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DOID:0111120 - nephronophthisis 9
Disease Ontology Definition:A nephronophthisis that has_material_basis_in homozygous mutation in the NEK8 gene on chromosome 17q11.
Synonyms: NPHP9
Xenbase Genes
| MONDO:0013444 - nephronophthisis 9 |
| MIM:613824 - NEPHRONOPHTHISIS 9; NPHP9 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s):
nephronophthisis (is_a)
