Human Phenotype Ontology 
Grandparent Node:
expandAbnormal liver morphology (HP:0410042)help
Grandparent Node:
expandAbnormality of the vasculature (HP:0002597)help
Parent Node:
expandAbnormality of the hepatic vasculature (HP:0006707)help
..Starting node
..expandIntrahepatic portal vein sclerosis (HP:0031015)help
Term ID: 31015
Name: Intrahepatic portal vein sclerosis
Synonym: Idiopathic non-cirrhotic portal hypertension; Incomplete septal cirrhosis; Non cirrhotic portal fibrosis; Obliterative portal venopathy
Definition: Sclerosis of the intrahepatic portal veins of the liver and generally accompanied by non-cirrhotic portal hypertension, features of which may include splenomegaly and varices.
Comments:
Reference: HP:0031015
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAnomalous splenoportal venous system (HP:0005201) help
..expandHepatic arteriovenous malformation (HP:0006574) help
..expandHepatic vascular malformations (HP:0006576) help
..expandPortal hypertension (HP:0001409) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031015HP:0031015Intrahepatic portal vein sclerosis0 CL E G H


Genes (0) :

Diseases (0) :
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.