Kanzaki Disease, also known as alpha-n-acetylgalactosaminidase deficiency type 2, is related to schindler disease, type i and schindler disease, and has symptoms including vertigo and dry skin. An important gene associated with Kanzaki Disease is NAGA (Alpha-N-Acetylgalactosaminidase), and among its related pathways/superpathways are Metabolism and Sphingolipid metabolism. Affiliated tissues include eye and skin, and related phenotypes are intellectual disability, mild and hyperkeratosis