Human Phenotype Ontology 
Grandparent Node:
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Palmar hyperkeratosis (HP:0010765)help
Grandparent Node:
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Plantar hyperkeratosis (HP:0007556)help
Parent Node:
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Palmoplantar hyperkeratosis (HP:0000972)help
..Starting node
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Spinous keratoses of palms and soles (HP:0007613)help
Term ID: 7613
Name: Spinous keratoses of palms and soles
Synonym:
Definition:
Comments:
Reference: HP:0007613
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCongenital palmoplantar hyperkeratosis (HP:0007545) help
..expandCongenital symmetrical palmoplantar keratosis (HP:0007553) help
..expandDiffuse palmoplantar hyperkeratosis (HP:0007447) help
..expandFocal friction-related palmoplantar hyperkeratosis (HP:0007497) help
..expandobsolete Palmoplantar keratosis with erythema and scale (HP:0007548) help
..expandPunctate palmoplantar hyperkeratosis (HP:0007530) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0007613HP:0007613Spinous keratoses of palms and soles0 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.