8A44.3

ICD-11 MMS 2026-01

Certain specified leukodystrophies

Index terms

  • Certain specified leukodystrophies
  • CACH syndrome
  • Vanishing white matter disease
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  • Childhood ataxia with central nervous system hypomyelination
  • Congenital or early infantile CACH syndrome
  • Cree leukoencephalopathy
  • Juvenile or adult CACH syndrome
  • Ovarioleukodystrophy
  • Late infantile CACH syndrome
  • Rare leukodystrophies
  • Hypomyelination with atrophy of basal ganglia or cerebellum
  • Leukoencephalopathy with bilateral anterior temporal lobe cysts
  • Megaloencephalic leukoencephalopathy with subcortical cysts
  • Polycystic lipomembranous osteodysplasia - sclerosing leukoencephalopathy
  • Nasu-Hakola disease
  • PLOSL - [Polycystic lipomembranous osteodysplasia - sclerosing leukoencephalopathy]
  • Progressive cavitating leukoencephalopathy
  • RAVINE syndrome
  • Réunion anorexia, vomiting which is irrepressible, and neurological signs
  • Hypomyelination - hypogonadotropic hypogonadism - hypodontia
  • Adult-onset leukodystrophy with axonal spheroids
  • hereditary diffuse leukoencephalopathy with axonal spheroids

Exclusions from above levels

  • 05 – Endocrine, nutritional or metabolic diseases
  • 18 – Complications of pregnancy, childbirth and the puerperium
  • 19 – Certain conditions originating in the perinatal period
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  • 22 – Injury, poisoning or certain other consequences of external causes

Foundation children elsewhere

Sibling codes

  • 8A44.0 – Pelizaeus-Merzbacher disease
  • 8A44.1 – Adrenoleukodystrophy
  • 8A44.2 – Alexander disease
  • 8A44.4 – Krabbe disease
  • 8A44.Z – Leukodystrophies, unspecified

Foundation entity

Certain specified leukodystrophies – http://id.who.int/icd/entity/1407140179

Part of: 8A44: Leukodystrophies › 08: Diseases of the nervous system