cerebellar diseases

Preferred Label : cerebellar diseases;

MeSH definition : Diseases that affect the structure or function of the cerebellum. Cardinal manifestations of cerebellar dysfunction include dysmetria, GAIT ATAXIA, and MUSCLE HYPOTONIA.;

MeSH synonym : disease, cerebellar; cerebellar syndrome; cerebellar disease; cerebellum diseases; cerebellar syndromes; cerebellar disorder; disease, cerebellum; cerebellar disorders; cerebellum disease; cerebellar dysfunctions; syndrome, cerebellar; cerebellar dysfunction; dysfunction, cerebellar; disorder, cerebellar;

MeSH annotation : GEN: prefer specifics; general or unspecified; prefer specifics;

Details

Origin ID

D002526;

UMLS CUI

C0007760;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Autosomal dominant cerebellar ataxia type I [ORDO Disease]
- Cerebellar disease [PASCAL descriptor]
- Cerebellar disorder NOS [MedDRA LLT]
- cerebellar disease [DO Concept]
- cerebellar disorders [MedlinePlus Topic]
CISMeF manual mappings
- Cerebellar disorder (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- CEREBELLAR SYNDROME [WHO-ART Preferred Term]
- Cerebellar deficiency syndrome (disorder) [SNOMED CT concept]
- Cerebellar syndrome [PASCAL descriptor]
- Cerebellar syndrome [MedDRA Preferred Term]
- Syndrome cerebellar [MedDRA LLT]
- cerebellar disorder [Disease (Nov.)]
- cerebellar disorder [Radlex concept]
- cerebellar syndrome, nos [SNOMED Notion]
DO Cross reference
- cerebellar disease [DO Concept]
Record concept(s)
- cerebellar diseases [MeSH concept]
Related MeSH Supplementary Concept(s)
- Agenesis of Cerebellar Vermis [MeSH Supplementary Concept]
- Stevenson-Carey syndrome [MeSH Supplementary Concept]
- arima syndrome [MeSH Supplementary Concept]
- behrens baumann dust syndrome [MeSH Supplementary Concept]
- cerebellar degeneration, subacute [MeSH Supplementary Concept]
- cerebellar granule cell hypertrophy and megalencephaly [MeSH Supplementary Concept]
- cerebellar vermis aplasia with associated features suggesting Smith-Lemli-Opitz syndrome and meckel syndrome [MeSH Supplementary Concept]
- cerebelloparenchymal disorder VI [MeSH Supplementary Concept]
- dykes markes harper syndrome [MeSH Supplementary Concept]
- dystonia with cerebellar atrophy [MeSH Supplementary Concept]
- joubert syndrome 10 [MeSH Supplementary Concept]
- joubert syndrome 2 [MeSH Supplementary Concept]
- joubert syndrome 3 [MeSH Supplementary Concept]
- joubert syndrome 4 [MeSH Supplementary Concept]
- joubert syndrome 5 [MeSH Supplementary Concept]
- joubert syndrome 6 [MeSH Supplementary Concept]
- joubert syndrome 7 [MeSH Supplementary Concept]
- joubert syndrome 8 [MeSH Supplementary Concept]
- joubert syndrome 9 [MeSH Supplementary Concept]
- pontocerebellar hypoplasia [MeSH Supplementary Concept]
- pontocerebellar hypoplasia type 2B [MeSH Supplementary Concept]
- pontocerebellar hypoplasia type 2C [MeSH Supplementary Concept]
- porencephaly cerebellar hypoplasia malformations [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- CEREBELLAR SYNDROME [WHO-ART Preferred Term]
- Cerebellar deficiency syndrome (disorder) [SNOMED CT concept]
- Cerebellar disorder (disorder) [SNOMED CT concept]
- Cerebellar disorder NOS [MedDRA LLT]
- Cerebellar syndrome [MedDRA Preferred Term]
- Syndrome cerebellar [MedDRA LLT]
- cerebellar disease [DO Concept]
- cerebellar disorder [Radlex concept]
- cerebellar disorder [Disease (Nov.)]
- cerebellar disorders [MedlinePlus Topic]
- cerebellar syndrome, nos [SNOMED Notion]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients