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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

13 clinical trials for this condition and its sub-types, 0 tagged with Hereditary palmoplantar keratoderma itself.

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Where it sits in the disease tree

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Part of

↑ Hereditary skin disorder (880) ↑ Epidermal disease (128) ↑ Palmoplantar keratosis (16)

Sub-types of Hereditary palmoplantar keratoderma

Diffuse palmoplantar keratoderma 0 trials · 12 incl. sub-types
32 sub-types
- Papillon-Lefevre disease 5 trials
- Corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome 4 trials
- Odonto-onycho-dermal dysplasia 2 trials
- Epidermolytic palmoplantar keratoderma, 1 1 trial
- Bart-Pumphrey syndrome 0 trials
- CEDNIK syndrome 0 trials
- Clouston syndrome 0 trials
- Curly hair - acral keratoderma - caries syndrome 0 trials
- Haim-Munk syndrome 0 trials
- KID syndrome 0 trials Sub-types →
- Naegeli-Franceschetti-Jadassohn syndrome 0 trials
- Schöpf-Schulz-Passarge syndrome 0 trials
- Autosomal dominant palmoplantar keratoderma and congenital alopecia 0 trials
- Autosomal recessive palmoplantar keratoderma and congenital alopecia 0 trials
- Dermatopathia pigmentosa reticularis 0 trials
- Diffuse nonepidermolytic palmoplantar keratoderma 0 trials
- Diffuse palmoplantar keratoderma - acrocyanosis syndrome 0 trials
- Diffuse palmoplantar keratoderma with painful fissures 0 trials
- Erythrokeratodermia variabilis 0 trials Sub-types →
- Hearing loss with skin disease 0 trials
- Hereditary palmoplantar keratoderma, Gamborg-Nielsen type 0 trials
- Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome 0 trials
- Keratosis palmaris et plantaris-clinodactyly syndrome 0 trials
- Loricrin keratoderma 0 trials
- Mal de Meleda 0 trials
- Palmoplantar keratoderma, Bothnian type 0 trials
- Palmoplantar keratoderma, Nagashima type 0 trials
- Palmoplantar keratoderma-XX sex reversal-predisposition to squamous cell carcinoma syndrome 0 trials
- Palmoplantar keratoderma-deafness syndrome 0 trials
- Palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome 0 trials Sub-types →
- Palmoplantar keratoderma-sclerodactyly syndrome 0 trials
- Skin fragility-woolly hair-palmoplantar keratoderma syndrome 0 trials
Olmsted syndrome 1 trial
3 sub-types
- Olmsted syndrome 1 0 trials
- Olmsted syndrome 2 0 trials
- Olmsted syndrome, X-linked 0 trials
Focal palmoplantar keratoderma 0 trials · 1 incl. sub-types
12 sub-types
- Pachyonychia congenita 1 trial Sub-types →
- Focal palmoplantar and gingival keratoderma 0 trials
- Focal palmoplantar keratoderma with joint keratoses 0 trials
- Hereditary painful callosities 0 trials
- Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome 0 trials
- Isolated focal non-epidermolytic palmoplantar keratoderma 0 trials
- Nail and teeth abnormalities-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome 0 trials
- Palmoplantar keratoderma, nonepidermolytic, focal 1 0 trials
- Palmoplantar keratoderma-esophageal carcinoma syndrome 0 trials
- Striate palmoplantar keratoderma 0 trials Sub-types →
- Tyrosinemia type II 0 trials
- Wooly hair-palmoplantar keratoderma syndrome 0 trials
Palmoplantar keratoderma, epidermolytic 0 trials · 1 incl. sub-types
2 sub-types
- Epidermolytic palmoplantar keratoderma, 1 1 trial
- Palmoplantar keratoderma, epidermolytic, 2 0 trials
Alopecia congenita keratosis palmoplantaris 0 trials
Palmoplantar keratoderma i, striate, focal, or diffuse 0 trials
Palmoplantar keratoderma, nonepidermolytic, focal or diffuse 0 trials
Punctate palmoplantar keratoderma 0 trials
4 sub-types
- Focal acral hyperkeratosis 0 trials
- Punctate palmoplantar keratoderma type 1 0 trials Sub-types →
- Punctate palmoplantar keratoderma type 2 0 trials
- Punctate palmoplantar keratoderma type III 0 trials

Most studied deeper sub-types

Autosomal dominant keratitis-ichthyosis-hearing loss syndrome (0) Erythrokeratodermia variabilis et progressiva 1 (0) Erythrokeratodermia variabilis et progressiva 2 (0) Erythrokeratodermia variabilis et progressiva 3 (0) Erythrokeratodermia variabilis et progressiva 4 (0) Erythrokeratodermia variabilis et progressiva 5 (0) Erythrokeratodermia variabilis et progressiva 6 (0) Erythrokeratodermia variabilis et progressiva 7 (0) Ichthyosiform erythroderma, corneal involvement, and hearing loss (0) Ichthyosis, hystrix-like, with hearing loss (0) Keratosis palmoplantaris striata 2 (0) Keratosis palmoplantaris striata 3 (0) Pachyonychia congenita 1 (0) Pachyonychia congenita 2 (0) Pachyonychia congenita 3 (0) Pachyonychia congenita 4 (0) Palmoplantar keratoderma, punctate type 1A (0) Palmoplantar keratoderma, punctate type ib (0) Palmoplantar keratoderma-spastic paralysis syndrome (0) Transgrediens et progrediens palmoplantar keratoderma (0)

Including sub-types (13) Tagged with Hereditary palmoplantar keratoderma (0)

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