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 visual electrophysiology (HP:0030453)

Parent Node:
Abnormal electrooculogram (HP:0030454)

..Starting node
..Increased Arden ratio of electrooculogram (HP:0031155)

Term ID:

31155

Name:

Increased Arden ratio of electrooculogram

Synonym:

Increased Arden ratio of EOG

Definition:

An abnormal increase in the Arden ratio, which is the ratio between the light peak and the dark trough of the smoothed (physiologic) EOG record.

Comments:

Reference:

HP:0031155

Genes and Diseases:

Child Nodes:

Sister Nodes:

Decreased Arden ratio of electrooculogram (HP:0008179)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031155	HP:0031155	Increased Arden ratio of electrooculogram	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.