Human Phenotype Ontology 
Grandparent Node:
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Abnormal skin morphology of the palm (HP:0040211)help
Grandparent Node:
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Hyperhidrosis (HP:0000975)help
Parent Node:
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Abnormality of the plantar skin of foot (HP:0100872)help
Parent Node:
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Palmar hyperhidrosis (HP:0006089)help
..Starting node
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Palmoplantar hyperhidrosis (HP:0007410)help
Term ID: 7410
Name: Palmoplantar hyperhidrosis
Synonym: Excessive sweating of palms and soles; Hyperhidrosis of palms and soles
Definition: An abnormally increased perspiration on palms and soles.
Comments:
Reference: HP:0007410
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0007410HP:0007410Palmoplantar hyperhidrosis0COL17A1 CL E G H130879406ORPHA13922194113811
HP:0007410HP:0007410Palmoplantar hyperhidrosis0COL17A1 CL E G H130879406ORPHA14062194113811
HP:0007410HP:0007410Palmoplantar hyperhidrosis0CTSB CL E G H1508148370Keratolytic winter erythema148370C0406756OMIM11752527116810
HP:0007410HP:0007410Palmoplantar hyperhidrosis0CTSB CL E G H1508148370Keratolytic winter erythema148370C0406756OMIM11392527116810
HP:0007410HP:0007410Palmoplantar hyperhidrosis0KRT17 CL E G H3872167210Pachyonychia congenita 2167210C1721007OMIM1546427148069
HP:0007410HP:0007410Palmoplantar hyperhidrosis0KRT17 CL E G H3872167210Pachyonychia congenita 2167210C1721007OMIM1596427148069
HP:0007410HP:0007410Palmoplantar hyperhidrosis0MBTPS2 CL E G H51360659AmyoplasiaORPHA123115455300294
HP:0007410HP:0007410Palmoplantar hyperhidrosis0MBTPS2 CL E G H51360659AmyoplasiaORPHA124215455300294
HP:0007410HP:0007410Palmoplantar hyperhidrosis0RSPO1 CL E G H284654610644Palmoplantar hyperkeratosis with squamous cell carcinoma of skin and 46,XX sex reversal610644C3149931OMIM12921679609595
HP:0007410HP:0007410Palmoplantar hyperhidrosis0RSPO1 CL E G H284654610644Palmoplantar hyperkeratosis with squamous cell carcinoma of skin and 46,XX sex reversal610644C3149931OMIM13321679609595
HP:0007410HP:0007410Palmoplantar hyperhidrosis0SERPINB7 CL E G H8710615598Palmoplantar keratoderma, nagashima type615598C3810072OMIM111313902603357
HP:0007410HP:0007410Palmoplantar hyperhidrosis0SERPINB7 CL E G H8710615598Palmoplantar keratoderma, nagashima type615598C3810072OMIM110813902603357
HP:0007410HP:0007410Palmoplantar hyperhidrosis0TRPV3 CL E G H162514659AmyoplasiaORPHA133718084607066
HP:0007410HP:0007410Palmoplantar hyperhidrosis0TRPV3 CL E G H162514659AmyoplasiaORPHA132918084607066
HP:0007410HP:0007410Palmoplantar hyperhidrosis0WNT10A CL E G H80326257980Odontoonychodermal dysplasia257980C0796093OMIM130913829606268
HP:0007410HP:0007410Palmoplantar hyperhidrosis0WNT10A CL E G H80326257980Odontoonychodermal dysplasia257980C0796093OMIM129113829606268
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (8) :COL17A1 CTSB KRT17 MBTPS2 RSPO1 SERPINB7 TRPV3 WNT10A

Diseases (7) :79406 148370 167210 659 610644 615598 257980
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.