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:
Hyperkeratosis (HP:0000962)

Parent Node:
Palmoplantar keratoderma (HP:0000982)

..Starting node
..obsolete Congenital palmoplantar keratodermia (HP:0007597)

Term ID:

7597

Name:

obsolete Congenital palmoplantar keratodermia

Synonym:

Definition:

Comments:

Reference:

HP:0007597

Genes and Diseases:

Child Nodes:

Sister Nodes:

Honeycomb palmoplantar hyperkeratosis (HP:0007465)

Nonepidermolytic palmoplantar hyperkeratosis (HP:0007404)

obsolete Diffuse palmoplantar keratoderma (HP:0007435)

Patchy palmoplantar hyperkeratosis (HP:0005588)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0007597	HP:0007597	obsolete Congenital palmoplantar keratodermia	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.