8C70.6

ICD-11 MMS 2026-01

Congenital muscular dystrophy

Description

Congenital muscular dystrophies with central nervous system abnormalities are a heterogeneous group of autosomal recessively inherited degenerative muscle disorders associated with cerebral and cerebellar dysplasia, white matter abnormalities and ocular abnormalities in some subtypes.

Index terms

  • Congenital muscular dystrophy
  • congenital hereditary muscular dystrophy
  • congenital progressive muscular dystrophy
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  • hereditary muscular dystrophy
  • hereditary progressive muscular dystrophy
  • Congenital muscular dystrophy with central nervous system abnormalities
  • Congenital muscular dystrophy Fukuyama type
  • Congenital muscular dystrophy with central nervous system abnormalities, not elsewhere classified
  • Walker Warburg syndrome
  • HARD - [Hydrocephalus - agyria - retinal dysplasia syndrome]
  • Hydrocephalus - agyria - retinal dysplasia syndrome
  • WWS - [Walker Warburg syndrome]
  • Muscle Eye Brain disease
  • MEB - [Muscle Eye Brain disease]
  • Marinesco-Sjögren syndrome
  • Congenital muscular dystrophy type 1C, fukutin-related protein gene mutation
  • Congenital muscular dystrophy type 1D large gene mutation
  • MDC1D - [congenital muscular dystrophy 1D]
  • Congenital muscular dystrophy without central nervous system symptoms
  • Congenital muscular dystrophy without central nervous system abnormalities, not elsewhere classified
  • Merosin or laminin alpha 2 chain deficiency
  • Merosin-deficient congenital muscular dystrophy
  • Collagen VI deficiency
  • Bethlem myopathy
  • Ullrich congenital muscular dystrophy
  • UCMD - [Ullrich congenital muscular dystrophy
  • Congenital muscular dystrophy - infantile cataract - hypogonadism
  • Bassoe syndrome
  • Congenital muscular dystrophy due to lamin A/C deficiency
  • Congenital muscular dystrophy due to phosphatidylcholine biosynthesis defect
  • Congenital megaconial myopathy
  • Congenital muscular dystrophy with mitochondrial structural abnormalities
  • Congenital muscular dystrophy with integrin deficiency
  • Congenital muscular dystrophy, Paradas type
  • Rigid spine syndrome
  • Congenital muscular dystrophy type 1B
  • CMD1B - [Congenital muscular dystrophy type 1B]
  • MDC1B - [Muscular Dystrophy Type 1B]

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

Sibling codes

  • 8C70.0 – Becker muscular dystrophy
  • 8C70.1 – Duchenne muscular dystrophy
  • 8C70.2 – Emery-Dreifuss muscular dystrophy
  • 8C70.3 – Facioscapulohumeral muscular dystrophy
  • 8C70.4 – Limb-girdle muscular dystrophy
  • 8C70.5 – Scapuloperoneal muscular dystrophy
  • 8C70.Y – Other specified muscular dystrophy
  • 8C70.Z – Muscular dystrophy, unspecified

Foundation entity

Congenital muscular dystrophy – http://id.who.int/icd/entity/396687076

Allowed postcoordination axes

Part of: 8C70: Muscular dystrophy › 08: Diseases of the nervous system