muscular diseases - CISMeF

CISMeF

chu

Muscular diseasesMeSH Descriptor

Preferred Label : muscular diseases;

MeSH definition : Acquired, familial, and congenital disorders of SKELETAL MUSCLE and SMOOTH MUSCLE.;

MeSH synonym : myopathies; muscular disease; myopathy; muscle disorders; muscle disorder; myopathic conditions; myopathic condition;

MeSH annotation : GEN; prefer specifics; inflamm dis MYOSITIS. /congen: consider also Myopathies, Structural, Congenital & its indentions; general or unspecified; prefer specifics; inflammatory disease equals MYOSITIS; /congen: consider also Myopathies, Structural, Congenital & its indentions;

Wikipedia link : https://en.wikipedia.org/wiki/Muscular diseases;

Details

Origin ID

D009135;

UMLS CUI

C0026848;

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]
Currated CISMeF NLP mapping
- Certain specified disorders of muscle [ICD-11 Category]
- Disorder muscle [MedDRA LLT]
- Disorder of skeletal AND/OR smooth muscle (disorder) [SNOMED CT concept]
- Disorder of skeletal muscle (disorder) [SNOMED CT concept]
- MUSCLE DISORDER [WHO-ART Included Term]
- MYOPATHY [WHO-ART High Level Term]
- Muscle disorder [MedDRA Preferred Term]
- Muscle disorder NOS [MedDRA LLT]
- Muscle disorders [MedDRA High Level Group Term]
- Myopathies [MedDRA High Level Term]
- Myopathy [NCIt concept]
- Myopathy [PASCAL descriptor]
- Myopathy [ICD-11 More detail]
- Myopathy [MedDRA Preferred Term]
- Myopathy [HPO term]
- Myopathy [HRDO Sign]
- Myopathy, unspecified [ICD-10 Sub-category (who)]
- Myopathy, unspecified [ICD-10 Sub-category]
- Myopathy, unspecified [ICD-9 code]
- Other myopathies [ICD-9 code]
- Skeletal muscle disease [ORDO Disease]
- disorder of muscle, nos [SNOMED Notion]
- muscle disorder [Disease (Nov.)]
- muscle disorders [MedlinePlus Topic]
- muscular disease [DO Concept]
- myopathy [DO Concept]
- myopathy, nos [SNOMED Notion]
DO Cross reference
- myopathy [DO Concept]
HPO term
- Myopathy [HPO term]
MedlinePlus topic(s)
- muscle disorders [MedlinePlus Topic]
ORDO relation(s)
- Skeletal muscle disease [ORDO Disease]
Record concept(s)
- muscular diseases [MeSH concept]
Related MeSH Supplementary Concept(s)
- Alpha-B crystallinopathy [MeSH Supplementary Concept]
- Chanarin-Dorfman Syndrome [MeSH Supplementary Concept]
- Kocher-Debre-Semelaigne syndrome [MeSH Supplementary Concept]
- Marinesco-Sjogren-like syndrome (MSLS) [MeSH Supplementary Concept]
- VLCAD deficiency [MeSH Supplementary Concept]
- anal sphincter myopathy, internal [MeSH Supplementary Concept]
- aplasia of extensor muscles of fingers, unilateral, with generalized polyneuropathy [MeSH Supplementary Concept]
- camptodactyly, fibrous tissue hyperplasia, and skeletal dysplasia [MeSH Supplementary Concept]
- carnitine palmitoyltransferase II deficiency, Late-Onset [MeSH Supplementary Concept]
- dimauro disease [MeSH Supplementary Concept]
- encephalopathy, axonal, with necrotizing myopathy, cardiomyopathy, and cataracts [MeSH Supplementary Concept]
- epiphyseal dysplasia, multiple, with myopathy [MeSH Supplementary Concept]
- erythrocyte amp deaminase deficiency [MeSH Supplementary Concept]
- erythrocyte lactate transporter defect [MeSH Supplementary Concept]
- fingerprint body myopathy [MeSH Supplementary Concept]
- hereditary myopathy with early respiratory failure [MeSH Supplementary Concept]
- hypertrophia musculorum vera [MeSH Supplementary Concept]
- mitochondrial DNA depletion syndrome, myopathic form [MeSH Supplementary Concept]
- muscular hypoplasia, congenital universal, of krabbe [MeSH Supplementary Concept]
- myopathic carnitine deficiency [MeSH Supplementary Concept]
- myopathy due to Malate-Aspartate shuttle defect [MeSH Supplementary Concept]
- myopathy with giant abnormal mitochondria [MeSH Supplementary Concept]
- myopathy with lactic acidosis, hereditary [MeSH Supplementary Concept]
- myopathy, Early-Onset, with fatal cardiomyopathy [MeSH Supplementary Concept]
- myopathy, X-Linked, with excessive autophagy [MeSH Supplementary Concept]
- myopathy, cataract, hypogonadism syndrome [MeSH Supplementary Concept]
- myopathy, congenital nonprogressive with moebius and robin sequences [MeSH Supplementary Concept]
- myopathy, congenital, with excess of muscle spindles [MeSH Supplementary Concept]
- myopathy, granulovacuolar lobular, with electrical myotonia [MeSH Supplementary Concept]
- myopathy, hyaline body, autosomal recessive [MeSH Supplementary Concept]
- myopathy, myosin storage [MeSH Supplementary Concept]
- myopathy, reducing body, X-Linked, Childhood-Onset [MeSH Supplementary Concept]
- myopathy, reducing body, X-Linked, Early-Onset, severe [MeSH Supplementary Concept]
- myostatin-related muscle hypertrophy [MeSH Supplementary Concept]
- neutral lipid storage disease with myopathy [MeSH Supplementary Concept]
- ophthalmoplegic neuromuscular disorder with abnormal mitochondria [MeSH Supplementary Concept]
- optic atrophy, deafness, ophthalmoplegia, and myopathy [MeSH Supplementary Concept]
- pectoralis muscle, absence of [MeSH Supplementary Concept]
- proximal myopathy with focal depletion of mitochondria [MeSH Supplementary Concept]
- rippling muscle disease, 1 [MeSH Supplementary Concept]
- secretory diarrhea, myopathy, and deafness [MeSH Supplementary Concept]
- singleton merten syndrome [MeSH Supplementary Concept]
- systemic carnitine deficiency [MeSH Supplementary Concept]
- tel hashomer camptodactyly syndrome [MeSH Supplementary Concept]
- treft sanborn carey syndrome [MeSH Supplementary Concept]
- uruguay faciocardiomusculoskeletal syndrome [MeSH Supplementary Concept]
- vacuolar myopathy [MeSH Supplementary Concept]
See also (suggested by CISMeF)
- muscle fatigue [MeSH Descriptor]
- neoplasms, muscle tissue [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Disorder muscle [MedDRA LLT]
- Disorder of muscle, unspecified [ICD-10 Sub-category]
- Disorder of muscle, unspecified [ICD-10 Sub-category (who)]
- Disorder of skeletal AND/OR smooth muscle (disorder) [SNOMED CT concept]
- MUSCLE DISORDER [WHO-ART Included Term]
- MYOPATHY [WHO-ART High Level Term]
- Muscle disorder [MedDRA Preferred Term]
- Muscle disorder NOS [MedDRA LLT]
- Muscle disorders [MedDRA High Level Group Term]
- Myopathies [MedDRA High Level Term]
- Myopathy [MedDRA Preferred Term]
- Myopathy [NCIt concept]
- Myopathy [HPO term]
- Myopathy [HRDO Sign]
- Myopathy [PASCAL descriptor]
- Myopathy, unspecified [MedDRA LLT]
- Myopathy, unspecified [ICD-9 code]
- Myopathy, unspecified [ICD-10 Sub-category]
- Myopathy, unspecified [ICD-10 Sub-category (who)]
- disorder of muscle, nos [SNOMED Notion]
- muscle disorder [Disease (Nov.)]
- muscle disorders [MedlinePlus Topic]
- muscular disease [DO Concept]
- myopathy [DO Concept]
- myopathy, nos [SNOMED Notion]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients

Nous contacter.
20/05/2024

© Rouen University Hospital. Any partial or total use of this material must mention the source.

