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 spleen morphology (HP:0025408)

Parent Node:
Splenic abscess (HP:0025059)

..Starting node
..Unifocal splenic abscess (HP:0025061)

Term ID:

25061

Name:

Unifocal splenic abscess

Synonym:

Solitary splenic abscess; Unilocular splenic abscess

Definition:

Single (solitary) abscess in the spleen.

Comments:

Reference:

HP:0025061

Genes and Diseases:

Child Nodes:

Sister Nodes:

Multifocal splenic abscess (HP:0025060)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025061	HP:0025061	Unifocal splenic abscess	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.