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Cockayne Syndrome
Cockayne syndrome
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Genodermatoses
(157)
Acrocephal- osyndactylia
Apert syndrome
Ataxia telangiectasia
Crow-Fukase syndrome
Epidermolysis bullosa
Epidermolysis bullosa
Epidermolysis bullosa simplex
Junctional epidermolysis bullosa (medicine)
Progeria
Refsum syndrome
Trichothiodystrophy
Weber-Cockayne syndrome
Werner syndrome
Windmill-Vane-Hand syndrome
Xeroderma pigmentosum
Zimmerman Laband syndrome
18q deletion syndrome
Acrodermatitis enteropathica
Acrokeratosis verruciformis
Adams–Oliver syndrome
Adducted thumbs syndrome
Albright's hereditary osteodystrophy
Aplasia cutis congenita
Arrhythmogenic right ventricular dysplasia
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
Confluent and reticulated papillomatosis of Gougerot and Carteaud
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 dystrophica
Epidermolysis bullosa herpetiformis
Epidermolysis bullosa simplex of Ogna
Epidermolysis bullosa simplex with mottled pigmentation
Epidermolysis bullosa simplex with muscular dystrophy
Epidermolytic hyperkeratosis
Erythrokeratodermia variabilis
Focal dermal hypoplasia
Focal palmoplantar keratoderma with oral mucosal hyperkeratosis
Follicular atrophoderma
Franceschetti–Klein 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
Hypohidrotic ectodermal dysplasia
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 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
Mandibuloacral dysplasia
Marinesco–Sjögren syndrome
McCusick syndrome
Meleda disease
Mitis junctional epidermolysis bullosa
Multiple sulfatase deficiency
Naegeli–- Franceschetti–Jadassohn 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
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
Progressive symmetric erythrokeratodermia
Proteus syndrome
Punctate porokeratosis
Rapp–Hodgkin syndrome
Recessive dystrophic epidermolysis bullosa
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
Westerhof syndrome
Wilson–Turner syndrome
Wolf–Hirschhorn syndrome
X-linked ichthyosis
X-linked recessive chondrodysplasia punctata
XXYY syndrome
Zunich–Kaye syndrome
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Autosomal recessive disorders
(13)
Adducted thumb syndrome
Werdnig-Hoffmann disease
Ablepharon macrostomia syndrome
Fountain syndrome
Wilsons disease
Wilsons disease
Keutel syndrome
Yunis Varon syndrome
Donohue syndrome
Carpenter syndrome
Cerebrotendinous xanthomatosis
Fraser syndrome
Xeroderma pigmentosum
Werner syndrome
more...
Neurological disorders
Wernicke-Korsakoff syndrome
Timothy syndrome
Charcot-Marie Tooth Disease
Wilsons disease
Crow-Fukase syndrome
Rare diseases
(22)
Williams syndrome
Urban Rogers Meyer syndrome
Aarskog-Scott syndrome
Cerebrohepatorenal syndrome
Multiple system atrophy
Multiple system atrophy
Robinow syndrome
Cowden syndrome
Multiple hereditary exostoses
Adducted thumb syndrome
Zimmerman Laband syndrome
Ablepharon macrostomia syndrome
Fountain syndrome
Wilsons disease
Keutel syndrome
Yunis Varon syndrome
Donohue syndrome
Werner syndrome
Epidermolysis bullosa
Progeria
Carpenter syndrome
Crow-Fukase syndrome
Epidermolysis bullosa simplex
more...
Syndromes
(22)
Wolff Parkinson White syndrome
Waterhouse- -friderichsen syndrome
Silver-Russell dwarfism
Waardenburg-Shah syndrome
Sotos syndrome
Sotos syndrome
Williams syndrome
Adducted thumb syndrome
Urban Rogers Meyer syndrome
Zimmerman Laband syndrome
Ablepharon macrostomia syndrome
Aarskog-Scott syndrome
Fountain syndrome
Keutel syndrome
Yunis Varon syndrome
Donohue syndrome
Wernicke-Korsakoff syndrome
Werner syndrome
Apert syndrome
Carpenter syndrome
Windmill-Vane-Hand syndrome
Crow-Fukase syndrome
Robinow syndrome
more...
