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:
Urethral stenosis (HP:0008661)

Parent Node:
Urethral stricture (HP:0012227)

..Starting node
..Bulbar urethral stricture (HP:0025415)

Term ID:

25415

Name:

Bulbar urethral stricture

Synonym:

Definition:

A type of urethral stricture affecting the bulbar urethra, which is the part of the urethra that traverses the root of the penis.

Comments:

Reference:

HP:0025415

Genes and Diseases:

Child Nodes:

Sister Nodes:

Fossa navicularis urethral stricture (HP:0025413)

Pendulous urethral stricture (HP:0025414)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025415	HP:0025415	Bulbar urethral stricture	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.