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Disease Ontology Browser
nephronophthisis 2 (DOID:0111113)
Alliance: disease page
Synonyms: infantile nephronophthisis 2; NPH2; NPHP2
Alt IDs: OMIM:602088
Definition: A nephronophthisis that has_material_basis_in homozygous or compound heterozygous mutation in the INVS gene on chromosome 9q31.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
11/16/2021
MGI 6.17
The Jackson Laboratory