Genetic disorders
(38)
Sakati-Nyh- an-Tisdale syndrome
Branchio-Oto-Renal Syndrome
Laurence Moon syndrome
DNA repair-deficiency disorder
Bardet Biedl Syndrome
Bardet Biedl Syndrome
Crouzonode- rmoskeletal syndrome
Glutaricaciduria
Beckwith wiedemann syndrome
Vacterl association
Wermer Syndrome
Coffin-lowry syndrome
Wolff Parkinson White syndrome
Williams syndrome
Adducted thumb syndrome
Urban Rogers Meyer syndrome
Werdnig-Hoffmann disease
Zimmerman Laband syndrome
Ablepharon macrostomia syndrome
Acrocephal- osyndactylia
Aarskog-Scott syndrome
Fountain syndrome
Wilsons disease
Keutel syndrome
Yunis Varon syndrome
Donohue syndrome
Werner syndrome
Progeria
Timothy syndrome
Apert syndrome
Cerebrohepatorenal syndrome
Ataxia telangiectasia
Charcot-Marie Tooth Disease
Carpenter syndrome
Robinow syndrome
Waardenburg-Shah syndrome
Cerebrotendinous xanthomatosis
Fraser syndrome
Multiple hereditary exostoses
more...
Diseases and disorders
(73)
Wilms tumor
Wryneck
Windburn
West nile fever
Weil disease
Weil disease
Waldenstroms
Wolfram syndrome
Macroglobulinemia
Granulomatosis
Weariness
Craniofrontonasal dysplasia
Weaver syndrome
Chromosome 5p- syndrome
Mohr syndrome
Chromosome 9 trisomy
Cystathionine beta-synthase deficiency disease
Congenital arthromyodysplasia
Floating harbor syndrome
Cutis laxa recessive
Chromosome 5 trisomy 5p
Wilms tumor and pseudoherm- aphroditism
Epidermolysis bullosa acquisita
Metaphyseal dysplasia
Wiedemann rautenstrauch syndrome
Weismann netter stuhl syndrome
Water on the brain
Wildervanck syndrome
Seckel syndrome
Juvenile primary lateral sclerosis
Myotonic dystrophy type 2
Wolff Parkinson White syndrome
Sakati-Nyh- an-Tisdale syndrome
Adducted thumb syndrome
Urban Rogers Meyer syndrome
Werdnig-Hoffmann disease
Xeroderma pigmentosum
Ablepharon macrostomia syndrome
Acrocephal- osyndactylia
Aarskog-Scott syndrome
Fountain syndrome
Wilsons disease
Keutel syndrome
Yunis Varon syndrome
Donohue syndrome
Wernicke-Korsakoff syndrome
Werner syndrome
Branchio-Oto-Renal Syndrome
Progeria
Timothy syndrome
Apert syndrome
Bardet Biedl Syndrome
Trichothiodystrophy
Cerebrohepatorenal syndrome
Ataxia telangiectasia
Charcot-Marie Tooth Disease
Carpenter syndrome
Glutaricaciduria
Beckwith wiedemann syndrome
Vacterl association
Windmill-Vane-Hand syndrome
Refsum syndrome
Multiple system atrophy
Crow-Fukase syndrome
Epidermolysis bullosa simplex
Robinow syndrome
Waardenburg-Shah syndrome
Cerebrotendinous xanthomatosis
Sotos syndrome
Cowden syndrome
Wermer Syndrome
Coffin-lowry syndrome
Fraser syndrome
Multiple hereditary exostoses
more...
Short stature
Cornelia de Lange Syndrome
Dubowitz syndrome
Smith-Lemli-Opitz syndrome
Silver-Russell dwarfism
Robinow syndrome
Noonan syndrome
Turner syndrome
Inborn error of metabolism
Fanconi anemia
Li-Fraumeni syndrome
Nijmegen breakage syndrome
Severe combined immunodeficiency
Werner syndrome
Rothmund–Thomson syndrome
See also
(20)
Walking pneumonia
Whipple procedure
Cockayne
Edward Alfred Cockayne
DNA repair
DNA repair
Winded
ERCC6 (gene)
Accelerated aging
Autosomal recessive
Economics
TFIIH
Biogerontology
CAMFAK syndrome
Degenerative disease
Genetic disorder
ERCC8
Autosomal dominant
Nucleotide excision repair
Water deprivation test
Transcription coupled repair
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