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 penis morphology (HP:0000036)

Parent Node:
Abnormal preputium morphology (HP:0100587)

..Starting node
..Paraphimosis (HP:0100588)

Term ID:

100588

Name:

Paraphimosis

Synonym:

Definition:

The foreskin becomes trapped behind the glans penis, and cannot be pulled back to its normal flaccid position covering the glans penis.

Comments:

Reference:

HP:0100588

Genes and Diseases:

Child Nodes:

Sister Nodes:

Congenital absence of foreskin (HP:0012421)

Phimosis (HP:0001741)

Ventral shortening of foreskin (HP:0012435)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100588	HP:0100588	Paraphimosis	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.