Splenoportal vascular anomalies

Preferred Label : Splenoportal vascular anomalies;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : ? Autosomal recessive; ? secondary to hepatic fibrosis or same as polycystic kidney, type I;

Prefixed ID : 271500;

Détails

Origin ID

271500;

UMLS CUI

C0340826;

Currated CISMeF NLP mapping
- Splenoportal vascular anomaly (disorder) [SNOMED CT concept]
- splenoportal vascular anomalies [MeSH concept]
- splenoportal vascular anomalies [MeSH Supplementary Concept]
HPO term(s)
- Anomalous splenoportal venous system [HPO term]
- Ascites [HPO term]
- Autosomal recessive inheritance [HPO term]
- Chronic hepatic encephalopathy [HPO term]
- Cirrhosis [HPO term]
- Diabetes mellitus [HPO term]
- Hepatic fibrosis [HPO term]
- Hyperammonemia [HPO term]
- Mild diabetes mellitus [HPO term]
- Splenomegaly [HPO term]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Splenoportal vascular anomaly (disorder) [SNOMED CT concept]
- splenoportal vascular anomalies [MeSH Supplementary Concept]
- splenoportal vascular anomalies [MeSH concept]

Position du mot-clé dans l'(les) arborescence(s) :

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