Human Phenotype Ontology

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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)

Grandparent Node:
Increased inflammatory response (HP:0012649)

Parent Node:
Cholangitis (HP:0030151)

..Starting node
..Pleomorphic cholangitis (HP:0030990)

Term ID:

30990

Name:

Pleomorphic cholangitis

Synonym:

Definition:

Cholangitis associated with mixed inflammatory infiltrates and the presence of fibrosis or sclerosis of the biliary tree.

Comments:

Reference:

HP:0030990

Genes and Diseases:

Child Nodes:

Sister Nodes:

Granulomatous cholangitis (HP:0030988)

Lymphoid cholangitis (HP:0030989)

Sclerosing cholangitis (HP:0030991)

Suppurative cholangitis (HP:0030987)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030990	HP:0030990	Pleomorphic cholangitis	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.