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Hereditary palmoplantar keratoderma

rare

An instance of palmoplantar keratosis that is caused by an inherited modification of the individual's genome.

Identifiers: MONDO:0019272 Orphanet:79357
Part of: Epidermal disease Hereditary skin disorder Palmoplantar keratosis
Also known as: hereditary keratosis palmoplantaris · hereditary palmoplantar hyperkeratosis · hereditary palmoplantar keratosis · hereditary PPK

Subtypes

All diseases Rare only

Disease	ID	Subtypes	Genes
Diffuse palmoplantar keratoderma	MONDO:0017666	44
Focal palmoplantar keratoderma	MONDO:0017672	18
Punctate palmoplantar keratoderma	MONDO:0017675	6
Olmsted syndrome	MONDO:0031421	3
Palmoplantar keratoderma, epidermolytic	MONDO:0968949	2
Alopecia congenita keratosis palmoplantaris	MONDO:0022417
Palmoplantar keratoderma i, striate, focal, or diffuse	MONDO:0007859		DSG1
Palmoplantar keratoderma, nonepidermolytic, focal or diffuse	MONDO:0014327		KRT6C

Rare disease

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