muscular diseases - CISMeF

CISMeF

chu

Muscular diseasesMeSH Descriptor

Preferred Label : muscular diseases;

MeSH definition : Acquired, familial, and congenital disorders of SKELETAL MUSCLE and SMOOTH MUSCLE.;

MeSH synonym : myopathies; muscular disease; myopathy; muscle disorders; muscle disorder; myopathic conditions; myopathic condition;

MeSH annotation : GEN; prefer specifics; inflamm dis MYOSITIS. /congen: consider also Myopathies, Structural, Congenital & its indentions; general or unspecified; prefer specifics; inflammatory disease equals MYOSITIS; /congen: consider also Myopathies, Structural, Congenital & its indentions;

Wikipedia link : https://en.wikipedia.org/wiki/Muscular diseases;

Details

Origin ID

D009135;

UMLS CUI

C0026848;

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]
Currated CISMeF NLP mapping
- Certain specified disorders of muscle [ICD-11 Category]
- Disorder muscle [MedDRA LLT]
- Disorder of skeletal AND/OR smooth muscle (disorder) [SNOMED CT concept]
- Disorder of skeletal muscle (disorder) [SNOMED CT concept]
- MUSCLE DISORDER [WHO-ART Included Term]
- MYOPATHY [WHO-ART High Level Term]
- Muscle disorder [MedDRA Preferred Term]
- Muscle disorder NOS [MedDRA LLT]
- Muscle disorders [MedDRA High Level Group Term]
- Myopathies [MedDRA High Level Term]
- Myopathy [NCIt concept]
- Myopathy [PASCAL descriptor]
- Myopathy [ICD-11 More detail]
- Myopathy [MedDRA Preferred Term]
- Myopathy [HPO term]
- Myopathy [HRDO Sign]
- Myopathy, unspecified [ICD-10 Sub-category (who)]
- Myopathy, unspecified [ICD-10 Sub-category]
- Myopathy, unspecified [ICD-9 code]
- Other myopathies [ICD-9 code]
- Skeletal muscle disease [ORDO Disease]
- disorder of muscle, nos [SNOMED Notion]
- muscle disorder [Disease (Nov.)]
- muscle disorders [MedlinePlus Topic]
- muscular disease [DO Concept]
- myopathy [DO Concept]
- myopathy, nos [SNOMED Notion]
DO Cross reference
- myopathy [DO Concept]
HPO term
- Myopathy [HPO term]
MedlinePlus topic(s)
- muscle disorders [MedlinePlus Topic]
ORDO relation(s)
- Skeletal muscle disease [ORDO Disease]
Record concept(s)
- muscular diseases [MeSH concept]
Related MeSH Supplementary Concept(s)
- Alpha-B crystallinopathy [MeSH Supplementary Concept]
- Chanarin-Dorfman Syndrome [MeSH Supplementary Concept]
- Kocher-Debre-Semelaigne syndrome [MeSH Supplementary Concept]
- Marinesco-Sjogren-like syndrome (MSLS) [MeSH Supplementary Concept]
- VLCAD deficiency [MeSH Supplementary Concept]
- anal sphincter myopathy, internal [MeSH Supplementary Concept]
- aplasia of extensor muscles of fingers, unilateral, with generalized polyneuropathy [MeSH Supplementary Concept]
- camptodactyly, fibrous tissue hyperplasia, and skeletal dysplasia [MeSH Supplementary Concept]
- carnitine palmitoyltransferase II deficiency, Late-Onset [MeSH Supplementary Concept]
- dimauro disease [MeSH Supplementary Concept]
- encephalopathy, axonal, with necrotizing myopathy, cardiomyopathy, and cataracts [MeSH Supplementary Concept]
- epiphyseal dysplasia, multiple, with myopathy [MeSH Supplementary Concept]
- erythrocyte amp deaminase deficiency [MeSH Supplementary Concept]
- erythrocyte lactate transporter defect [MeSH Supplementary Concept]
- fingerprint body myopathy [MeSH Supplementary Concept]
- hereditary myopathy with early respiratory failure [MeSH Supplementary Concept]
- hypertrophia musculorum vera [MeSH Supplementary Concept]
- mitochondrial DNA depletion syndrome, myopathic form [MeSH Supplementary Concept]
