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Netherton Syndrome
Netherton syndrome
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Rare diseases
(18)
Lelis syndrome
Familial cutaneous papillomatosis
Eem syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Zunich Kaye syndrome
Ichthyosis lamellaris
Meleda Disease
Congenital ichthyosiform erythroderma
Dermatopathia pigmentosa reticularis
Kindler syndrome
Leukodystrophy, globoid cell
Bullous Ichthyosis
Hay-Wells syndrome
Naegeli syndrome
Ichthyosis hystrix
Bloom syndrome
Harlequin type ichthyosis
Epidermolysis bullosa simplex
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Autosomal recessive disorders
(10)
Eem syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Ichthyosis lamellaris
Meleda Disease
Meleda Disease
Congenital ichthyosiform erythroderma
Kindler syndrome
Leukodystrophy, globoid cell
Bloom syndrome
Harlequin type ichthyosis
more...
Syndromes
(11)
Hereditary sensory and autonomic neuropathies
Fetofetal transfusion
Conradi Hunermann syndrome
Sjogren-larsson syndrome
Craniofacial dysostosis
Craniofacial dysostosis
Lelis syndrome
Eem syndrome
Zunich Kaye syndrome
Hay-Wells syndrome
Naegeli syndrome
Bloom syndrome
more...
Genodermatoses
(157)
Benign familial pemphigus
Epidermolysis bullosa dystrophica
Erythrokeratodermia variabilis
Ichthyosis
Ichthyosis linearis circumflexa
Ichthyosis linearis circumflexa
Keratosis follicularis spinulosa decalvans
Neutral lipid storage disease
Pachyonychia congenita
Peeling skin syndrome
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
Bullous Ichthyosis
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 Hunermann syndrome
Costello syndrome
Craniofacial dysostosis
Cronkhite-Canada 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
Familial cutaneous papillomatosis
Focal dermal hypoplasia
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
Hallermann-Streiff syndrome
Harlequin type ichthyosis
Hay-Wells syndrome
Hereditary sclerosing poikiloderma
Hypohidrotic ectodermal dysplasia
IBIDS syndrome
IFAP syndrome
Ichthyosis bullosa of Siemens
Ichthyosis hystrix
Ichthyosis lamellaris
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 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
Naegeli syndrome
Neurofibromatosis
Neurofibromatosis type 3
Neurofibromatosis type 4
Neurofibromatosis type I
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
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
Sjogren-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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Genetic disorders
(21)
Hyperostosis, cortical, congenital
Adrenoleuk- odystrophy
DNA repair-deficiency disorder
Galactosemias
Monilethrix
Monilethrix
Lelis syndrome
Familial cutaneous papillomatosis
Eem syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Ichthyosis lamellaris
Congenital ichthyosiform erythroderma
Dermatopathia pigmentosa reticularis
Kindler syndrome
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Hay-Wells syndrome
Ichthyosis hystrix
Bloom syndrome
Craniofacial dysostosis
Pachyonychia congenita
more...
Diseases and disorders
(78)
Netherton syndrome ichthyosis
Cutaneous conditions
Congenital hypomyelination
Chromosome 9 trisomy
Chromosome 5 trisomy 5p
Chromosome 5 trisomy 5p
Glossopharyngeal nerve diseases
Purpura, schoenlein-henoch
Type i complex regional pain syndrome
Camptomelic syndrome
Myopathies, structural, congenital
Chromosome 9 tetrasomy 9p
Enterocolitis, pseudomembranous
Histiocytosis non-langerhans-cell
Nakamura osame syndrome
Nanism due to growth hormone combined deficiency
Narrow oral fissure short stature cone shaped epiphyses
Nephronophthisis familial adult spastic quadriparesis
Nephropathy deafness hyperparathyroidism
Nephropathy familial with hyperuricemia
Nephrosis deafness urinary tract digital malformation
Nephrotic syndrome ocular anomalies
Neuhauser eichner opitz syndrome
Neuraminidase beta-galactosidase deficiency
Neuroaxonal dystrophy renal tubular acidosis
Neuroma biliary tract
Neuronal interstitial dysplasia
Neuropathy motor sensory type 2 deafness mental retardation
Neuropathy sensory spastic paraplegia
Neutropenia intermittent
Neutropenia monocytopenia deafness
Night blindness skeletal anomalies unusual facies
Noble bass sherman syndrome
Non-lissencephalic cortical dysplasia
Noninsulin- -dependent diabetes mellitus with deafness
Nose polyposis familial
Novak syndrome
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Postpoliomyelitis syndrome
Encephalitis, arbovirus
Olfaction disorders
Physiologic nystagmus
Ichthyosis hystrix curth macklin type
N-acetyl-g- lucosamine-6-sulfate sulfatase deficiency
Intervertebral disk displacement
Rosenthal syndrome
Erythroderma
Brachial plexus neuropathies
Optic neuropathy, ischemic
Genodermatosis
Skin disorder
Eem syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Ichthyosis lamellaris
Meleda Disease
Ichthyosis linearis circumflexa
Dermatopathia pigmentosa reticularis
Hyperostosis, cortical, congenital
Epidermolysis bullosa dystrophica
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Fetofetal transfusion
X-linked ichthyosis
Neutral lipid storage disease
Peeling skin syndrome
Hay-Wells syndrome
Naegeli syndrome
Bloom syndrome
Benign familial pemphigus
Harlequin type ichthyosis
Ichthyosis
Galactosemias
Monilethrix
Sjogren-larsson syndrome
Craniofacial dysostosis
Epidermolysis bullosa simplex
Keratosis follicularis spinulosa decalvans
more...
Papulosquamous hyperkeratotic skin diseases
(57)
Acquired keratoderma
Acrokerato- elastoidosis of Costa
Aquagenic wrinkling of the palms
Arrhythmogenic right ventricular dysplasia
Camisa disease
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
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...
Conditions of the skin appendages
Trichorrhexis invaginata
Trichorrhexis nodosa
Monilethrix
Pachyonychia congenita
See also
(13)
Nevus flammeus nuchae
Congenital malformations
SPINK5
Autosomal recessive
Autosomal dominant
Autosomal dominant
Integument
Subcutaneous tissue
Birthmarks
Netherton, Wakefield
Cornification
Autosomal
Epidermis (skin)
The International League of Dermatological Societies
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