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Epidermolysis Bullosa Dystrophica
Epidermolysis bullosa dystrophica
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Genodermatoses
(157)
Aplasia cutis congenita
Bloom syndrome
Congenital ichthyosiform erythroderma
Congenital ichthyosis
Dermatopathia pigmentosa reticularis
Dermatopathia pigmentosa reticularis
Dominant dystrophic epidermolysis bullosa
Dyskeratosis congenita
Dystrophic Epidermolysis Bullosa
Epidermolysis bullosa simplex
Epidermolytic hyperkeratosis
Familial cutaneous papillomatosis
Harlequin type ichthyosis
Hay-Wells syndrome
Hypohidrotic ectodermal dysplasia
Ichthyosis bullosa of siemens
Ichthyosis lamellaris
Junctional epidermolysis bullosa (medicine)
Kindler syndrome
Lelis syndrome
Meleda Disease
Naegeli syndrome
Netherton syndrome
Recessive dystrophic epidermolysis bullosa
X-linked ichthyosis
Zunich Kaye syndrome
18q deletion syndrome
Acrocephal- osyndactylia
Acrodermatitis enteropathica
Acrokeratosis verruciformis
Adams–Oliver syndrome
Adducted thumbs syndrome
Albright's hereditary osteodystrophy
Apert syndrome
Arrhythmogenic right ventricular dysplasia
Ataxia telangiectasia
Atrichia with papular lesions
Atrophodermia vermiculata
Autoimmune polyendocr- inopathy–candidiasis–ectodermal dystrophy syndrome
BIDS syndrome
Bart syndrome
CHILD syndrome
Cardiofaci- ocutaneous syndrome
Cartilage–hair hypoplasia
Carvajal syndrome
Chondrodysplasia punctata
Cicatricial junctional epidermolysis bullosa
Clouston's hidrotic ectodermal dysplasia
Cockayne syndrome
Conradi–Hünermann syndrome
Costello syndrome
Cronkhite-Canada syndrome
Crouzon syndrome
Cutis verticis gyrata
Darier's disease
Disseminated superficial actinic porokeratosis
Disseminated superficial porokeratosis
Dyschromatosis universalis hereditaria
Ectodermal dysplasia
Ectodermal dysplasia with corkscrew hairs
Ectrodacty- ly-ectodermal dysplasia-cleft syndrome
Epidermolysis bullosa herpetiformis
Epidermolysis bullosa simplex of Ogna
Epidermolysis bullosa simplex with mottled pigmentation
Epidermolysis bullosa simplex with muscular dystrophy
Erythrokeratodermia variabilis
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
Hailey-Hailey disease
Hallermann-Streiff syndrome
Hereditary sclerosing poikiloderma
IBIDS syndrome
IFAP syndrome
Ichthyosis hystrix
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
Klinefelter's syndrome
Klippel–Feil syndrome
LEOPARD 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
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
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
more...
Diseases and disorders
(41)
Eem syndrome
Gerodermia osteodysplastica
Achondrogenesis type 2
Schmid metaphyseal chondrodysplasia
Bethlem myopathy
Bethlem myopathy
Ehlers Danlos Syndrome
Pelger-Huet anomaly
Marshall syndrome
Hypochondrogenesis
Alport syndrome
Epidermolysis bullosa junctional
Raine syndrome
Fibrochondrogenesis
Multiple epiphyseal dysplasia
Steatocystoma multiplex
Bullous pemphigoid
Epidermolysis bullosa acquisita
Osteochondropathy
Osteochond- rodysplasia
Chondromatous
Stickler syndrome
Cutis laxa
Acanthosis nigricans
Pemphigus vulgaris
Achondroplasia
Skin cancer
Zunich Kaye syndrome
Ichthyosis lamellaris
Meleda Disease
Dermatopathia pigmentosa reticularis
Hay-Wells syndrome
Naegeli syndrome
Bloom syndrome
Epidermolysis bullosa simplex
Harlequin type ichthyosis
Netherton syndrome
Aplasia cutis congenita
X-linked ichthyosis
Congenital ichthyosis
Hypohidrotic ectodermal dysplasia
Dyskeratosis congenita
more...
