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:
Recurrent infections (HP:0002719)

Parent Node:
Recurrent fungal infections (HP:0002841)

..Starting node
..Recurrent plantar mycosis (HP:0025472)

Term ID:

25472

Name:

Recurrent plantar mycosis

Synonym:

Definition:

A history of repeated fungal infections located on the sole of the foot, usually manifested by scaling, maceration, and itching.

Comments:

Reference:

HP:0025472

Genes and Diseases:

Child Nodes:

Sister Nodes:

Chronic mucocutaneous candidiasis (HP:0002728)

Onychomycosis (HP:0012203)

Recurrent Aspergillus infections (HP:0002724)

Recurrent candida infections (HP:0005401)

Recurrent interdigital mycosis (HP:0025351)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025472	HP:0025472	Recurrent plantar mycosis	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.