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 heart morphology (HP:0001627)

Parent Node:
Abnormal myocardium morphology (HP:0001637)

..Starting node
..Myocardial immune cell infiltration (HP:0031321)

Term ID:

31321

Name:

Myocardial immune cell infiltration

Synonym:

Definition:

An increase in the number of immune cells in myocardial tissue (which can be assumed to have migrated into the myocardium).

Comments:

Reference:

HP:0031321

Genes and Diseases:

Child Nodes:

........

Myocardial lymphocytic infiltration (HP:0031322)

........

Myocardial eosinophilic infiltration (HP:0031323)

........

Myocardial multinucleated giant cells (HP:0031324)

........

Myocardial granulomatous infiltrates (HP:0031325)

........

Perivascular myocardial immune cell infiltration (HP:0031330)

Sister Nodes:

Abnormal morphology of myocardial trabeculae (HP:0030681)

Abnormal ventricular myocardium morphology (HP:0031316)

Cardiac amyloidosis (HP:0030843)

Cardiomyopathy (HP:0001638)

Fatty replacement of ventricular myocardial tissue (HP:0031317)

Focal necrosis of right ventricular muscle cells (HP:0003338)

Myocardial fibrosis (HP:0001685)

Myocardial necrosis (HP:0001700)

Myocarditis (HP:0012819)

Myofiber disarray (HP:0031318)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031321	HP:0031321	Myocardial immune cell infiltration	0	CL E G H
HP:0031321	HP:0031330	Perivascular myocardial immune cell infiltration	1	CL E G H
HP:0031321	HP:0031325	Myocardial granulomatous infiltrates	1	CL E G H
HP:0031321	HP:0031324	Myocardial multinucleated giant cells	1	CL E G H
HP:0031321	HP:0031323	Myocardial eosinophilic infiltration	1	CL E G H
HP:0031321	HP:0031322	Myocardial lymphocytic infiltration	1	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.