Hereditary palmoplantar keratoderma

General Information (adopted from Orphanet):

Synonyms, Signs: Hereditary palmoplantar hyperkeratosis
Hereditary keratosis palmoplantaris
Hereditary PPK
Number of Symptoms 2
OrphanetNr: 79357
OMIM Id:
ICD-10: Q82.8
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: Epidermal disease
 -Rare skin disease
Genetic epidermal disease
 -Rare genetic disease

Symptom Information: Sort by abundance 

1
 (HPO:0000962) Hyperkeratosis Very frequent [Orphanet] 216 / 7739
2
 (HPO:0001072) Thickened skin Very frequent [Orphanet] 87 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: