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Ichthyosis Vulgaris
Ichthyosis vulgaris
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Genodermatoses
(157)
Benign familial pemphigus
Bloom syndrome
Bullous Ichthyosis
Congenital ichthyosiform erythroderma
Conradi Hunermann syndrome
Conradi Hunermann syndrome
Dermatopathia pigmentosa reticularis
Erythrokeratodermia variabilis
Familial cutaneous papillomatosis
Hay-Wells syndrome
Ichthyosis
Ichthyosis bullosa of siemens
Ichthyosis congenita
Ichthyosis hystrix
Ichthyosis lamellaris
Ichthyosis linearis circumflexa
Ichthyosis, Netherton syndrome
Ifap syndrome
Incontinentia pigmenti
Junctional epidermolysis bullosa (medicine)
Keratosis follicularis spinulosa decalvans
Keratosis pilaris
Kindler syndrome
Lelis syndrome
Meleda Disease
Naegeli syndrome
Neutral lipid storage disease
Pachyonychia congenita
Peeling skin syndrome
Sjogren-larsson syndrome
X-linked ichthyosis
Xeroderma pigmentosum
Zunich Kaye syndrome
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
Cockayne syndrome
Costello syndrome
Cronkhite-Canada syndrome
Crouzon syndrome
Cutis verticis gyrata
Darier's disease
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
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
Hereditary sclerosing poikiloderma
Hypohidrotic ectodermal dysplasia
IBIDS syndrome
IgA pemphigus
Incontinentia pigmenti achromians
Junctional epidermolysis bullosa gravis
Keratitisâ- €“ichthyosis–deafness syndrome
Keratolytic winter erythema
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
Noonan syndrome
Odonto–T- richo–Ungual–Digital–Palmar syndrome
PIBI(D)S syndrome
POEMS syndrome
Pachydermo- periostosis
Pachyonychia congenita type I
Pachyonychia congenita type II
Papillon–Lefèvre 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
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
Zimmermann–Laband syndrome
more...
Diseases and disorders
(51)
IgA nephropathy
Mesangial proliferative glomerulonephritis
Intestinal pseudo-obstruction
Cutaneous conditions
Idiopathic myelofibrosis
Idiopathic myelofibrosis
Eem syndrome
Gerodermia osteodysplastica
Acquired ichthyosis
Iga deficiency
Imperforate anus
Immune thrombocytopenic purpura
Iliotibial band syndrome
Acanthosis nigricans
Keratosis
Icterus
Dermatitis
Ichthyosis male hypogonadism
Netherton syndrome ichthyosis
Lichen planus
Actinic keratosis
Eczema
Ichthyosis hystrix curth macklin type
Ichthyosis hystrix gravior
Infantile hemangioen- dothelioma
Ileal neoplasms
Dermatosis
Juvenile plantar dermatosis
ICE syndrome
Monilethrix
Infantile polyarteritis
Ectropion
Ichthyosis
Ichthyosis lamellaris
Zunich Kaye syndrome
X-linked ichthyosis
Meleda Disease
Ichthyosis congenita
Dermatopathia pigmentosa reticularis
Benign familial pemphigus
Ichthyosis linearis circumflexa
Ichthyosis, Netherton syndrome
Naegeli syndrome
Keratosis follicularis spinulosa decalvans
Bloom syndrome
Hay-Wells syndrome
Sjogren-larsson syndrome
Ifap syndrome
Xeroderma pigmentosum
Neutral lipid storage disease
Incontinentia pigmenti
Peeling skin syndrome
more...
Rare diseases
(19)
Lelis syndrome
Ichthyosis lamellaris
Familial cutaneous papillomatosis
Eem syndrome
Gerodermia osteodysplastica
Gerodermia osteodysplastica
Zunich Kaye syndrome
Congenital ichthyosiform erythroderma
Meleda Disease
Bullous Ichthyosis
Ichthyosis congenita
Ichthyosis hystrix
Dermatopathia pigmentosa reticularis
Kindler syndrome
Ichthyosis, Netherton syndrome
Naegeli syndrome
Bloom syndrome
Ichthyosis bullosa of siemens
Hay-Wells syndrome
Ifap syndrome
more...
Genetic disorders
(18)
Lelis syndrome
Ichthyosis lamellaris
Familial cutaneous papillomatosis
Eem syndrome
Gerodermia osteodysplastica
Gerodermia osteodysplastica
Zunich Kaye syndrome
Congenital ichthyosiform erythroderma
Keratosis pilaris
Ichthyosis hystrix
Dermatopathia pigmentosa reticularis
Kindler syndrome
Ichthyosis, Netherton syndrome
Bloom syndrome
Ichthyosis bullosa of siemens
Hay-Wells syndrome
Pachyonychia congenita
Ifap syndrome
Monilethrix
more...
Syndromes
(9)
Lelis syndrome
Eem syndrome
Zunich Kaye syndrome
Ichthyosis, Netherton syndrome
Naegeli syndrome
Naegeli syndrome
Bloom syndrome
Hay-Wells syndrome
Sjogren-larsson syndrome
Conradi Hunermann syndrome
more...
Dermatology
Xerosis
Stratum corneum
Keratinocytes
Cutaneous conditions
Dermatologic terminology
Hyperkeratosis
Bullous
Papules
Xerosis
Keratosis
Dermatosis
Medicine
Idiopathic
Filaggrin
Intracranial hypotension
Keratohyalin
Diseases and disorders
Ischemic hepatitis
Symptoms
Speech impairment
Idiopathic hypersomnia
Scaly skin
Scales
Xeroderma
See also
(20)
Ileus
Icterus icterus
Impaction
Nevus flammeus nuchae
Integument
Integument
Subcutaneous tissue
Impacted tooth
Imodium a-d
Congenital malformations
Scale (zoology)
Infectious diarrhea
Napoleon I of France
Atopic dermatitis
Autosomal recessive
Autosomal dominant
J. Invest. Dermatol.
Asteatotic eczema
STS (gene)
Cadherin
Abrasion (medical)
more...
more categories...
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