Incoming and outgoing links Palmoplantar keratoses (overview)
Back to articleIncoming links
- Anhidrotic ectodermal dysplasia
- Autosomal recessive ichthyosis lamellosa with transglutaminase deficiency
- Basal cell nevus syndrome
- Berlin syndrome
- Brünauer syndrome
- Capdepont, m.
- Costello syndrome
- DSP Gene
- Ectodermal dysplasia
- Ectodermal dysplasia-skin fragility syndrome
- Epidermolysis bullosa simplex generalized intermediaries (köbner)
- Erythrokeratodermia progressive, type burns
- Finger ankle pads real
- Fischer syndrome
- GJB2 Gene
- Hand dermatitis chronic
- Hyperkeratosis palmaris et plantaris
- Ichthyosis lamellosa and congenital (with preserved transglutaminase activity)
- Ichthyosis, Spastic Quadriplegia, and Impaired Intellectual Development
- Juvenile dermatomyositis
- Keratin
- Keratodermia climacterica
- Keratodermia palmoplantare
- Keratoelastoidosis marginalis
- Keratoma palmare et planttare hereditarium
- Keratosis follicularis acneiformis, Siemens type
- Keratosis palmaris et plantaris cum surditate congenita et leuconychia totalis unguium
- Keratosis, palmoplantar
- Keratosis palmoplantaris cum degeneratione granulosa
- Keratosis palmoplantaris diffusa with mutations in cathepsin c
- Keratosis palmoplantaris diffusa with mutations in KRT 9
- Keratosis palmoplantaris striata with mutations in desmoglein 1
- Keratosis palmoplantaris transgrediens et progrediens with mutations in slurp1
- Keratosis palmoplantaris with esophageal carcinoma
- Keratosis palmoplantaris with hypotrichosis
- Keratosis palmoplantaris with scleratrophy
- Lelis syndrome
- Naegeli-franceschetti-jadassohn syndrome
- Oculocutaneous tyrosinemia
- Olmsted syndrome
- Osteochondrodysplasia with hypertrichosis
- Pachydermoperiosteosis, primary
- Pachyonychia congenita
- Pachyonychia congenita (type I) with mutation in KRT16/6a (Jadassohn-Lewandowski)
- Palmoplantar keratoderma congenital alopecia syndrome
- Palmoplantar keratoses
- Palmoplantar keratosis type nagashima
- Plakoglobin
- Poikiloderma, congenital with warty hyperkeratosis
- Punctate palmoplantar keratoderma
- Punctured palmoplantar keratosis type 3
- Schaefer syndrome
- Schöpf-schulz-passarge syndrome
- Spanlang-tappeiner syndrome
Outgoing links
- Aquagene palmoplantar keratoderma
- Ectodermal dysplasia-skin fragility syndrome
- Hyperhidrosis (overview)
- Hyperkeratoses
- Keratosis linearis-ichthyosis congenita-keratoderma with mutations in pomp
- Keratosis palmaris et plantaris cum surditate congenita et leuconychia totalis unguium
- Keratosis palmoplantaris diffusa with mutations in cathepsin c
- Keratosis palmoplantaris diffusa with mutations in KRT 9
- Keratosis palmoplantaris striata with mutations in desmoglein 1
- Keratosis palmoplantaris transgrediens et progrediens with mutations in slurp1
- Keratosis palmoplantaris with esophageal carcinoma
- Keratosis palmoplantaris with hypopigmentation
- Keratosis palmoplantaris with hypotrichosis
- Keratosis palmoplantaris with mutations in desmoplakin
- Keratosis palmoplantaris with mutations in plakoglobin
- Keratosis palmoplantaris with spiky keratoses
- Keratosis palmoplantaris with watch glass nails and bone hypertrophy
- Koilonychie
- KRT14 Gene
- KRT6B Gene
- Loricrin keratoderm
- Naegeli-franceschetti-jadassohn syndrome
- Oculocutaneous tyrosinemia
- Olmsted syndrome
- Pachyonychia congenita
- Palmoplantar keratoses (overview)
- Poikiloderma with neutropenia
- Pseudoainhum syndrome
- Psoriasis palmaris et plantaris (overview)
- Punctate palmoplantar keratoderma
- Punctured palmoplantar keratosis type 3
- Schöpf-schulz-passarge syndrome
- Sebostasis
- Sézary syndrome