Palmoplantar keratosis
MONDO:0006590A group of autosomal dominant, autosomal recessive, X-linked inherited or acquired disorders characterized by the thickening of the palms and soles due to hyperkeratosis.
Also known as: palmoplantar keratoderma, keratoderma, palmoplantar
15 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome
(4)
Papillon-Lefevre disease
(4)
Odonto-onycho-dermal dysplasia
(2)
Aquagenic palmoplantar keratoderma
(1)
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)