Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the cardiovascular system (HP:0001626)help
Parent Node:
expandAbnormal liver morphology (HP:0410042)help
Parent Node:
expandAbnormality of the vasculature (HP:0002597)help
..Starting node
..expandAbnormality of the hepatic vasculature (HP:0006707)help
Term ID: 6707
Name: Abnormality of the hepatic vasculature
Synonym: Abnormality of liver blood vessels; Abnormality of the liver vasculature
Definition: An abnormality of the hepatic vasculature.
Comments:
Reference: HP:0006707
Genes and Diseases:
 
       Child Nodes:
........expandPortal hypertension (HP:0001409) help
................... HP:0004941 Extrahepatic portal hypertension
........expandAnomalous splenoportal venous system (HP:0005201) help
........expandHepatic arteriovenous malformation (HP:0006574) help
........expandHepatic vascular malformations (HP:0006576) help
........expandIntrahepatic portal vein sclerosis (HP:0031015) help

 Sister Nodes: 
..expandAbnormal cerebral vascular morphology (HP:0100659) help
..expandAbnormal vascular morphology (HP:0025015) help
..expandAbnormal vascular physiology (HP:0030163) help
..expandAbnormality of gastrointestinal vasculature (HP:0004296) help
..expandAbnormality of head blood vessel (HP:3000036) help
..expandAbnormality of infraorbital artery (HP:3000060) help
..expandAbnormality of neck blood vessel (HP:3000037) help
..expandAbnormality of the pulmonary vasculature (HP:0004930) help
..expandAbnormality of the vasculature of the eye (HP:0008047) help
..expandVascular neoplasm (HP:0100742) help
..expandVascular skin abnormality (HP:0011276) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0006707HP:0006707Abnormality of the hepatic vasculature0 CL E G H
HP:0006707HP:0001409Portal hypertension1 CL E G H
HP:0006707HP:0006576Hepatic vascular malformations1 CL E G H
HP:0006707HP:0031941Abnormal portal venous system morphology1 CL E G H
HP:0006707HP:0032181Anomalous hepatic venous drainage into the left atrium1 CL E G H
HP:0006707HP:0006574Hepatic arteriovenous malformation1 CL E G H
HP:0006707HP:0005201Anomalous splenoportal venous system2 CL E G H
HP:0006707HP:0031015Intrahepatic portal vein sclerosis2 CL E G H
HP:0006707HP:0004941Extrahepatic portal hypertension2 CL E G H
HP:0006707HP:0031942Congenital absence of portal vein2 CL E G H


Genes (51) :ACVRL1 ADA2 ALMS1 ARHGAP31 BTNL2 CC2D2A CLDN1 DCDC2 DGUOK DLL4 DOCK6 ELN ENG EOGT F5 GBE1 GDF2 GLIS3 GPR35 HLA-DRB1 IL12A IL12RB1 INPP5E IRF5 JAK2 KRIT1 MLXIPL MMEL1 MPL MST1 NEUROG3 NOTCH1 NPHP3 PIGM PKHD1 POU2AF1 RBPJ RECQL4 RPGRIP1L SHPK SLC30A10 SMAD4 SP110 SPIB STN1 TCF4 TET2 TJP2 TMEM67 TNFSF15 TNPO3

Diseases (34) :774 600376 615688 64 974 797 216360 1454 59303 617394 251880 617068 616589 194050 187300 131 232500 615506 610199 171 186 729 116860 83620 267010 610293 263200 440713 309854 175050 79124 617341 615878 218600
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.