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Hereditary palmoplantar keratoderma

MONDO:0019272

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

Also known as: hereditary PPK, hereditary keratosis palmoplantaris, hereditary palmoplantar hyperkeratosis, hereditary palmoplantar keratosis

18 clinical trials for this condition and its sub-types.

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Sub-types

Papillon-Lefevre disease (4) Corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome (3) Odonto-onycho-dermal dysplasia (2) Epidermolytic palmoplantar keratoderma, 1 (1) Olmsted syndrome (1) Pachyonychia congenita (1) Alopecia congenita keratosis palmoplantaris (0) Autosomal dominant keratitis-ichthyosis-hearing loss syndrome (0) Autosomal dominant palmoplantar keratoderma and congenital alopecia (0) Autosomal recessive palmoplantar keratoderma and congenital alopecia (0) Bart-Pumphrey syndrome (0) CEDNIK syndrome (0) Clouston syndrome (0) Curly hair - acral keratoderma - caries syndrome (0) Dermatopathia pigmentosa reticularis (0) Diffuse nonepidermolytic palmoplantar keratoderma (0) Diffuse palmoplantar keratoderma (0) Diffuse palmoplantar keratoderma - acrocyanosis syndrome (0) Diffuse palmoplantar keratoderma with painful fissures (0) Erythrokeratodermia variabilis (0)

Broader categories

Disease (618) Hereditary disease (172) Skin disorder (123) Human disease (14) Hereditary skin disorder (5) Palmoplantar keratosis (4) Keratosis (3) Disease of genetic or genomic mechanism (2) Disease by body system or component (0) Disease by developmental or physiological process (0)
Trials to join now! 8 Not yet recruiting 5 Not yet finished but already full! 3 Completed 2
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