Galloway-Mowat syndrome 5

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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 Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: tprkb

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0033009 - Galloway-Mowat syndrome 5

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)