muscular atrophy

Preferred Label : muscular atrophy;

MeSH definition : Derangement in size and number of muscle fibers occurring with aging, reduction in blood supply, or following immobilization, prolonged weightlessness, malnutrition, and particularly in denervation.;

MeSH synonym : muscular atrophies; atrophy, muscular; atrophies, muscular; muscle atrophies; atrophy, muscle; atrophies, muscle; muscle atrophy;

MeSH hyponym : neurogenic muscular atrophy; Atrophies, Neurogenic Muscular; Atrophy, Neurogenic Muscular; Muscular Atrophies, Neurogenic; Muscular Atrophy, Neurogenic; Neurogenic Muscular Atrophies; Neurotrophic Muscular Atrophy; Atrophies, Neurotrophic Muscular; Atrophy, Neurotrophic Muscular; Muscular Atrophies, Neurotrophic; Muscular Atrophy, Neurotrophic; Neurotrophic Muscular Atrophies;

MeSH annotation : MUSCULAR ATROPHY, SPINAL is also available;

Wikipedia link : https://en.wikipedia.org/wiki/Muscle atrophy;

Details

Origin ID

D009133;

UMLS CUI

C0026846;

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)
- Denervation atrophy of muscle (disorder) [SNOMED CT concept]
- Neurogenic amyotrophy [PASCAL descriptor]
- Neurogenic muscle atrophy [HPO term]
- denervation atrophy of muscle [SNOMED Notion]
- muscle symptom/complaint nos [ICPC-2 Rubric]
- muscular atrophy [DO Concept]
- musculoskeletal disease other [ICPC-2 Rubric]
Currated CISMeF NLP mapping
- AMYOTROPHY [WHO-ART Included Term]
- Amyotrophy [PASCAL descriptor]
- Amyotrophy [MedDRA Preferred Term]
- Amyotrophy [ICD-11 More detail]
- Amyotrophy NOS [MedDRA LLT]
- Atrophic Muscular Disorder [NCIt concept]
- Atrophy muscle [MedDRA LLT]
- MUSCLE ATROPHY [WHO-ART Preferred Term]
- MUSCLE WASTING [WHO-ART Included Term]
- Muscle Atrophy [NCIt concept]
- Muscle atrophy [MedDRA Preferred Term]
- Muscle atrophy (disorder) [SNOMED CT concept]
- Skeletal muscle atrophy [HPO term]
- amyotrophia, nos [SNOMED Notion]
- muscle atrophy [GO term]
- muscle atrophy [Disease (Nov.)]
- muscle wasting [TUV Concept]
- muscle wasting [TUV Term]
DO Cross reference
- muscular atrophy [DO Concept]
HPO term
- Skeletal muscle atrophy [HPO term]
Localisation(s) d'après SNOMED CT
- muscle, skeletal [MeSH Descriptor]
Record concept(s)
- muscular atrophy [MeSH concept]
- neurogenic muscular atrophy [MeSH concept]
Related MeSH Supplementary Concept(s)
- Allan-Herndon-Dudley syndrome [MeSH Supplementary Concept]
- arnold stickler bourne syndrome [MeSH Supplementary Concept]
- facial dysmorphism with multiple malformations [MeSH Supplementary Concept]
- furukawa takagi nakao syndrome [MeSH Supplementary Concept]
- lethal congenital contractural syndrome 3 [MeSH Supplementary Concept]
- miyoshi muscular dystrophy 2 [MeSH Supplementary Concept]
- miyoshi muscular dystrophy 3 [MeSH Supplementary Concept]
- miyoshi myopathy [MeSH Supplementary Concept]
- muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus [MeSH Supplementary Concept]
- muscular atrophy, malignant neurogenic [MeSH Supplementary Concept]
- nathalie syndrome [MeSH Supplementary Concept]
- primrose syndrome [MeSH Supplementary Concept]
- thakker donnai syndrome [MeSH Supplementary Concept]
- wieacker syndrome [MeSH Supplementary Concept]
See also
- muscular disorders, atrophic [MeSH Descriptor]
See also (suggested by CISMeF)
- muscular atrophy, spinal [MeSH Descriptor]
Semantic type(s)
- Pathologic Function [UMLS semantic type]
UMLS correspondences (same concept)
- AMYOTROPHY [WHO-ART Included Term]
- Amyotrophy [MedDRA Preferred Term]
- Amyotrophy NOS [MedDRA LLT]
- Atrophy muscle [MedDRA LLT]
- MUSCLE ATROPHY [WHO-ART Preferred Term]
- MUSCLE WASTING [WHO-ART Included Term]
- Muscle Atrophy [NCIt concept]
- Muscle atrophy [MedDRA Preferred Term]
- Muscle atrophy (disorder) [SNOMED CT concept]
- Muscle wasting [MedDRA LLT]
- amyotrophia, nos [SNOMED Notion]
- muscle atrophy [Disease (Nov.)]
- muscle atrophy [GO term]
- muscle wasting [TUV Concept]
- muscle wasting [TUV Term]
- muscular atrophy [DO Concept]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients