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Erythroderma
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Papulosquamous hyperkeratotic skin diseases
(56)
Erythrokeratodermia variabilis
Familial cutaneous papillomatosis
Florid cutaneous papillomatosis
Ichthyosiform erythroderma, corneal involvement, and deafness
Kindler syndrome
Kindler syndrome
Meleda Disease
Palmoplantar keratoderma
Pityriasis rosea
Pityriasis rubra pilaris
Acquired keratoderma
Acrokerato- elastoidosis of Costa
Aquagenic wrinkling of the palms
Arrhythmogenic right ventricular dysplasia
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
Focal acral hyperkeratosis
Focal palmoplantar keratoderma
Focal palmoplantar keratoderma with oral mucosal hyperkeratosis
Howel–Evans syndrome
Junctional epidermolysis bullosa with pyloric atresia
Keratoderma
Keratoderma blennorrhagica
Keratoderma climactericum
Keratolysis exfoliativa
Keratosis punctata of the palmar creases
Keratosis punctata palmaris et plantaris
Large-plaque parapsoriasis
Olmsted syndrome
Pachyonychia congenita
Pachyonychia congenita type I
Pachyonychia congenita type II
Palmoplantar keratoderma and spastic paraplegia
Palmoplantar keratoderma of Sybert
Papillon–Lefèvre syndrome
Parapsoriasis
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...
Dermatology
(23)
Psoriatic erythroderma
Sign of Leser-Trelat
Acral Acanthotic Anomaly
Bacterial skin disease
Ichthyosis acquisita
Ichthyosis acquisita
Pemphigoid, bullous
Acne aestivalis
Neutral lipid storage disease
Lelis syndrome
Dermatologic terminology
Granuloma faciale
Peeling skin syndrome
Ichthyosis linearis circumflexa
Erythema multiforme
Keratosis follicularis spinulosa decalvans
Trichorrhexis invaginata
Erythema elevatum diutinum
Sjogren-larsson syndrome
Ichthyosiform erythroderma, corneal involvement, and deafness
Familial cutaneous papillomatosis
Meleda Disease
Erythrokeratodermia variabilis
Palmoplantar keratoderma
more...
Medical condition
(48)
Erythroderma desquamativa of leiner
Bullous erythroderma ichthyosiformis congenita of brocq
Ichthyosis
Collodion baby
Acute lymphadenitis
Acute lymphadenitis
Erythema
Eem syndrome
Ichthyosis hystrix curth macklin type
Ichthyosis congenita
Gerodermia osteodysplastica
Actinic keratosis
Netherton syndrome
Netherton syndrome ichthyosis
Zunich Kaye syndrome
Skin disorder
Actinic cheilitis
Ichthyosis bullosa of siemens
Ibids syndrome
Impetigo
Lichen planus
X-linked ichthyosis
Acanthosis nigricans
Dermatopathia pigmentosa reticularis
Leiner disease
Benign familial pemphigus
Naegeli syndrome
Sezary syndrome
Encephalotrigeminal Angiomatosis
Erythremia
Pruritus
Pityriasis lichenoides et varioliformis acuta
Dermatitis
Ichthyosis vulgaris
Lupus erythematosus
Skeletal dysplasia
Ichthyosiform erythroderma, corneal involvement, and deafness
Ichthyosis acquisita
Pemphigoid, bullous
Neutral lipid storage disease
Meleda Disease
Peeling skin syndrome
Ichthyosis linearis circumflexa
Erythema multiforme
Pityriasis rubra pilaris
Keratosis follicularis spinulosa decalvans
Erythema elevatum diutinum
Sjogren-larsson syndrome
Palmoplantar keratoderma
more...
Rare diseases
(17)
Bullous congenital ichthyosiform erythroderma
Congenital ichthyosiform erythroderma
Ichthyosis hystrix
Multiple sulfatase deficiency
Florid cutaneous papillomatosis
Florid cutaneous papillomatosis
Collodion baby
Eem syndrome
Familial cutaneous papillomatosis
Meleda Disease
Ichthyosis congenita
Gerodermia osteodysplastica
Lelis syndrome
Netherton syndrome
Zunich Kaye syndrome
Dermatopathia pigmentosa reticularis
Kindler syndrome
Naegeli syndrome
more...
Autosomal recessive disorders
(10)
Congenital ichthyosiform erythroderma
Collodion baby
Eem syndrome
Meleda Disease
Ichthyosis congenita
Ichthyosis congenita
Gerodermia osteodysplastica
Netherton syndrome
Zunich Kaye syndrome
Kindler syndrome
Multiple sulfatase deficiency
more...
