Hyperheparinemia

Preferred Label : Hyperheparinemia;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 144050;

Details

Origin ID

144050;

UMLS CUI

C3203346;

Automatic exact mappings (from CISMeF team)
- Haemorrhagic disorder due to circulating anticoagulants [ICD-10 Sub-category (who)]
Currated CISMeF NLP mapping
- Hyperheparinemia (disorder) [SNOMED CT concept]
- hyperheparinemia [SNOMED Notion]
- hyperheparinemia [MeSH concept]
- hyperheparinemia [MeSH Supplementary Concept]
HPO term(s)
- Abnormal bleeding [HPO term]
- Autosomal dominant inheritance [HPO term]
- Congenital bleeding diathesis [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hyperheparinemia (disorder) [SNOMED CT concept]
- hyperheparinemia [MeSH Supplementary Concept]
- hyperheparinemia [SNOMED Notion]
- hyperheparinemia [MeSH concept]

Keyword's position in hierarchy(ies) :

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