	A Galloway-Mowat syndrome characterized by onset of nephrotic syndrome with proteinuria in infancy or early childhood that has_material_basis_in homozygous mutation in the GON7 gene on chromosome 14q32. https://pubmed.ncbi.nlm.nih.gov/31481669/
Xrefs	MIM:619603
Parent Relationships	is_a Galloway-Mowat syndrome is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance