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:
Increased body weight (HP:0004324)

Parent Node:
Obesity (HP:0001513)

..Starting node
..Class I obesity (HP:0025499)

Term ID:

25499

Name:

Class I obesity

Synonym:

Obesity grade 1

Definition:

Obesity with a body mass index of 30 to 34.9 kg per square meter.

Comments:

Reference:

HP:0025499

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abdominal obesity (HP:0012743)

Class II obesity (HP:0025500)

Class III obesity (HP:0025501)

Truncal obesity (HP:0001956)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025499	HP:0025499	Class I obesity	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.