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:
Abnormal skin morphology of the palm (HP:0040211)

Grandparent Node:
Hyperkeratosis (HP:0000962)

Parent Node:
Palmar hyperkeratosis (HP:0010765)

..Starting node
..Punctate palmar hyperkeratosis (HP:0007508)

Term ID:

7508

Name:

Punctate palmar hyperkeratosis

Synonym:

Definition:

Tiny bumps of thickened skin (hyperkeratosis) on the palms of the hands.

Comments:

Reference:

HP:0007508

Genes and Diseases:

Child Nodes:

Sister Nodes:

Palmoplantar hyperkeratosis (HP:0000972)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0007508	HP:0007508	Punctate palmar hyperkeratosis	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.