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Myopathy (CUI C0026848) Suggest changes to this concept
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Terms & Properties

Concept Unique Identifier (CUI): C0026848

NCI Thesaurus Code: C101216  (see NCI Thesaurus info)

Semantic Type: Disease or Syndrome

NCIt Definition: A non-neoplastic disorder that affects the muscles. Representative examples include muscular dystrophy, metabolic myopathies, muscular atrophies, and dermatomyositis.

HPO Definition: A disorder of muscle unrelated to impairment of innervation or neuromuscular junction. [HPO:probinson]

MEDLINEPLUS Definition: 

Your muscles help you move and help your body work. Different types of muscles have different jobs. There are many problems that can affect muscles. Muscle disorders can cause weakness, pain or even paralysis.

Causes of muscle disorders include

Sometimes the cause is not known.

CSP Definition: impairment of health or a condition of abnormal functioning of the muscle.

MSH Definition: Acquired, familial, and congenital disorders of SKELETAL MUSCLE and SMOOTH MUSCLE.

Synonyms & Abbreviations: (see Synonym Details)
Disease of skeletal muscle
DISORDER MUSCLE
Disorder of muscle, unspecified
Disorder of muscle
Disorder of skeletal AND/OR smooth muscle (disorder)
Disorder of skeletal AND/OR smooth muscle
Disorder of skeletal muscle (disorder)
Disorder of skeletal muscle
Disorders of muscles (M60-M63)
Disorders of muscles
Muscle disorder NOS
Muscle disorders
muscle disorder
MUSCLE DIS
Muscle tissue disease
Muscular Diseases [Disease/Finding]
Muscular Diseases
Muscular Disease
Muscular Disorders
muscular disorder
MUSCULAR DIS
Myopathic changes
Myopathic Conditions
Myopathic Condition
Myopathic disease
Myopathies
Myopathy NOS
Myopathy, unspecified
myopathy

External Source Codes: 
NCI Thesaurus Code C101216 (see NCI Thesaurus info)

