Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Abnormal biliary tract morphology (HP:0012440)

Parent Node:
Abnormal intrahepatic bile duct morphology (HP:0011040)

..Starting node
..Interlobular bile duct destruction (HP:0025344)

Term ID:

25344

Name:

Interlobular bile duct destruction

Synonym:

Definition:

Damage to and obliteration of intrahepatic bile ducts (bile ducts that transport bile between the Canals of Hering and the interlobar bile ducts).

Comments:

Reference:

HP:0025344

Genes and Diseases:

Child Nodes:

Sister Nodes:

Intrahepatic bile duct cysts (HP:0005209)

Intrahepatic biliary atresia (HP:0005248)

Intrahepatic biliary dysgenesis (HP:0001401)

Reduced number of intrahepatic bile ducts (HP:0006571)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025344	HP:0025344	Interlobular bile duct destruction	0	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.