Keratoderma-Ichthyosis-Deafness Syndrome, Autosomal Recessive (KDIDAR)

KID (Keratoderma-Ichthyosis-Deafness Syndrome, Autosomal Recessive), also known as kdidar, is related to arthrogryposis, renal dysfunction, and cholestasis 1 and sensorineural hearing loss. An important gene associated with KID, Autosomal Recessive is VPS33B (VPS33B Late Endosome And Lysosome Associated). Affiliated tissues include lung and bone, and related phenotypes are sensorineural hearing impairment and ichthyosis.