Visualize Submit Comment

Metadata
ID	DOID:0080245
Name	Galloway-Mowat syndrome 3
Definition	A Galloway-Mowat syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the OSGEP gene on chromosome 14q11. https://pubmed.ncbi.nlm.nih.gov/28805828/
Xrefs	MIM:617729
Parent Relationships	is_a Galloway-Mowat syndrome is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance