Priapism, familial idiopathic

Preferred Label : Priapism, familial idiopathic;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant form;

Prefixed ID : 176620;

Details

Origin ID

176620;

UMLS CUI

C1867771;

Currated CISMeF NLP mapping
- Priapism, familial idiopathic [MeSH concept]
- priapism, familial idiopathic [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Priapism [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Priapism, familial idiopathic [MeSH concept]
- priapism, familial idiopathic [MeSH Supplementary Concept]

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