Kosmix
One sec... we're building your guide for
Netherton Syndrome Ichthyosis
Netherton syndrome ichthyosis
Overview
Health Providers & Organizations
Tools
Main ›
Tools
›
Skinsight
Body Location Disease Search
Related in the Kosmos
?
Diseases and disorders
(77)
Cutaneous conditions
Eem syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Meleda Disease
Meleda Disease
Ichthyosis lamellaris
Dermatopathia pigmentosa reticularis
Glossopharyngeal nerve diseases
Hyperostosis, cortical, congenital
Purpura, schoenlein-henoch
Type i complex regional pain syndrome
Myopathies, structural, congenital
Ichthyosis linearis circumflexa
Congenital hypomyelination
Chromosome 9 trisomy
Chromosome 5 trisomy 5p
Enterocolitis, pseudomembranous
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Physiologic nystagmus
Fetofetal transfusion
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
Ichthyosis hystrix curth macklin type
Epidermolysis bullosa dystrophica
Camptomelic syndrome
N-acetyl-g- lucosamine-6-sulfate sulfatase deficiency
X-linked ichthyosis
Intervertebral disk displacement
Chromosome 9 tetrasomy 9p
Rosenthal syndrome
Naegeli syndrome
Bloom syndrome
Neutral lipid storage disease
Benign familial pemphigus
Peeling skin syndrome
Harlequin type ichthyosis
Galactosemias
Hay-Wells syndrome
Brachial plexus neuropathies
Optic neuropathy, ischemic
Ichthyosis
Erythroderma
Genodermatosis
Sjogren-larsson syndrome
Skin disorder
Epidermolysis bullosa simplex
Multiple sulfatase deficiency
Craniofacial dysostosis
Cutis laxa
more...
Rare diseases
(19)
Lelis syndrome
Familial cutaneous papillomatosis
Congenital ichthyosiform erythroderma
Kindler syndrome
Ichthyosis hystrix
Ichthyosis hystrix
Epidermolytic hyperkeratosis
Eem syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Meleda Disease
Ichthyosis lamellaris
Dermatopathia pigmentosa reticularis
Leukodystrophy, globoid cell
Naegeli syndrome
Bloom syndrome
Harlequin type ichthyosis
Hay-Wells syndrome
Epidermolysis bullosa simplex
Multiple sulfatase deficiency
more...
Syndromes
(11)
Conradi Hunermann syndrome
Lelis syndrome
Eem syndrome
Zunich Kaye syndrome
Hereditary sensory and autonomic neuropathies
Hereditary sensory and autonomic neuropathies
Fetofetal transfusion
Naegeli syndrome
Bloom syndrome
Hay-Wells syndrome
Sjogren-larsson syndrome
Craniofacial dysostosis
more...
Papulosquamous hyperkeratotic skin diseases
Erythrokeratodermia variabilis
Familial cutaneous papillomatosis
Meleda Disease
Kindler syndrome
Erythroderma
Autosomal recessive disorders
(11)
Eem syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Meleda Disease
Ichthyosis lamellaris
Ichthyosis lamellaris
Congenital ichthyosiform erythroderma
Kindler syndrome
Leukodystrophy, globoid cell
Bloom syndrome
Harlequin type ichthyosis
Multiple sulfatase deficiency
more...
Abnormalities of dermal fibrous and elastic tissue
Acrodermatitis Chronica Atrophicans
Gerodermia osteodysplastica
Cutis laxa
Cutaneous conditions
Acral Acanthotic Anomaly
Acne aestivalis
Papulosquamous hyperkeratotic skin diseases
Erythroderma
Skin disorder
Genodermatoses
(158)
18q deletion syndrome
Acrocephal- osyndactylia
Acrodermatitis enteropathica
Acrokeratosis verruciformis
Adams–Oliver syndrome
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
Benign familial pemphigus
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 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 dystrophica
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 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
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
Meleda Disease
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
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 ichthyosis
X-linked recessive chondrodysplasia punctata
XXYY syndrome
Xeroderma pigmentosum
Zimmermann–Laband syndrome
Zunich Kaye syndrome
more...
Genetic disorders
(21)
Adrenoleuk- odystrophy
DNA repair-deficiency disorder
Hereditary disorder
Lelis syndrome
Familial cutaneous papillomatosis
Familial cutaneous papillomatosis
Eem syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Ichthyosis lamellaris
Congenital ichthyosiform erythroderma
Dermatopathia pigmentosa reticularis
Hyperostosis, cortical, congenital
Kindler syndrome
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Bloom syndrome
Galactosemias
Hay-Wells syndrome
Ichthyosis hystrix
Multiple sulfatase deficiency
Craniofacial dysostosis
more...
See also
(10)
Nevus flammeus nuchae
Autosomal recessive
Autosomal dominant
SPINK5
Integument
Integument
Subcutaneous tissue
Birthmarks
Congenital malformations
Trichorrhexis invaginata
Cornification
more...
more categories...
Health Providers & Organizations
›
Vitals.com
