arthrogryposis - CISMeF

CISMeF

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ArthrogryposisSNOMED Notion

Preferred Label : arthrogryposis;

Details

Origin ID

D1-502A0;

UMLS CUI

C0003886;

Automatic exact mappings (from CISMeF team)
- Anion gap [LOINC component]
- Anion gap [MedDRA Preferred Term]
- Atrophic gastritis (disorder) [SNOMED CT concept]
- Chronic atrophic gastritis of unknown aetiology [ICD-11 Sub-sub category]
- Left atrium [FMA entity]
- acid-base equilibrium [MeSH Descriptor]
- agonists [MeSH Qualifier]
- anesthesia, general [MeSH Descriptor]
- anion gap [MeSH concept]
- antigens [MeSH Descriptor]
- fatty acids [MeSH Descriptor]
Currated CISMeF NLP mapping
- Arthrogryposis [PASCAL descriptor]
- Arthrogryposis [NCIt concept]
- Arthrogryposis [HRDO Sign]
- Arthrogryposis (disorder) [SNOMED CT concept]
- Arthrogryposis syndrome [ORDO Disease]
- arthrogryposis [Disease (Nov.)]
- arthrogryposis [MeSH Descriptor]
- arthrogryposis [MeSH concept]
False automatic mappings
- Arthrogryposis multiplex congenita [HPO term]
ICD-10 exact mapping(s)
- Other specified disorders of muscle | site unspecified [ICD-10 Subdivision (who)]
Manual BTNT mappings - CISMeF
- Adducted thumbs-arthrogryposis syndrome, Christian type [ORDO Disease]
- Arthrogryposis due to muscular dystrophy [ORDO Disease]
- Arthrogryposis-anterior horn cell disease syndrome [ORDO Disease]
- Arthrogryposis-hyperkeratosis syndrome, lethal form [ORDO Disease]
- Arthrogryposis-renal dysfunction-cholestasis syndrome [ORDO Disease]
- CAMFAK syndrome [ORDO Disease]
- Distal arthrogryposis [ORDO Disease]
- Hypomyelination neuropathy-arthrogryposis syndrome [ORDO Disease]
- Kuskokwim syndrome [ORDO Disease]
- Lethal multiple pterygium syndrome [ORDO Disease]
- Multiple pterygium syndrome, Aslan type [ORDO Disease]
- Multiple pterygium-malignant hyperthermia syndrome [ORDO Disease]
- Musculocontractural Ehlers-Danlos syndrome [ORDO Disease]
- Pelvic dysplasia-arthrogryposis of lower limbs syndrome [ORDO Disease]
- X-linked lethal multiple pterygium syndrome [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Sucking/swallowing disorder associated with a neuromuscular disease [ORDO Disease]
- Syndrome or malformation associated with head and neck malformations [ORDO Disease]
- Syndrome with limb malformations as a major feature [ORDO Disease]
Metaterm(s)
- rheumatology [CISMeF Metaterm]
Référence SNOMED
- contracture, nos [SNOMED Notion]
- extremity, nos [SNOMED Notion]
- joint, nos [SNOMED Notion]
SNOMED CT concept
- Arthrogryposis (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Arthrogryposis [HRDO Sign]
- Arthrogryposis [PASCAL descriptor]
- Arthrogryposis [NCIt concept]
- Arthrogryposis (disorder) [SNOMED CT concept]
- Arthrogryposis multiplex congenita [OMIM Phenotype]
- Arthrogryposis multiplex congenita [ICD-10 Sub-category]
- Arthrogryposis multiplex congenita [HPO term]
- Arthrogryposis multiplex congenita [ICD-10 Sub-category (who)]
- Arthrogryposis syndrome [ORDO Disease]
- Congenital multiplex arthrogryposis [MedDRA Preferred Term]
- arthrogryposis [MeSH Descriptor]
- arthrogryposis [MeSH concept]
- arthrogryposis [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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26/04/2024

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