Arthrogryposis

Preferred Label : Arthrogryposis;

NCIt related terms : Congenital articular rigidity with myopathy;

NCIt definition : A rare, non-progressive congenital disorder characterized by multiple joint contractures which are present at birth.;

Details

Origin ID

C84572;

UMLS CUI

C0003886;

Automatic exact mappings (from CISMeF team)
- Arthrogryposis multiplex congenita [HPO term]
- Other specified disorders of muscle [ICD-10 Sub-category (who)]
Currated CISMeF NLP mapping
- Arthrogryposis [HRDO Sign]
- Arthrogryposis [PASCAL descriptor]
- Arthrogryposis (disorder) [SNOMED CT concept]
- Arthrogryposis syndrome [ORDO Disease]
- arthrogryposis [Disease (Nov.)]
- arthrogryposis [MeSH Descriptor]
- arthrogryposis [MeSH concept]
- arthrogryposis [SNOMED Notion]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Arthrogryposis [HRDO Sign]
- Arthrogryposis [PASCAL descriptor]
- 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 [Disease (Nov.)]
- arthrogryposis [MeSH concept]
- arthrogryposis [MeSH Descriptor]
- arthrogryposis [SNOMED Notion]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- NICHD Terminology [NCIt concept]
- Neonatal Research Network Terminology [NCIt concept]
disease_has_finding
- Rare Lesion [NCIt concept]

Keyword's position in hierarchy(ies) :

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