9C82.4

ICD-11 MMS 2026-01

Oculomotor apraxia

Index terms

  • Oculomotor apraxia
  • Congenital ocular motor apraxia
  • Cogan’s congenital ocular motor apraxia
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  • Saccadic palsy
  • Head thrust movement
  • Congenital ocular motor apraxia associated with other neurological signs
  • Ataxia oculomotor apraxia
  • AOA - [ataxia oculomotor apraxia]
  • Autosomal recessive ataxia with oculomotor apraxia type 1
  • AOA1 - [Autosomal recessive ataxia with oculomotor apraxia type 1]
  • Autosomal recessive ataxia with oculomotor apraxia type 2
  • AOA2 - [Autosomal recessive ataxia with oculomotor apraxia type 2]
  • Acquired ocular motor apraxia
  • Frontal type
  • Parietal type
  • Fronto-parietal type
  • Balint syndrome
  • Balint-Holmes syndrome
  • Simultoagnosia
  • Dorsal simultagnosia
  • Ventral simultagnosia
  • Spasm of fixation
  • Optic ataxia

Exclusions from above levels

  • 01 – Certain infectious or parasitic diseases
  • 05 – Endocrine, nutritional or metabolic diseases
  • 18 – Complications of pregnancy, childbirth and the puerperium
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  • 19 – Certain conditions originating in the perinatal period
  • 22 – Injury, poisoning or certain other consequences of external causes
  • 8A21.0 – Posterior cortical atrophy

Sibling codes

  • 9C82.0 – Progressive external ophthalmoplegia
  • 9C82.1 – Muscular dystrophy affecting extraocular muscle
  • 9C82.2 – Congenital cranial dysinnervation syndrome
  • 9C82.3 – Restrictive ophthalmopathy
  • 9C82.Y – Other specified disorders of extraocular muscles
  • 9C82.Z – Disorders of extraocular muscles, unspecified

Foundation entity

Oculomotor apraxia – http://id.who.int/icd/entity/855225863

Allowed postcoordination axes

Part of: 9C82: Disorders of extraocular muscles › 09: Diseases of the visual system