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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Nervous System Malformations > Congenital Cranial Dysinnervation Disorders
Nervous System Diseases > Nervous System Malformations > Congenital Cranial Dysinnervation Disorders
Eye Diseases > Ocular Motility Disorders > Oculomotor Nerve Diseases > Congenital Cranial Dysinnervation Disorders
Nervous System Diseases > Central Nervous System Diseases > Ocular Motility Disorders > Oculomotor Nerve Diseases > Congenital Cranial Dysinnervation Disorders
Nervous System Diseases > Cranial Nerve Diseases > Ocular Motility Disorders > Oculomotor Nerve Diseases > Congenital Cranial Dysinnervation Disorders

Preferred term

Congenital Cranial Dysinnervation Disorders  

Type

  • Topical Descriptor

Broader concept

Narrower concepts

Entry terms

  • Congenital Cranial Dysinnervation Syndromes
  • Congenital Fibrosis Syndrome
  • Congenital Fibrosis Syndromes
  • Congenital Innervation Dysgenesis Syndrome

Scope note

  • Congenital neurodevelopmental diseases characterized by abnormal eye, eyelid, and facial movements. Congenital cranial dysinnervation disorders (CCDDs) are caused by abnormal innervation of CRANIAL NERVES (e.g., CNs III, IV and VI) resulting in aplasia or hypoplasia of the ocular and facial musculature involved in EYE MOVEMENTS.

History note

  • 2023

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URI

http://www.yso.fi/onto/mesh/D000093922

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