Human Phenotype Ontology

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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 macrophage morphology (HP:0004311)

Parent Node:
Abnormal liver morphology (HP:0410042)

Parent Node:
Granulomatosis (HP:0002955)

..Starting node
..Hepatic granulomatosis (HP:0011955)

Term ID:

11955

Name:

Hepatic granulomatosis

Synonym:

Definition:

The presence of multiple granulomas in the liver as based on pathological examination. Granulomas are small 0.5 to 2 mm collections of modified macrophages called epithelioid cells usually surrounded by lymphocytes.

Comments:

Reference:

HP:0011955

Genes and Diseases:

Child Nodes:

Sister Nodes:

Cerebral granulomatosis (HP:0100313)

Lipogranulomatosis (HP:0040139)

Non-caseating epithelioid cell granulomatosis (HP:0012220)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011955	HP:0011955	Hepatic granulomatosis	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.

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