Pseudoarthrogryposis

Preferred Label : Pseudoarthrogryposis;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Ankylosis at elbow and knee; Hereditary congenital rigidity of elbows and knees;

Inheritance : Autosomal dominant;

Prefixed ID : 177300;

Details

Origin ID

177300;

UMLS CUI

C1867485;

Currated CISMeF NLP mapping
- pseudoarthrogryposis [MeSH concept]
- pseudoarthrogryposis [MeSH Supplementary Concept]
HPO term(s)
- Ankylosis [HPO term]
- Autosomal dominant inheritance [HPO term]
- Limited elbow movement [HPO term]
- Proximal tibial and fibular fusion [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- pseudoarthrogryposis [MeSH Supplementary Concept]
- pseudoarthrogryposis [MeSH concept]

Keyword's position in hierarchy(ies) :

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