Human Phenotype Ontology 
Grandparent Node:
expandAbnormal foot morphology (HP:0001760)help
Grandparent Node:
expandRegional abnormality of skin (HP:0011356)help
Parent Node:
expandAbnormal dermatoglyphics (HP:0007477)help
Parent Node:
expandAbnormality of the plantar skin of foot (HP:0100872)help
..Starting node
..expandAbnormal plantar dermatoglyphics (HP:0010506)help
Term ID: 10506
Name: Abnormal plantar dermatoglyphics
Synonym: Abnormal dermatoglyphics on feet; Abnormal prints on feet
Definition: An abnormality of dermatoglyphs on the toes and soles, i.e., an abnormality of the patterns of ridges of the skin of sole of foot.
Comments:
Reference: HP:0010506
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandConvex contour of sole (HP:0011303) help
..expandDeep plantar creases (HP:0001869) help
..expandHypertrophy of skin of soles (HP:0007403) help
..expandMultiple plantar creases (HP:0008113) help
..expandPalmoplantar blistering (HP:0007446) help
..expandPalmoplantar cutis gyrata (HP:0007469) help
..expandPalmoplantar cutis laxa (HP:0007517) help
..expandPalmoplantar hyperhidrosis (HP:0007410) help
..expandPlantar edema (HP:0025537) help
..expandPlantar hyperkeratosis (HP:0007556) help
..expandPlantar pits (HP:0010612) help
..expandPlantar telangiectasia (HP:0100870) 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:0010506HP:0010506Abnormal plantar dermatoglyphics0 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.