LD2H.Z

ICD-11 MMS 2026-01

Syndromic genetic deafness, unspecified

Exclusions from above levels

  • http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism

Sibling codes

  • LD2H.0 – Fraser syndrome
  • LD2H.1 – Neuropathy with hearing impairment
  • LD2H.2 – Progressive deafness with stapes fixation
  • LD2H.3 – Waardenburg-Shah syndrome
  • LD2H.4 – Usher syndrome
  • LD2H.Y – Other specified syndromic genetic deafness

Foundation entity

Syndromic genetic deafness – http://id.who.int/icd/entity/186534168

Part of: LD2H: Syndromic genetic deafness › 20: Developmental anomalies