Epistaxis, hereditary

Preferred Label : Epistaxis, hereditary;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 132500;

Details

Origin ID

132500;

UMLS CUI

C0339819;

Currated CISMeF NLP mapping
- Hereditary epistaxis (disorder) [Inactive SNOMED CT concept]
- epistaxis, hereditary [MeSH concept]
- epistaxis, hereditary [MeSH Supplementary Concept]
- hereditary epistaxis [Disease (Nov.)]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Epistaxis [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary epistaxis (disorder) [Inactive SNOMED CT concept]
- epistaxis, hereditary [MeSH Supplementary Concept]
- epistaxis, hereditary [MeSH concept]
- hereditary epistaxis [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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