Karyomegalic Interstitial Nephritis

**Semantic type:** Disease or Syndrome

**Definition:** An autosomal recessive condition causes by mutation(s) in the FAN1 gene, encoding Fanconi-associated nuclease 1. It is characterized by renal failure, interstitial fibrosis, glomerular sclerosis, and atrophic tubules.

**Synonyms:** - KIN - KMIN