8C72

ICD-11 MMS 2026-01

Congenital myopathies

Exclusions from above levels

  • http://id.who.int/icd/entity/155258022 – Metabolic disorders
  • LD26.41 – Arthrogryposis multiplex congenita
  • 05 – Endocrine, nutritional or metabolic diseases
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  • 18 – Complications of pregnancy, childbirth and the puerperium
  • 19 – Certain conditions originating in the perinatal period
  • 22 – Injury, poisoning or certain other consequences of external causes

Child codes

  • 8C72.0 – Congenital myopathy with structural abnormalities
  • 8C72.1 – Congenital myopathy with no structural abnormalities
  • 8C72.Y – Other specified congenital myopathies
  • 8C72.Z – Congenital myopathies, unspecified

Sibling codes

  • 8C70 – Muscular dystrophy
  • 8C71 – Myotonic disorders
  • 8C73 – Mitochondrial myopathies
  • 8C74 – Periodic paralyses or disorders of muscle membrane excitability
  • 8C75 – Distal myopathies
  • 8C76 – Myofibrillar myopathy
  • 8C77 – Ocular myopathy
  • 8C78 – Malignant hyperthermia or hyperpyrexia
  • 8C7Y – Other specified primary disorders of muscles
  • 8C7Z – Primary disorders of muscles, unspecified

Foundation entity

Congenital myopathies – http://id.who.int/icd/entity/1185572073

Allowed postcoordination axes

Part of: 08: Diseases of the nervous system