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Congenital Cranial Dysinnervation Disorders MeSH Descriptor Data 2023


MeSH Heading
Congenital Cranial Dysinnervation Disorders
Tree Number(s)
C10.292.562.700.375
C10.500.198
C11.590.436.400
C16.131.666.198
Unique ID
D000093922
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D000093922
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.
Entry Term(s)
Congenital Cranial Dysinnervation Syndromes
Congenital Fibrosis Syndromes
Congenital Innervation Dysgenesis Syndrome
Previous Indexing
Ocular Motility Disorders (2003-2022)
Public MeSH Note
2023
History Note
2023
Date Established
2023/01/01
Date of Entry
2022/07/08
Revision Date
2022/07/08
Congenital Cranial Dysinnervation Disorders Preferred
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