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Medical Subject Headings
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/MESH/D000093922
http://purl.bioontology.org/ontology/MESH/D000093922
|
|---|---|
| Preferred Name | Congenital Cranial Dysinnervation Disorders |
| Definitions |
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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| Synonyms |
Congenital Fibrosis Syndromes
Congenital Cranial Dysinnervation Syndromes
Congenital Fibrosis Syndrome
Congenital Innervation Dysgenesis Syndrome
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition | 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. |
|---|---|
| altLabel |
Congenital Fibrosis Syndromes
Congenital Cranial Dysinnervation Syndromes
Congenital Fibrosis Syndrome
Congenital Innervation Dysgenesis Syndrome
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| prefLabel | Congenital Cranial Dysinnervation Disorders
|
| Machine permutation | 2023
|
| HN | 2023
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| Mapped from |
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| type | |
| tui | T047
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| TERMUI |
T001117998
T001117996
T001117997
T001117995
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| TH | NLM (2023)
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| MMR | 20230101
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| notation | D000093922
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| Semantic type UMLS property | |
| Inverse of AQ |
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| DX | 20230101
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| cui | C5671326
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| DC | 1
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| MN |
C11.590.436.400
C10.292.562.700.375
C10.500.198
C16.131.666.198
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| AQL | BL CF CI CL CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI
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| MDA | 20220208
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| subClassOf |
| Delete | Subject | Author | Type | Created |
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| No notes to display |