Genetic disorders
(13)
Hereditary disorder
Congenital ichthyosiform erythroderma
Collodion baby
Eem syndrome
Familial cutaneous papillomatosis
Familial cutaneous papillomatosis
Gerodermia osteodysplastica
Lelis syndrome
Netherton syndrome
Zunich Kaye syndrome
Ichthyosis hystrix
Dermatopathia pigmentosa reticularis
Kindler syndrome
Multiple sulfatase deficiency
more...
Lymphoid-related cutaneous conditions
(38)
Cutaneous T cell lymphoma
Mycosis fungoides
Angiocentric lymphoma
Angioimmunoblastic T-cell lymphoma
Blastic NK-cell lymphoma
Blastic NK-cell lymphoma
CD30+ cutaneous T-cell lymphoma
Cutaneous B-cell lymphoma
Cutaneous lymphoid hyperplasia
Cutaneous lymphoid hyperplasia with bandlike and perivascular patterns
Cutaneous lymphoid hyperplasia with nodular pattern
Cutaneous myelofibrosis
Diffuse large B cell lymphoma
Erythremia
Familial cutaneous papillomatosis
Granulomatous slack skin
Ichthyosis acquisita
Intravascular large B-cell lymphoma
Jessner lymphocytic infiltrate of the skin
Lennert lymphoma
Leukemia cutis
Leukemids
Lymphomatoid papulosis
Malignant histiocytosis
Marginal zone B-cell lymphoma
Myeloid sarcoma
Non-mycosis fungoides CD30− cutaneous large T-cell lymphoma
Pagetoid reticulosis
Pityriasis lichenoides chronica
Pityriasis lichenoides et varioliformis acuta
Plasmacytoma
Pleomorphic T-cell lymphoma
Primary cutaneous follicular lymphoma
Primary cutaneous immunocytoma
Primary cutaneous marginal zone lymphoma
Rosai-Dorfman disease
Secondary cutaneous CD30+ large cell lymphoma
Sezary syndrome
Subcutaneous T-cell lymphoma
more...
Dermatologic terminology
Acantholysis
Bullous
Keratosis
Genodermatosis
Erythema
Skin disorder
Diseases and disorders
(12)
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects
Papulosquamous disorders
Eclabium
Ichthyosis acquisita
Dermatopathia pigmentosa reticularis
Dermatopathia pigmentosa reticularis
Cutaneous T cell lymphoma
Keratosis
Naegeli syndrome
Sezary syndrome
Genodermatosis
Multiple sulfatase deficiency
Skeletal dysplasia
more...
Genodermatoses
(154)
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
Bullous congenital ichthyosiform erythroderma
Cardiofaci- ocutaneous syndrome
Cartilage–hair hypoplasia
Chondrodysplasia punctata
Cicatricial junctional epidermolysis bullosa
Clouston's hidrotic ectodermal dysplasia
Cockayne syndrome
Collodion baby
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects
Congenital ichthyosiform erythroderma
Conradi Hunermann 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
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
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
Hallerman–Streiff syndrome
Hay–Wells syndrome
Hereditary sclerosing poikiloderma
Hypohidrotic ectodermal dysplasia
IBIDS syndrome
IFAP syndrome
Ichthyosiform erythroderma, corneal involvement, and deafness
Ichthyosis
Ichthyosis bullosa of Siemens
Ichthyosis congenita
Ichthyosis hystrix
Ichthyosis linearis circumflexa
Ichthyosis vulgaris
IgA pemphigus
Incontinentia pigmenti
Incontinentia pigmenti achromians
Junctional epidermolysis bullosa (medicine)
Junctional epidermolysis bullosa gravis
Keratolytic winter erythema
Keratosis follicularis spinulosa decalvans
Keratosis pilaris
Keratosis pilaris atrophicans faciei
Kindler 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
Von Hippel – Lindau disease
Watson syndrome
Werner syndrome
Westerhof syndrome
Wilson–Turner syndrome
X-linked ichthyosis
X-linked recessive chondrodysplasia punctata
XXYY syndrome
Xeroderma pigmentosum
Zimmerman-Laband syndrome
Zunich Kaye syndrome
more...
Infectious skin disease
(8)
Lichen simplex chronicus
Nummular dermatitis
Pityriasis alba
Prurigo nodularis
Pruritus ani
Pruritus ani
Pruritus scroti
Pruritus vulvae
Seborrhoeic dermatitis
more...
See also
(20)
Integument
Subcutaneous tissue
Acrodermatitis Chronica Atrophicans
Ultraviolet
Livedoid vasculitis
Livedoid vasculitis
Dermatographic urticaria
Nevus flammeus nuchae
Congenital malformations
Keratin 1
Keratins
ALOXE3
J. Invest. Dermatol.
Cornification
ALOX12B
NSDHL
TGM1
Collodion
Autosomal recessive
Central American Integration System
KRT10
more...
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