Patella, familial recurrent dislocation of

Preferred Label : Patella, familial recurrent dislocation of;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal dominant;

Prefixed ID : %169000;

Details

Origin ID

169000;

UMLS CUI

C1868575;

Currated CISMeF NLP mapping
- patella, familial recurrent dislocation of [MeSH concept]
- patella, familial recurrent dislocation of [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Recurrent patellar dislocation [HPO term]
Not associated HPO term(s)
- Joint laxity [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- patella, familial recurrent dislocation of [MeSH Supplementary Concept]
- patella, familial recurrent dislocation of [MeSH concept]

Keyword's position in hierarchy(ies) :

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