amyoplasia congenita disruptive sequence

Preferred Label : amyoplasia congenita disruptive sequence;

Details

Origin ID

D4-00601;

UMLS CUI

C0812412;

Automatic exact mappings (from CISMeF team)
- arthrogryposis [MeSH Descriptor]
- arthrogryposis [MeSH concept]
Currated CISMeF NLP mapping
- Amyoplasia congenita disruptive sequence (disorder) [SNOMED CT concept]
- Arthrogryposis multiplex congenita [ICD-10 Sub-category]
- Arthrogryposis multiplex congenita [HPO term]
- Arthrogryposis multiplex congenita [ICD-11 Sub-sub category]
- Arthrogryposis multiplex congenita [ICD-10 Sub-category (who)]
- Arthrogryposis multiplex congenita [ORDO Disease]
- Arthrogryposis multiplex congenita [OMIM Phenotype]
- Congenital amyoplasia (disorder) [SNOMED CT concept]
- Congenital multiplex arthrogryposis [MedDRA Preferred Term]
- arthrogryposis multiplex congenita [Disease (Nov.)]
ICD-10 exact mapping(s)
- Arthrogryposis multiplex congenita [ICD-10 Sub-category (who)]
Manual BTNT mappings - CISMeF
- Autosomal recessive multiple pterygium syndrome [ORDO Disease]
- Crisponi syndrome [ORDO Disease]
- Fetal akinesia deformation sequence [ORDO Disease]
- Infantile-onset X-linked spinal muscular atrophy [ORDO Disease]
- Marden-Walker syndrome [ORDO Disease]
- Neurogenic arthrogryposis multiplex congenita [ORDO Disease]
- Van den Ende-Gupta syndrome [ORDO Disease]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
Référence SNOMED
- congenital contracture, nos [SNOMED Notion]
- extremity, nos [SNOMED Notion]
- joint, nos [SNOMED Notion]
SNOMED CT concept
- Amyoplasia congenita disruptive sequence (disorder) [SNOMED CT concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Amyoplasia congenita disruptive sequence (disorder) [SNOMED CT concept]
- Congenital amyoplasia (disorder) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

Main resources

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