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Epidermolysis Bullosa Simplex
Epidermolysis bullosa simplex
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Genodermatoses
(157)
Bloom syndrome
Cockayne syndrome
Congenital ichthyosiform erythroderma
Dermatopathia pigmentosa reticularis
Dominant dystrophic epidermolysis bullosa
Dominant dystrophic epidermolysis bullosa
Dowling-Meara epidermolysis bullosa simplex
Epidermolysis bullosa
Epidermolysis bullosa dystrophica
Epidermolysis bullosa simplex with mottled pigmentation
Epidermolysis bullosa simplex with muscular dystrophy
Epidermolytic hyperkeratosis
Familial cutaneous papillomatosis
Generalized atrophic benign epidermolysis bullosa
Harlequin type ichthyosis
Hay-Wells syndrome
Ichthyosis bullosa of siemens
Ichthyosis lamellaris
Kindler syndrome
Lelis syndrome
Localized epidermolysis bullosa simplex
Meleda Disease
Naegeli-Fr- anceschetti-Jadassohn syndrome
Recessive dystrophic epidermolysis bullosa
Xeroderma pigmentosum
Zunich Kaye syndrome
epidermolysis bullosa letalis
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
CHILD syndrome
Cardiofaci- ocutaneous syndrome
Cartilage–hair hypoplasia
Carvajal syndrome
Chondrodysplasia punctata
Cicatricial junctional epidermolysis bullosa
Clouston's hidrotic ectodermal dysplasia
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
Dyskeratosis congenita
Ectodermal dysplasia
Ectodermal dysplasia with corkscrew hairs
Ectrodacty- ly-ectodermal dysplasia-cleft syndrome
Epidermolysis bullosa simplex of Ogna
Erythrokeratodermia variabilis
Focal dermal hypoplasia
Focal palmoplantar keratoderma with oral mucosal hyperkeratosis
Follicular atrophoderma
Franceschetti–Klein syndrome
Freeman-Sheldon syndrome
Generalized epidermolysis bullosa simplex
Generalized trichoepithelioma
Hailey-Hailey disease
Hallermann-Streiff syndrome
Hereditary sclerosing poikiloderma
Hypohidrotic ectodermal dysplasia
IBIDS syndrome
IFAP syndrome
Ichthyosis
Ichthyosis hystrix
Ichthyosis linearis circumflexa
Ichthyosis vulgaris
IgA pemphigus
Incontinentia pigmenti
Incontinentia pigmenti achromians
Junctional epidermolysis bullosa (medicine)
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
Mandibuloacral dysplasia
Marinesco–Sjögren syndrome
McCusick syndrome
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
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 ichthyosis
X-linked recessive chondrodysplasia punctata
XXYY syndrome
Zimmermann–Laband syndrome
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Rare diseases
(20)
Eem syndrome
Gerodermia osteodysplastica
Barraquer-Simons Syndrome
Marshall syndrome
Epidermolysis bullosa
Epidermolysis bullosa
Lelis syndrome
Familial cutaneous papillomatosis
Zunich Kaye syndrome
Meleda Disease
Ichthyosis lamellaris
Cockayne syndrome
Congenital ichthyosiform erythroderma
Dermatopathia pigmentosa reticularis
Kindler syndrome
Ichthyosis bullosa of siemens
Naegeli-Fr- anceschetti-Jadassohn syndrome
Hay-Wells syndrome
Epidermolytic hyperkeratosis
Bloom syndrome
Harlequin type ichthyosis
more...
Diseases and disorders
(36)
Epidermolysis bullosa simplex koebner type
Esophageal atresia
Eosinophilic granuloma
Epidermolysis bullosa acquisita
Epidermolysis bullosa herpetiformis dowling-meara
Epidermolysis bullosa herpetiformis dowling-meara
Achondrogenesis type 2
Schmid metaphyseal chondrodysplasia
Acantholysis bullosa
Lichen planus
Pelger-Huet anomaly
Bethlem myopathy
Epidermolysis bullosa junctional
Acanthosis nigricans
Skin disorder
Transient acantholytic dermatosis
Ehlers Danlos Syndrome
Hypochondrogenesis
Swallowing difficulties
Hereditary-sensory and autonomic neuropathy type iii
Spongioblastoma
Actinic keratosis
Epidermolysis bullosa simplex with mottled pigmentation
Eem syndrome
Gerodermia osteodysplastica
Epidermolysis bullosa dystrophica
Zunich Kaye syndrome
Meleda Disease
Ichthyosis lamellaris
Cockayne syndrome
Dermatopathia pigmentosa reticularis
Naegeli-Fr- anceschetti-Jadassohn syndrome
Marshall syndrome
Hay-Wells syndrome
Bloom syndrome
Harlequin type ichthyosis
Xeroderma pigmentosum
more...
Congenital disorders
Buschke-Ollendorff syndrome
Congenital malformations
Esophageal atresia
Achondrogenesis type 2
Bethlem myopathy
Ehlers Danlos Syndrome
Syndromes
(12)
Laminopathy
Lelis syndrome
Eem syndrome
Zunich Kaye syndrome
Cockayne syndrome
Cockayne syndrome
Buschke-Ollendorff syndrome
Barraquer-Simons Syndrome
Naegeli-Fr- anceschetti-Jadassohn syndrome
Marshall syndrome
Hay-Wells syndrome
Ehlers Danlos Syndrome
Bloom syndrome
more...
Structural proteins
(26)
Anchoring fibrils
Keratins
Scleroprotein
Type-VII collagen
Actin
Actin
Amyloid
Catenin
Claudin
Coilin
Collagen, type III, alpha 1
Collagen, type XVII, alpha 1
Elastic fiber
Elastin
Elaunin
Extensin
Fibrillin
Fibrillogenesis
Hydrolyzed collagen
Lamin
Osteolathyrism
ParM
Reticular fiber
Sclerotin
Spongin
Type-I collagen
Type-II collagen
more...
Keratins
(31)
Cytokeratin
KRT14
KRT5
Keratinopathy
Beta-keratin
Beta-keratin
Hair keratin
Keratin 1
Keratin 10
Keratin 12
Keratin 13
Keratin 15
Keratin 16
Keratin 17
Keratin 18
Keratin 19
Keratin 20
Keratin 21
Keratin 2A
Keratin 3
Keratin 4
Keratin 6A
Keratin 6B
Keratin 6C
Keratin 7
Keratin 8
Keratin 9
Tonofibril
Type I hair keratin
Type I keratin
Type II hair keratin
Type II keratin
more...
Skin anatomy
Epidermis (skin)
Hemidesmosomes
Lamina lucida
Dominance (genetics)
Autosomal dominant
Recessive
Dominance (genetics) (Co-dominance)
Dominance (genetics) (Codominance)
Dominance (genetics) (Dominant Negative)
Dominance (genetics) (Incomplete dominance)
See also
(20)
Extradural hematoma
Epikeratophakia
Epiphysiodesis
Erythroplasia of Queyrat
Plantar reflex
Plantar reflex
Erythema toxicum
Eyelid drooping
Nevus flammeus nuchae
Enterobius vermicularis
Integument
Subcutaneous tissue
J. Invest. Dermatol.
Sulforaphane
COL7A1
Plectin
Mycosis fungoides
Bullous
Bulla (genus)
Hum. Mutat.
Meesmann juvenile epithelial corneal dystrophy
more...
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