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 male internal genitalia morphology (HP:0000022)

Parent Node:
Abnormal prostate morphology (HP:0008775)

..Starting node
..Benign prostatic hyperplasia (HP:0008711)

Term ID:

8711

Name:

Benign prostatic hyperplasia

Synonym:

Benign prostatic hypertrophy

Definition:

The presence of non-malignant hyperplasia of the prostate.

Comments:

Reference:

HP:0008711

Genes and Diseases:

Child Nodes:

Sister Nodes:

Hypoplasia of the prostate (HP:0008687)

Prominent prostate median bar (HP:0008742)

Prostate neoplasm (HP:0100787)

Prostatitis (HP:0000024)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0008711	HP:0008711	Benign prostatic hyperplasia	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.