- muscular hypoplasia, congenital universal, of krabbe [MeSH Supplementary Concept]
- myopathic carnitine deficiency [MeSH Supplementary Concept]
- myopathy due to Malate-Aspartate shuttle defect [MeSH Supplementary Concept]
- myopathy with giant abnormal mitochondria [MeSH Supplementary Concept]
- myopathy with lactic acidosis, hereditary [MeSH Supplementary Concept]
- myopathy, Early-Onset, with fatal cardiomyopathy [MeSH Supplementary Concept]
- myopathy, X-Linked, with excessive autophagy [MeSH Supplementary Concept]
- myopathy, cataract, hypogonadism syndrome [MeSH Supplementary Concept]
- myopathy, congenital nonprogressive with moebius and robin sequences [MeSH Supplementary Concept]
- myopathy, congenital, with excess of muscle spindles [MeSH Supplementary Concept]
- myopathy, granulovacuolar lobular, with electrical myotonia [MeSH Supplementary Concept]
- myopathy, hyaline body, autosomal recessive [MeSH Supplementary Concept]
- myopathy, myosin storage [MeSH Supplementary Concept]
- myopathy, reducing body, X-Linked, Childhood-Onset [MeSH Supplementary Concept]
- myopathy, reducing body, X-Linked, Early-Onset, severe [MeSH Supplementary Concept]
- myostatin-related muscle hypertrophy [MeSH Supplementary Concept]
- neutral lipid storage disease with myopathy [MeSH Supplementary Concept]
- ophthalmoplegic neuromuscular disorder with abnormal mitochondria [MeSH Supplementary Concept]
- optic atrophy, deafness, ophthalmoplegia, and myopathy [MeSH Supplementary Concept]
- pectoralis muscle, absence of [MeSH Supplementary Concept]
- proximal myopathy with focal depletion of mitochondria [MeSH Supplementary Concept]
- rippling muscle disease, 1 [MeSH Supplementary Concept]
- secretory diarrhea, myopathy, and deafness [MeSH Supplementary Concept]
- singleton merten syndrome [MeSH Supplementary Concept]
- systemic carnitine deficiency [MeSH Supplementary Concept]
- tel hashomer camptodactyly syndrome [MeSH Supplementary Concept]
- treft sanborn carey syndrome [MeSH Supplementary Concept]
- uruguay faciocardiomusculoskeletal syndrome [MeSH Supplementary Concept]
- vacuolar myopathy [MeSH Supplementary Concept]
See also (suggested by CISMeF)
- muscle fatigue [MeSH Descriptor]
- neoplasms, muscle tissue [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Disorder muscle [MedDRA LLT]
- Disorder of muscle, unspecified [ICD-10 Sub-category]
- Disorder of muscle, unspecified [ICD-10 Sub-category (who)]
- Disorder of skeletal AND/OR smooth muscle (disorder) [SNOMED CT concept]
- MUSCLE DISORDER [WHO-ART Included Term]
- MYOPATHY [WHO-ART High Level Term]
- Muscle disorder [MedDRA Preferred Term]
- Muscle disorder NOS [MedDRA LLT]
- Muscle disorders [MedDRA High Level Group Term]
- Myopathies [MedDRA High Level Term]
- Myopathy [MedDRA Preferred Term]
- Myopathy [NCIt concept]
- Myopathy [HPO term]
- Myopathy [HRDO Sign]
- Myopathy [PASCAL descriptor]
- Myopathy, unspecified [MedDRA LLT]
- Myopathy, unspecified [ICD-9 code]
- Myopathy, unspecified [ICD-10 Sub-category]
- Myopathy, unspecified [ICD-10 Sub-category (who)]
- disorder of muscle, nos [SNOMED Notion]
- muscle disorder [Disease (Nov.)]
- muscle disorders [MedlinePlus Topic]
- muscular disease [DO Concept]
- myopathy [DO Concept]
- myopathy, nos [SNOMED Notion]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients

Nous contacter.
20/05/2024

© Rouen University Hospital. Any partial or total use of this material must mention the source.