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 obstruction (HP:0000796)

Parent Node:
Urethral stenosis (HP:0008661)

..Starting node
..Urethral sphincter sclerosis (HP:0008664)

Term ID:

8664

Name:

Urethral sphincter sclerosis

Synonym:

Definition:

Comments:

Reference:

HP:0008664

Genes and Diseases:

Child Nodes:

Sister Nodes:

Urethral stricture (HP:0012227)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0008664	HP:0008664	Urethral sphincter sclerosis	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.