nephronophthisis 12 Disease Ontology Browser

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Disease Ontology Browser

nephronophthisis 12 (DOID:0111119)
Alliance: disease page
Synonyms: NPHP12
Alt IDs: OMIM:613820
Definition: A nephronophthisis that has_material_basis_in homozygous or compound heterozygous mutation in the TTC21B gene on chromosome 2q24.

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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