8C72.0

ICD-11 MMS 2026-01

Congenital myopathy with structural abnormalities

Description

Distinct group of inherited disorders of skeletal muscles which have characteristic structural abnormalities on muscle immuno-histochemistry.

Excludes

  • http://id.who.int/icd/entity/1159616108 – Secondary myopathies
  • http://id.who.int/icd/entity/1425591047 – Myasthenia gravis or certain specified neuromuscular junction disorders

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

  • 8C72.00 – Nemaline myopathy
  • 8C72.01 – Centronuclear myopathy
  • 8C72.02 – Central core disease
  • 8C72.0Y – Other specified congenital myopathy with structural abnormalities
  • 8C72.0Z – Congenital myopathy with structural abnormalities, unspecified

Sibling codes

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

Foundation entity

Congenital myopathy with structural abnormalities – http://id.who.int/icd/entity/854289056

Allowed postcoordination axes

Part of: 8C72: Congenital myopathies › 08: Diseases of the nervous system