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:
Neoplasm by anatomical site (HP:0011793)

Parent Node:
Abnormal pericardium morphology (HP:0001697)

Parent Node:
Malignant mesothelioma (HP:0100001)

..Starting node
..Pericardial mesothelioma (HP:0100004)

Term ID:

100004

Name:

Pericardial mesothelioma

Synonym:

Definition:

A Malignant mesothelioma originating from cells of the pericardium (the thin layer of mesothelium lining the heart).

Comments:

Reference:

HP:0100004

Genes and Diseases:

Child Nodes:

Sister Nodes:

Peritoneal mesothelioma (HP:0100003)

Pleural mesothelioma (HP:0100002)

Testicular mesothelioma (HP:0100005)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100004	HP:0100004	Pericardial mesothelioma	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.