Human Phenotype Ontology 
Grandparent Node:
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Abnormal foot morphology (HP:0001760)help
Grandparent Node:
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Regional abnormality of skin (HP:0011356)help
Parent Node:
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Abnormal dermatoglyphics (HP:0007477)help
Parent Node:
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Abnormal skin morphology of the palm (HP:0040211)help
Parent Node:
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Abnormality of the plantar skin of foot (HP:0100872)help
..Starting node
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Palmoplantar cutis gyrata (HP:0007469)help
Term ID: 7469
Name: Palmoplantar cutis gyrata
Synonym: Cutis gyrata of palms and soles
Definition: Cutis gyrata of palms and soles.
Comments:
Reference: HP:0007469
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal plantar dermatoglyphics (HP:0010506) help
..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 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:0007469HP:0007469Palmoplantar cutis gyrata0B4GALT7 CL E G H11285930ORPHA:75496B4GALT7-related spondylodysplastic Ehlers-Danlos syndromeHP:0040281 - Very frequent29
HP:0007469HP:0007469Palmoplantar cutis gyrata0B4GALT7 CL E G H11285930OMIM:130070Ehlers-Danlos syndrome, spondylodysplastic type, 1.29
HP:0007469HP:0007469Palmoplantar cutis gyrata0FGFR2 CL E G H22633689ORPHA:1555Cutis gyrata-acanthosis nigricans-craniosynostosis syndromeHP:0040281 - Very frequent175


Genes (2) :B4GALT7 FGFR2

Diseases (3) :ORPHA:75496 OMIM:130070 ORPHA:1555
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.