Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

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 enzyme/coenzyme activity (HP:0012379)

Parent Node:
Abnormal superoxide dismutase level (HP:0031835)

..Starting node
..Increased superoxide dismutase level (HP:0031836)

Term ID:

31836

Name:

Increased superoxide dismutase level

Synonym:

Increased superoxide:superoxide oxidoreductase activity

Definition:

Increased level of catalysis of the reaction: 2 superoxide + 2 H+ = O2 + hydrogen peroxide.

Comments:

Reference:

HP:0031836

Genes and Diseases:

Child Nodes:

Sister Nodes:

Decreased superoxide dismutase level (HP:0031837)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031836	HP:0031836	Increased superoxide dismutase level	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.