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Meleda Disease
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Papulosquamous hyperkeratotic skin diseases
(56)
Diffuse palmoplantar keratoderma
Familial cutaneous papillomatosis
Keratoderma
Kindler syndrome
Pachyonychia congenita
Pachyonychia congenita
Palmoplantar keratoderma
Acquired keratoderma
Acrokerato- elastoidosis of Costa
Aquagenic wrinkling of the palms
Arrhythmogenic right ventricular dysplasia
Camisa disease
Cardiofaci- ocutaneous syndrome
Clouston's hidrotic ectodermal dysplasia
Complex keratoderma
Corneodermatosseous syndrome
Darier's disease
Diffuse epidermolytic palmoplantar keratoderma
Diffuse nonepidermolytic palmoplantar keratoderma
Digitate dermatosis
Erythroderma
Erythrokeratodermia variabilis
Florid cutaneous papillomatosis
Focal acral hyperkeratosis
Focal palmoplantar keratoderma
Focal palmoplantar keratoderma with oral mucosal hyperkeratosis
Howel–Evans syndrome
Junctional epidermolysis bullosa with pyloric atresia
Keratitisâ- €“ichthyosis–deafness syndrome
Keratoderma blennorrhagica
Keratoderma climactericum
Keratolysis exfoliativa
Keratosis punctata of the palmar creases
Keratosis punctata palmaris et plantaris
Large-plaque parapsoriasis
Olmsted syndrome
Pachyonychia congenita type I
Pachyonychia congenita type II
Palmoplantar keratoderma and spastic paraplegia
Palmoplantar keratoderma of Sybert
Papillon–Lefèvre syndrome
Parapsoriasis
Pityriasis rosea
Pityriasis rubra pilaris
Porokeratosis plantaris discreta
Punctate palmoplantar keratoderma
Schöpf–- Schulz–Passarge syndrome
Scleroatrophic syndrome of Huriez
Simple keratoderma
Small-plaque parapsoriasis
Spiny keratoderma
Striate keratoderma
Striate palmoplantar keratoderma
Striate palmoplantar keratoderma, woolly hair, and left ventricular dilated cardiomyopathy
Syndromic keratoderma
Tyrosinemia type II
Vohwinkel syndrome
more...
Rare diseases
(17)
Lelis syndrome
Eem syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Ichthyosis lamellaris
Ichthyosis lamellaris
Congenital ichthyosiform erythroderma
Dermatopathia pigmentosa reticularis
Naegeli syndrome
Bloom syndrome
Hay-Wells syndrome
Harlequin type ichthyosis
Multiple sulfatase deficiency
Epidermolysis bullosa simplex
Netherton syndrome
Epidermolytic hyperkeratosis
Familial cutaneous papillomatosis
Kindler syndrome
more...
Autosomal recessive disorders
(10)
Eem syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Ichthyosis lamellaris
Congenital ichthyosiform erythroderma
Congenital ichthyosiform erythroderma
Kindler syndrome
Bloom syndrome
Harlequin type ichthyosis
Multiple sulfatase deficiency
Netherton syndrome
more...
Genodermatoses
(157)
Epidermolysis bullosa dystrophica
Focal dermal hypoplasia
Hypohidrotic ectodermal dysplasia
X-linked ichthyosis
18q deletion syndrome
18q deletion syndrome
Acrocephal- osyndactylia
Acrodermatitis enteropathica
Acrokeratosis verruciformis
Adams–Oliver syndrome
Adducted thumbs syndrome
Albright's hereditary osteodystrophy
Apert syndrome
Aplasia cutis congenita
Arrhythmogenic right ventricular dysplasia
Ataxia telangiectasia
Atrichia with papular lesions
Atrophodermia vermiculata
Autoimmune polyendocr- inopathy–candidiasis–ectodermal dystrophy syndrome
BIDS syndrome
Bart syndrome
Bloom syndrome
CHILD syndrome
Cardiofaci- ocutaneous syndrome
Cartilage–hair hypoplasia
Carvajal syndrome
Chondrodysplasia punctata
Cicatricial junctional epidermolysis bullosa
Clouston's hidrotic ectodermal dysplasia
Cockayne syndrome
Congenital ichthyosiform erythroderma
Conradi–Hünermann syndrome
Costello syndrome
Cronkhite-Canada syndrome
Crouzon syndrome
Cutis verticis gyrata
Darier's disease
Dermatopathia pigmentosa reticularis
Disseminated superficial actinic porokeratosis
Disseminated superficial porokeratosis
Dominant dystrophic epidermolysis bullosa
Dyschromatosis universalis hereditaria
Dyskeratosis congenita
Ectodermal dysplasia
Ectodermal dysplasia with corkscrew hairs
Ectrodacty- ly-ectodermal dysplasia-cleft syndrome
Epidermolysis bullosa
Epidermolysis bullosa herpetiformis
Epidermolysis bullosa simplex
Epidermolysis bullosa simplex of Ogna
Epidermolysis bullosa simplex with mottled pigmentation
Epidermolysis bullosa simplex with muscular dystrophy
Epidermolytic hyperkeratosis
Erythrokeratodermia variabilis
Familial cutaneous papillomatosis
Focal palmoplantar keratoderma with oral mucosal hyperkeratosis
Follicular atrophoderma
