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:
Clinical modifier (HP:0012823)

Parent Node:
Position (HP:0012830)

..Starting node
..Laterality (HP:0012831)

Term ID:

12831

Name:

Laterality

Synonym:

Definition:

The localization with respect to the side of the body of the specified phenotypic abnormality.

Comments:

Reference:

HP:0012831

Genes and Diseases:

Child Nodes:

........

Bilateral (HP:0012832)

........

Unilateral (HP:0012833)

........

Right (HP:0012834)

........

Left (HP:0012835)

Sister Nodes:

Spatial pattern (HP:0012836)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012831	HP:0012831	Laterality	0	CL E G H
HP:0012831	HP:0012832	Bilateral	1	CL E G H
HP:0012831	HP:0012835	Left	1	CL E G H
HP:0012831	HP:0012834	Right	1	CL E G H
HP:0012831	HP:0012833	Unilateral	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.