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Summary Literature (0)
DOID:0080247 - Galloway-Mowat syndrome 5


Disease Ontology Definition:A Galloway-Mowat syndrome that has_material_basis_in homozygous mutation in the TPRKB gene on chromosome 2p13.

Synonyms:

Xenbase Genes : tprkb

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0033009 - Galloway-Mowat syndrome 5


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): Galloway-Mowat syndrome (is_a)