nephronophthisis 3

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Summary

Literature (0)

DOID:0111114 - nephronophthisis 3

Disease Ontology Definition:A nephronophthisis that has_material_basis_in homozygous or compound heterozygous mutation in the NPHP3 gene on chromosome 3q22.

Synonyms: NPH3, NPHP3

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

: nphp3

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011456 - nephronophthisis 3

MONDO:0011456 - nephronophthisis 3

MIM:

MIM:604387 - NEPHRONOPHTHISIS 3; NPHP3

MIM:604387 - NEPHRONOPHTHISIS 3; NPHP3

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): nephronophthisis (is_a)