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:
Abnormality of the scrotum (HP:0000045)

Parent Node:
Abnormal scrotal rugation (HP:0012856)

..Starting node
..Decreased scrotal rugation (HP:0012858)

Term ID:

12858

Name:

Decreased scrotal rugation

Synonym:

Definition:

Decreased number or density of the folded ridges (wrinkles) of skin of the scrotum.

Comments:

Reference:

HP:0012858

Genes and Diseases:

Child Nodes:

Sister Nodes:

Increased scrotal rugation (HP:0012857)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012858	HP:0012858	Decreased scrotal rugation	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.