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 myocardium morphology (HP:0001637)

Parent Node:
Myocardial immune cell infiltration (HP:0031321)

..Starting node
..Myocardial granulomatous infiltrates (HP:0031325)

Term ID:

31325

Name:

Myocardial granulomatous infiltrates

Synonym:

Definition:

The presence of multiple granulomata (small nodular inflammatory lesions containing grouped mononuclear phagocytes) in the myocardium.

Comments:

Reference:

HP:0031325

Genes and Diseases:

Child Nodes:

Sister Nodes:

Myocardial eosinophilic infiltration (HP:0031323)

Myocardial lymphocytic infiltration (HP:0031322)

Myocardial multinucleated giant cells (HP:0031324)

Perivascular myocardial immune cell infiltration (HP:0031330)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031325	HP:0031325	Myocardial granulomatous infiltrates	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.