| Descriptor English: | Congenital Cranial Dysinnervation Disorders | ||||||
| Descriptor Spanish: |
Trastornos Congénitos de Denervación Craneal
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| Descriptor Portuguese: | Transtornos Congênitos de Denervação Craniana | ||||||
| Descriptor French: | Troubles de dysinnervation crânienne congénitale | ||||||
| Entry term(s): |
Congenital Cranial Dysinnervation Syndromes Congenital Fibrosis Syndrome Congenital Fibrosis Syndromes Congenital Innervation Dysgenesis Syndrome |
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| Tree number(s): |
C10.292.562.700.375 C10.500.198 C11.590.436.400 C16.131.666.198 |
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| RDF Unique Identifier: | https://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. |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Previous Indexing: |
Ocular Motility Disorders (2003-2022) |
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| Public MeSH Note: | 2023 |
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| History Note: | 2023 |
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| DeCS ID: | 60205 | ||||||
| Unique ID: | D000093922 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2023/01/01 | ||||||
| Date of Entry: | 2022/07/08 | ||||||
| Revision Date: | 2022/07/08 |
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DISEASES
Eye Diseases [C11]Eye Diseases
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Congenital Cranial Dysinnervation Disorders
- Preferred
| Concept UI |
M000755105 |
| 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. |
| Preferred term | Congenital Cranial Dysinnervation Disorders |
| Entry term(s) |
Congenital Cranial Dysinnervation Syndromes Congenital Fibrosis Syndrome Congenital Fibrosis Syndromes Congenital Innervation Dysgenesis Syndrome |
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