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 joint morphology (HP:0001367)

Parent Node:
Arthralgia (HP:0002829)

Parent Node:
Arthritis (HP:0001369)

..Starting node
..Arthralgia/arthritis (HP:0005059)

Term ID:

5059

Name:

Arthralgia/arthritis

Synonym:

Joint pain/Joint inflammation

Definition:

Comments:

Reference:

HP:0005059

Genes and Diseases:

Child Nodes:

Sister Nodes:

Gout (HP:0001997)

Oligoarthritis (HP:0040313)

Osteoarthritis (HP:0002758)

Rheumatoid arthritis (HP:0001370)

Septic arthritis (HP:0003095)

Sterile arthritis (HP:0040310)

Symmetric polyarthritis (HP:0040311)

Temporomandibular arthritis (HP:0040312)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0005059	HP:0005059	Arthralgia/arthritis	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.