8C72.1

ICD-11 MMS 2026-01

Congenital myopathy with no structural abnormalities

Index terms

  • Congenital myopathy with no structural abnormalities
  • Congenital fibre type disproportion
  • congenital myopathy with fiber type disproportion
Show allHide
  • congenital myopathy with fibre type disproportion
  • fiber-type disproportion
  • fibre-type disproportion
  • Congenital myopathy with no specific features or minimal change
  • minimal change myopathy
  • Congenital myopathy with muscle fibre immaturity
  • Congenital neuromuscular disorder with uniform type 1 fibre
  • Congenital myopathy with type 1 fibre predominance
  • Myosclerosis

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
Show allHide
  • 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

Sibling codes

  • 8C72.0 – Congenital myopathy with structural abnormalities
  • 8C72.Y – Other specified congenital myopathies
  • 8C72.Z – Congenital myopathies, unspecified

Foundation entity

Congenital myopathy with no structural abnormalities – http://id.who.int/icd/entity/514523225

Allowed postcoordination axes

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