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GTR Home > Conditions/Phenotypes > Karyomegalic interstitial nephritis

Karyomegalic interstitial nephritis

Summary

Karyomegalic tubulointerstitial nephritis (KMIN) is a rare kidney disease characterized clinically by onset in the third decade of progressive renal failure. Renal biopsy shows chronic tubulointerstitial nephritis and interstitial fibrosis associated with enlarged and atypical tubular epithelial cell nuclei (summary by Baba et al., 2006). [from OMIM]

Available tests

27 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (27 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: KIAA1018, KMIN, MTMR15, hFAN1, FAN1
    Summary: FANCD2 and FANCI associated nuclease 1

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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