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Naegeli Syndrome
Naegeli syndrome
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Rare diseases
(18)
Lelis syndrome
Familial cutaneous papillomatosis
Eem syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Zunich Kaye syndrome
Meleda Disease
Dermatopathia pigmentosa reticularis
Ichthyosis lamellaris
Glanzmann disease
Congenital ichthyosiform erythroderma
Kindler syndrome
Hay-Wells syndrome
Bloom syndrome
Harlequin type ichthyosis
Epidermolytic palmoplantar keratoderma
Epidermolysis bullosa simplex
Netherton syndrome
Dyskeratosis congenita
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Syndromes
(9)
Thymic aplasia
Alport syndrome
Syndrome
Lelis syndrome
Eem syndrome
Eem syndrome
Zunich Kaye syndrome
Hay-Wells syndrome
Bloom syndrome
Netherton syndrome
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Genodermatoses
(157)
Ectodermal dysplasia
Epidermolysis bullosa dystrophica
Focal dermal hypoplasia
Hypohidrotic ectodermal dysplasia
Incontinentia pigmenti
Incontinentia pigmenti
Junctional epidermolysis bullosa (medicine)
Pachyonychia congenita
X-linked ichthyosis
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 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 palmoplantar keratoderma
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 achromians
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
Meleda Disease
Mitis junctional epidermolysis bullosa
Multiple sulfatase deficiency
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 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
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Diseases and disorders
(44)
Thrombasthenia of glanzmann and naegeli
Trichorhin- ophalangeal syndrome
Neuraminidase deficiency
Giant cell glioblastoma
Essential thrombocytopenia
Essential thrombocytopenia
Nevoid basal cell carcinoma syndrome
Trisomy 9
Palmoplantar keratoderma
Trisomy 22
Monilethrix
Glycogenosis
Talipes
Gastric cancer
Partial trisomy
Cutis laxa
Acanthosis nigricans
Platelet
Optic atrophy
Thyroid cancer
Skin cancer
Torn meniscus
Syndromes
Eem syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Meleda Disease
Dermatopathia pigmentosa reticularis
Ichthyosis lamellaris
Glanzmann disease
Epidermolysis bullosa dystrophica
Hay-Wells syndrome
Bloom syndrome
Harlequin type ichthyosis
Thymic aplasia
Epidermolysis bullosa simplex
Netherton syndrome
Focal dermal hypoplasia
Incontinentia pigmenti
Hypohidrotic ectodermal dysplasia
Ectodermal dysplasia
X-linked ichthyosis
Dyskeratosis congenita
Alport syndrome
Rare diseases
more...
Papulosquamous hyperkeratotic skin diseases
(57)
Punctate palmoplantar keratoderma
Acquired keratoderma
Acrokerato- elastoidosis of Costa
Aquagenic wrinkling of the palms
Arrhythmogenic right ventricular dysplasia
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
Diffuse palmoplantar keratoderma
Digitate dermatosis
Erythroderma
Erythrokeratodermia variabilis
Familial cutaneous papillomatosis
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
Keratoderma blennorrhagica
Keratoderma climactericum
Keratolysis exfoliativa
Keratosis punctata of the palmar creases
Keratosis punctata palmaris et plantaris
Kindler syndrome
Large-plaque parapsoriasis
Meleda Disease
Olmsted syndrome
Pachyonychia congenita
Pachyonychia congenita type I
Pachyonychia congenita type II
Palmoplantar keratoderma
Palmoplantar keratoderma and spastic paraplegia
Palmoplantar keratoderma of Sybert
Papillon–Lefèvre syndrome
Parapsoriasis
Pityriasis rosea
Pityriasis rubra pilaris
Porokeratosis plantaris discreta
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...
Autosomal recessive disorders
(11)
Eem syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Meleda Disease
Ichthyosis lamellaris
Ichthyosis lamellaris
Glanzmann disease
Congenital ichthyosiform erythroderma
Kindler syndrome
Bloom syndrome
Harlequin type ichthyosis
Netherton syndrome
more...
Cutaneous conditions
Acral Acanthotic Anomaly
Acne aestivalis
Papulosquamous hyperkeratotic skin diseases
Punctate palmoplantar keratoderma
Palmoplantar keratoderma
Genetic disorders
(27)
DNA repair-deficiency disorder
Tetrasomy
X-linked dominant
Lelis syndrome
Familial cutaneous papillomatosis
Familial cutaneous papillomatosis
Eem syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Dermatopathia pigmentosa reticularis
Ichthyosis lamellaris
Glanzmann disease
Congenital ichthyosiform erythroderma
Kindler syndrome
Trichorhin- ophalangeal syndrome
Hay-Wells syndrome
Bloom syndrome
Thymic aplasia
Netherton syndrome
Pachyonychia congenita
Nevoid basal cell carcinoma syndrome
Trisomy 9
Trisomy 22
Monilethrix
Dyskeratosis congenita
Alport syndrome
Partial trisomy
Hereditary disorder
more...
See also
(20)
Nevus flammeus nuchae
Congenital malformations
Autosomal recessive
Autosomal dominant
Integument
Integument
KRT14
Subcutaneous tissue
Naegeli
Birthmarks
Telecanthus
COL7A1
Keratin 1
People
Scientists
Acrodermatitis Chronica Atrophicans
Josef Jadassohn
Coagulation disorder
Am. J. Hum. Genet.
Acantholysis
Hemorrhagic
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