Franceschetti–Klein syndrome
Freeman-Sheldon syndrome
Generalized atrophic benign epidermolysis bullosa
Generalized epidermolysis bullosa simplex
Generalized trichoepithelioma
Hailey-Hailey disease
Hallermann-Streiff syndrome
Harlequin type ichthyosis
Hay-Wells syndrome
Hereditary sclerosing poikiloderma
IBIDS syndrome
IFAP syndrome
Ichthyosis
Ichthyosis bullosa of Siemens
Ichthyosis hystrix
Ichthyosis lamellaris
Ichthyosis linearis circumflexa
Ichthyosis vulgaris
IgA pemphigus
Incontinentia pigmenti
Incontinentia pigmenti achromians
Junctional epidermolysis bullosa (medicine)
Junctional epidermolysis bullosa gravis
Keratitisâ- €“ichthyosis–deafness syndrome
Keratolytic winter erythema
Keratosis follicularis spinulosa decalvans
Keratosis pilaris
Keratosis pilaris atrophicans faciei
Kindler syndrome
Klinefelter's syndrome
Klippel–Feil syndrome
LEOPARD syndrome
Lelis syndrome
Lentiginosis
Lenz–Majewski syndrome
Linear Darier disease
Linear and whorled nevoid hypermelanosis
Linear porokeratosis
Localized epidermolysis bullosa simplex
Mandibuloacral dysplasia
Marinesco–Sjögren syndrome
McCusick syndrome
Mitis junctional epidermolysis bullosa
Multiple sulfatase deficiency
Naegeli syndrome
Netherton syndrome
Neurofibromatosis
Neurofibromatosis type 3
Neurofibromatosis type 4
Neurofibromatosis type I
Neutral lipid storage disease
Noonan syndrome
Odonto–T- richo–Ungual–Digital–Palmar syndrome
PIBI(D)S syndrome
POEMS syndrome
Pachydermo- periostosis
Pachyonychia congenita
Pachyonychia congenita type I
Pachyonychia congenita type II
Papillon–Lefèvre syndrome
Peeling skin syndrome
Pfeiffer syndrome
Pityriasis rotunda
Plaque-type porokeratosis
Polyostotic fibrous dysplasia
Popliteal pterygium syndrome
Porokeratosis
Porokeratosis palmaris et plantaris disseminata
Progeria
Progressive symmetric erythrokeratodermia
Proteus syndrome
Punctate porokeratosis
Rapp–Hodgkin syndrome
Recessive dystrophic epidermolysis bullosa
Refsum's disease
Relapsing linear acantholytic dermatosis
Restrictive dermopathy
Rhizomelic chondrodysplasia punctata
Rombo syndrome
Rothmund–Thomson syndrome
Scleroatrophic syndrome of Huriez
Sjögren–Larsson syndrome
Tooth and nail syndrome
Transient bullous dermolysis of the newborn
Treacher Collins syndrome
Tricho–r- hino–phalangeal syndrome
Tuberous sclerosis
Turner syndrome
Ulerythema
Ulnar–mammary syndrome
Von Hippel – Lindau disease
Watson syndrome
Werner syndrome
Westerhof syndrome
Wilson–Turner syndrome
Wolf–Hirschhorn syndrome
X-linked recessive chondrodysplasia punctata
XXYY syndrome
Xeroderma pigmentosum
Zimmermann–Laband syndrome
Zunich Kaye syndrome
more...
Diseases and disorders
(31)
Fukuyama type muscular dystrophy
Metatropic dwarfism
Morvan disease
Marinesco sjogren syndrome
Myotubular myopathy
Myotubular myopathy
Alport syndrome
Macular degeneration, age-related
Acanthosis nigricans
Aplasia
Skin disorder
Skin cancer
Myelodysplastic syndromes
Mental retardation
Meniscus tear
Eem syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Ichthyosis lamellaris
Dermatopathia pigmentosa reticularis
Epidermolysis bullosa dystrophica
Naegeli syndrome
Bloom syndrome
Hay-Wells syndrome
Harlequin type ichthyosis
Multiple sulfatase deficiency
Focal dermal hypoplasia
Epidermolysis bullosa simplex
X-linked ichthyosis
Netherton syndrome
Hypohidrotic ectodermal dysplasia
Palmoplantar keratoderma
more...
Genetic disorders
(18)
DNA repair-deficiency disorder
Monosomy
Lelis syndrome
Familial cutaneous papillomatosis
Eem syndrome
Eem syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Ichthyosis lamellaris
Congenital ichthyosiform erythroderma
Dermatopathia pigmentosa reticularis
Kindler syndrome
Fukuyama type muscular dystrophy
Bloom syndrome
Hay-Wells syndrome
Multiple sulfatase deficiency
Pachyonychia congenita
Netherton syndrome
Alport syndrome
more...
Cutaneous conditions
Acral Acanthotic Anomaly
Acne aestivalis
Papulosquamous hyperkeratotic skin diseases
Diffuse palmoplantar keratoderma
Keratoderma
Palmoplantar keratoderma
Skin disorder
See also
(20)
Nevus flammeus nuchae
Autosomal recessive
Autosomal dominant
Integument
Subcutaneous tissue
Subcutaneous tissue
Birthmarks
Mullerian duct
Congenital malformations
Islands
Meleda
Acrodermatitis Chronica Atrophicans
Places
Skin lesion
Acantholysis
Mycosis fungoides
Cadherin
The Skin
PMID
PDQ (game show)
Mutations
more...
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