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:
Hair follicle neoplasm (HP:0012843)

Parent Node:
Trichilemmoma (HP:0012844)

..Starting node
..Multiple trichilemmomata (HP:0012846)

Term ID:

12846

Name:

Multiple trichilemmomata

Synonym:

Multiple trichilemmomas

Definition:

Presence of multiple trichilemmomata, a benign tumour originating from the outer root sheath of the hair follicle.

Comments:

Reference:

HP:0012846

Genes and Diseases:

Child Nodes:

Sister Nodes:

Single trichilemmoma (HP:0012845)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012846	HP:0012846	Multiple trichilemmomata	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.