Portal vein, cavernous transformation of

Preferred Label : Portal vein, cavernous transformation of;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 601004;

Details

Origin ID

601004;

UMLS CUI

C1832917;

Automatic exact mappings (from CISMeF team)
- Primitive portal vein thrombosis [ORDO Disease]
Currated CISMeF NLP mapping
- Portal vein cavernous transformation [MedDRA Preferred Term]
- portal vein, cavernous transformation of [MeSH concept]
- portal vein, cavernous transformation of [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Extrahepatic portal hypertension [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Portal vein cavernous transformation [MedDRA Preferred Term]
- portal vein, cavernous transformation of [MeSH Supplementary Concept]
- portal vein, cavernous transformation of [MeSH concept]

Keyword's position in hierarchy(ies) :

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