MeSH Browser

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

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

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.
Terms: Congenital Cranial Dysinnervation Disorders Preferred Term
Term UI T001117995
Date02/08/2022
LexicalTag NON
ThesaurusID NLM (2023); Congenital Fibrosis Syndromes
Term UI T001117996
Date02/08/2022
LexicalTag NON
ThesaurusID NLM (2023); Congenital Cranial Dysinnervation Syndromes
Term UI T001117997
Date02/08/2022
LexicalTag NON
ThesaurusID NLM (2023); Congenital Innervation Dysgenesis Syndrome
Term UI T001117998
Date02/08/2022
LexicalTag NON
ThesaurusID NLM (2023)

Congenital Cranial Dysinnervation Disorders MeSH Descriptor Data 2024