Syndromes
(15)
Laminopathy
Buschke-Ollendorff syndrome
Barraquer-Simons Syndrome
Lelis syndrome
Eem syndrome
Eem syndrome
Zunich Kaye syndrome
Ehlers Danlos Syndrome
Marshall syndrome
Hay-Wells syndrome
Naegeli syndrome
Bloom syndrome
Alport syndrome
Raine syndrome
Netherton syndrome
Stickler syndrome
more...
Autosomal recessive disorders
(13)
Atelosteogenesis, type II
Eem syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Ichthyosis lamellaris
Ichthyosis lamellaris
Meleda Disease
Kindler syndrome
Congenital ichthyosiform erythroderma
Bloom syndrome
Harlequin type ichthyosis
Raine syndrome
Fibrochondrogenesis
Netherton syndrome
more...
Abnormalities of dermal fibrous and elastic tissue
(19)
Acrodermatitis Chronica Atrophicans
Anetoderma
Blepharochalasis
Cutis laxa
Ehlers Danlos Syndrome
Ehlers Danlos Syndrome
Elastosis perforans serpiginosa
Gerodermia osteodysplastica
Homocystinuria
Linear focal elastosis
Marfan syndrome
Osteogenesis imperfecta
Perforating calcific elastosis
Pseudoxanthoma elasticum
Reactive perforating collagenosis
Stretch marks
Striae distensae
Ullrich disease
Verrucous perforating collagenoma
Wrinkly skin syndrome
more...
Structural proteins
(26)
Anchoring fibrils
Scleroprotein
Type I collagen
Type II collagen
Type-VII collagen
Type-VII collagen
Actin
Amyloid
Catenin
Claudin
Coilin
Collagen, type III, alpha 1
Collagen, type XVII, alpha 1
Elastic fiber
Elastin
Elaunin
Extensin
Fibrillin
Fibrillogenesis
Hydrolyzed collagen
Keratins
Lamin
Osteolathyrism
ParM
Reticular fiber
Sclerotin
Spongin
more...
Congenital disorders
Congenital malformations
Achondrogenesis type 1B
Achondrogenesis type 2
Buschke-Ollendorff syndrome
Bethlem myopathy
Ehlers Danlos Syndrome
Fibrochondrogenesis
Cutaneous conditions
Papulosquamous hyperkeratotic skin diseases
Acral Acanthotic Anomaly
Acne aestivalis
Bullous pemphigoid
Epidermolysis bullosa acquisita
Pemphigus vulgaris
Human body
Keratinopathy
Subcutaneous tissue
Type-VII collagen
Genetic disorders
(33)
Collagenopathy, types II and XI
DNA repair-deficiency disorder
Aicardi syndrome
Adrenoleuk- odystrophy
Lelis syndrome
Lelis syndrome
Familial cutaneous papillomatosis
Eem syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Ichthyosis lamellaris
Laminopathy
Buschke-Ollendorff syndrome
Barraquer-Simons Syndrome
Kindler syndrome
Congenital ichthyosiform erythroderma
Ichthyosis bullosa of siemens
Bethlem myopathy
Dermatopathia pigmentosa reticularis
Ehlers Danlos Syndrome
Pelger-Huet anomaly
Marshall syndrome
Hypochondrogenesis
Hay-Wells syndrome
Bloom syndrome
Alport syndrome
Raine syndrome
Fibrochondrogenesis
Multiple epiphyseal dysplasia
Atelosteogenesis, type II
Netherton syndrome
Dyskeratosis congenita
Stickler syndrome
Achondroplasia
more...
See also
(20)
Nevus flammeus nuchae
Autosomal dominant
Autosomal recessive
COL7A1
Integument
Integument
Birthmark (band)
COL2A1 gene
Julian Voss-Andreae
Lamina densa
The Proteolysis Map
Autoimmune
Epidermis (skin)
Acantholysis
Fibrillar
Microfibril
J. Mol. Biol.
Cadherin
Integrin
Leslie Orgel
Gly
more...
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