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 morphology of myocardial trabeculae (HP:0030681)

Parent Node:
Abnormal morphology of left ventricular trabeculae (HP:0031192)

..Starting node
..Thin myocardium compact layer (HP:0031196)

Term ID:

31196

Name:

Thin myocardium compact layer

Synonym:

Definition:

Reduced thickness of the outer, dense layer of the myocardium.

Comments:

Reference:

HP:0031196

Genes and Diseases:

Child Nodes:

Sister Nodes:

Apical hypertrabeculation of the left ventricle (HP:0031195)

Increased density of left ventricular trabeculae (HP:0031194)

Left ventricular noncompaction (HP:0030682)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031196	HP:0031196	Thin myocardium compact layer	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.