Other Properties: Property Definitions
Name Value Source
ACTIVE 1 SNOMEDCT_US
AN GEN; prefer specifics; inflamm dis = MYOSITIS. /congen: consider also Myopathies, Structural, Congenital & its indentions MSH
AQL BL CF CI CL CN 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 MSH
CASE_SIGNIFICANCE_ID 900000000000020002 SNOMEDCT_US
CASE_SIGNIFICANCE_ID 900000000000448009 SNOMEDCT_US
Contributing_Source NICHD NCI
CTV3ID X708D SNOMEDCT_US
CTV3ID XUPpE SNOMEDCT_US
DATE_CREATED 08/19/2014 RADLEX
DATE_CREATED 11/03/1999 MEDLINEPLUS
DATE_LAST_MODIFIED 3.12 RADLEX
DC 1 MSH
DEFINITION_STATUS_ID 900000000000073002 SNOMEDCT_US
DID 1982-9451 CSP
DX 19660101 MSH
EFFECTIVE_TIME 20020131 SNOMEDCT_US
EXCLUDES1 dermatopolymyositis (M33.-) ICD10CM
EXCLUDES1 muscular dystrophies and myopathies (G71-G72) ICD10CM
EXCLUDES1 myopathy in amyloidosis (E85.-) ICD10CM
EXCLUDES1 myopathy in polyarteritis nodosa (M30.0) ICD10CM
EXCLUDES1 myopathy in rheumatoid arthritis (M05.32) ICD10CM
EXCLUDES1 myopathy in scleroderma (M34.-) ICD10CM
EXCLUDES1 myopathy in Sjögren's syndrome (M35.03) ICD10CM
EXCLUDES1 myopathy in systemic lupus erythematosus (M32.-) ICD10CM
HPO_COMMENT The diagnosis of myopathy is often confirmed on the basis of myopathic changes in muscle biopsy. HPO
IAN DEFAULT ICD10
LAST_CHANGES_TO_CLASS new RADLEX
MDA 19990101 MSH
MESH_DEFINITION Acquired, familial, and congenital disorders of SKELETAL MUSCLE and SMOOTH MUSCLE. NDFRT
MESH_DUI D009135 NDFRT
MESH_NAME Muscular Diseases NDFRT
MESH_UI M0014252 NDFRT
MMR 20080708 MSH
MN C05.651 MSH
MN C10.668.491 MSH
MP_HEALTH_TOPIC_URL https://www.nlm.nih.gov/medlineplus/muscledisorders.html MEDLINEPLUS
MP_OTHER_LANGUAGE_URL Somali https://www.nlm.nih.gov/medlineplus/languages/muscledisorders.html#Somali MEDLINEPLUS
MP_OTHER_LANGUAGE_URL Spanish https://www.nlm.nih.gov/medlineplus/spanish/muscledisorders.html MEDLINEPLUS
MP_PRIMARY_INSTITUTE_URL National Institute of Arthritis and Musculoskeletal and Skin Diseases http://www.niams.nih.gov/ MEDLINEPLUS
NDFRT_KIND DISEASE_KIND NDFRT
NICHD_Hierarchy_Term Myopathy NCI
NUI N0000002064 NDFRT
ORDER_NO 06384 ICD10CM
ORDER_NO 19163 ICD10CM
PRIMARY_PATH 10028300$10028326$10028302$10028395$Muscle disorder$Muscle related signs and symptoms NEC$Muscle disorders$Musculoskeletal and connective tissue disorders MDR
PRIMARY_PATH 10028641$10028640$10028302$10028395$Myopathy$Myopathies$Muscle disorders$Musculoskeletal and connective tissue disorders MDR
PRIMARY_SOC 10028395 MDR
PT_IN_VERSION 10.0 MDR
PT_IN_VERSION 10.1 MDR
PT_IN_VERSION 11.0 MDR
PT_IN_VERSION 11.1 MDR
PT_IN_VERSION 12.0 MDR
PT_IN_VERSION 12.1 MDR
PT_IN_VERSION 13.0 MDR
PT_IN_VERSION 13.1 MDR
PT_IN_VERSION 14.0 MDR
PT_IN_VERSION 14.1 MDR
PT_IN_VERSION 15.0 MDR
PT_IN_VERSION 15.1 MDR
PT_IN_VERSION 16.0 MDR
PT_IN_VERSION 16.1 MDR
PT_IN_VERSION 17.0 MDR
PT_IN_VERSION 17.1 MDR
PT_IN_VERSION 18.0 MDR
PT_IN_VERSION 18.1 MDR
PT_IN_VERSION 19.0 MDR
PT_IN_VERSION 19.1 MDR
PT_IN_VERSION 20.0 MDR
PT_IN_VERSION 20.1 MDR
PT_IN_VERSION 8.0 MDR
PT_IN_VERSION 8.1 MDR
PT_IN_VERSION 9.0 MDR
PT_IN_VERSION 9.1 MDR
REF orcid.org/0000-0001-5208-3432 HPO
RXAUI 3200259 RXNORM
RXAUI 3200350 RXNORM
RXAUI 3200351 RXNORM
RXAUI 3200936 RXNORM
RXAUI 3200942 RXNORM
RXCUI 1022424 RXNORM
SID HP:0003569 HPO
SID HP:0003705 HPO
SID HP:0003742 HPO
SID HP:0003802 HPO
SMQ_TERM_ADDVERSION 19.0 MDR
SMQ_TERM_ADDVERSION 7.1 MDR
SMQ_TERM_CAT A MDR
SMQ_TERM_CAT B MDR
SMQ_TERM_LEVEL 4 MDR
SMQ_TERM_LEVEL 5 MDR
SMQ_TERM_LMVERSION 19.0 MDR
SMQ_TERM_LMVERSION 7.1 MDR
SMQ_TERM_SCOPE 1 MDR
SMQ_TERM_SCOPE 2 MDR
SMQ_TERM_STATUS A MDR
SMQ_TERM_WEIGHT 0 MDR
SNOMED_CID 129565002 NDFRT
SUBSET_MEMBER 447562003~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPADVICE~ALWAYS M62.99 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPCATEGORYID~447637006 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPGROUP~1 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPPRIORITY~1 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPRULE~TRUE SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPTARGET~M62.99 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~ALWAYS M62.9 | DESCENDANTS NOT EXHAUSTIVELY MAPPED SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~IF AGE AT ONSET OF CLINICAL FINDING BEFORE 29.0 DAYS CHOOSE P94.9 | DESCENDANTS NOT EXHAUSTIVELY MAPPED | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPCATEGORYID~447637006 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPCATEGORYID~447639009 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPGROUP~1 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPPRIORITY~1 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPPRIORITY~2 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPRULE~IFA 445518008 | Age at onset of clinical finding (observable entity) | < 29.0 days SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPRULE~OTHERWISE TRUE SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPRULE~TRUE SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPTARGET~M62.9 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPTARGET~P94.9 SNOMEDCT_US
SUBSET_MEMBER 900000000000497000~MAPTARGET~X708D SNOMEDCT_US
SUBSET_MEMBER 900000000000497000~MAPTARGET~XUPpE SNOMEDCT_US
SUBSET_MEMBER 900000000000508004~ACCEPTABILITYID~900000000000548007 SNOMEDCT_US
SUBSET_MEMBER 900000000000508004~ACCEPTABILITYID~900000000000549004 SNOMEDCT_US
SUBSET_MEMBER 900000000000509007~ACCEPTABILITYID~900000000000548007 SNOMEDCT_US
SUBSET_MEMBER 900000000000509007~ACCEPTABILITYID~900000000000549004 SNOMEDCT_US
TERMUI T027304 MSH
TERMUI T369134 MSH
TERMUI T369135 MSH
TERMUI T369136 MSH
TH NLM (1966) MSH
TH NLM (2000) MSH
TYPE_ID 900000000000003001 SNOMEDCT_US
TYPE_ID 900000000000013009 SNOMEDCT_US

Additional Concept Data:  (none)

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