Joint laxity, familial

Preferred Label : Joint laxity, familial;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Eds XI; Eds11; Ehlers-danlos syndrome, type XI; Articular hypermobility syndrome; Familial joint instability syndrome;

Inheritance : Autosomal dominant;

Prefixed ID : %147900;

Details

Origin ID

147900;

UMLS CUI

C0268349;

Currated CISMeF NLP mapping
- Ehlers-Danlos syndrome, familial joint laxity type (disorder) [SNOMED CT concept]
- Ehlers-Danlos syndrome, type 11 [ICD-11 More detail]
- Familial articular hypermobility syndrome [ORDO Disease]
- Familial joint laxity [ICD-11 More detail]
- Joint laxity, familial [MeSH concept]
- ehlers-danlos syndrome, familial joint laxity type [SNOMED Notion]
- joint laxity, familial [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Congenital hip dislocation [HPO term]
- Joint laxity [HPO term]
- Recurrent joint dislocation [HPO term]
ORDO concept(s)
- Familial articular hypermobility syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Ehlers-Danlos syndrome, familial joint laxity type (disorder) [SNOMED CT concept]
- Familial articular hypermobility syndrome [ORDO Disease]
- Familial joint laxity [ICD-11 More detail]
- Joint laxity, familial [MeSH concept]
- ehlers-danlos syndrome, familial joint laxity type [SNOMED Notion]
- joint laxity, familial [MeSH Supplementary Concept]

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