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:
Triggered by (HP:0025204)

Parent Node:
Triggered by carbohydrate ingestion (HP:0025208)

..Starting node
..Triggered by glucose ingestion (HP:0025210)

Term ID:

25210

Name:

Triggered by glucose ingestion

Synonym:

Definition:

Applies to a sign or symptom that is provoked or brought about by eating or drinking glucose.

Comments:

Reference:

HP:0025210

Genes and Diseases:

Child Nodes:

Sister Nodes:

Triggered by fructose ingestion (HP:0025209)

Triggered by galactose ingestion (HP:0025213)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025210	HP:0025210	Triggered by glucose ingestion	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.