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Musculoskeletal Abnormalities
MeSH Descriptor Data 2025
Details
Qualifiers
MeSH Tree Structures
Concepts
MeSH Heading
Musculoskeletal Abnormalities
Tree Number(s)
C05.660
C16.131.621
Unique ID
D009139
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D009139
Annotation
general or unspecified; prefer specifics or specific organ
/abnorm
Scope Note
Congenital structural abnormalities and deformities of the musculoskeletal system.
Entry Version
MUSCULOSKELETAL ABNORM
Entry Term(s)
Abnormalities, Musculoskeletal
Previous Indexing
Musculoskeletal System/abnormalities (1966-1997)
Public MeSH Note
98
History Note
98; use explode 1971-97
Date Established
1998/01/01
Date of Entry
1999/01/01
Revision Date
1999/11/03
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)
Musculoskeletal Diseases [C05]
Bone Diseases [C05.116]
Cartilage Diseases [C05.182]
Fasciitis [C05.321]
Foot Deformities [C05.330]
Foot Diseases [C05.360]
Hand Deformities [C05.390]
Jaw Diseases [C05.500]
Joint Diseases [C05.550]
Muscular Diseases [C05.651]
Musculoskeletal Abnormalities [C05.660]
Arthrogryposis [C05.660.077]
Campomelic Dysplasia [C05.660.142]
Craniofacial Abnormalities [C05.660.207]
Developmental Dysplasia of the Hip [C05.660.297]
Funnel Chest [C05.660.386]
Gastroschisis [C05.660.417]
Klippel-Feil Syndrome [C05.660.551]
Limb Deformities, Congenital [C05.660.585]
Pectus Carinatum [C05.660.745]
Synostosis [C05.660.906]
Rheumatic Diseases [C05.799]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Abnormalities, Drug-Induced [C16.131.042]
Abnormalities, Multiple [C16.131.077]
Abnormalities, Radiation-Induced [C16.131.080]
Abnormalities, Severe Teratoid [C16.131.085]
Aicardi Syndrome [C16.131.162]
Cardiovascular Abnormalities [C16.131.240]
Chromosome Disorders [C16.131.260]
Congenital Microtia [C16.131.287]
Digestive System Abnormalities [C16.131.314]
Eye Abnormalities [C16.131.384]
Hernias, Diaphragmatic, Congenital [C16.131.433]
Lymphatic Abnormalities [C16.131.482]
Musculoskeletal Abnormalities [C16.131.621]
Arthrogryposis [C16.131.621.077]
Campomelic Dysplasia [C16.131.621.142]
Cervical Rib Syndrome [C16.131.621.174]
Craniofacial Abnormalities [C16.131.621.207]
Developmental Dysplasia of the Hip [C16.131.621.297]
Funnel Chest [C16.131.621.386]
Gastroschisis [C16.131.621.417]
Hajdu-Cheney Syndrome [C16.131.621.445]
Hip Dislocation, Congenital [C16.131.621.449]
Klippel-Feil Syndrome [C16.131.621.551]
Laryngomalacia [C16.131.621.568]
Limb Deformities, Congenital [C16.131.621.585]
Pectus Carinatum [C16.131.621.745]
Synostosis [C16.131.621.906]
Tracheobronchomalacia [C16.131.621.953]
Nervous System Malformations [C16.131.666]
Respiratory System Abnormalities [C16.131.740]
Situs Inversus [C16.131.810]
Skin Abnormalities [C16.131.831]
Stomatognathic System Abnormalities [C16.131.850]
Thyroid Dysgenesis [C16.131.894]
Urogenital Abnormalities [C16.131.939]
Expand All
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Musculoskeletal Abnormalities
Preferred
Concept UI
M0014258
Scope Note
Congenital structural abnormalities and deformities of the musculoskeletal system.
Terms
Musculoskeletal Abnormalities
Preferred Term
Term UI
T027311
Date
01/01/1999
LexicalTag
NON
ThesaurusID
NLM (1966)
Abnormalities, Musculoskeletal
Term UI
T027310
Date
02/20/1997
LexicalTag
NON
ThesaurusID
NLM (1998)
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