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Harlequin Type Ichthyosis
Harlequin type ichthyosis
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Harlequin syndrome
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Rare diseases
(19)
Lelis syndrome
Familial cutaneous papillomatosis
Eem syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Zunich Kaye syndrome
Ichthyosis lamellaris
Meleda Disease
Congenital ichthyosiform erythroderma
Kindler syndrome
Dermatopathia pigmentosa reticularis
Epidermolytic hyperkeratosis
Ichthyosis hystrix
Bloom syndrome
Naegeli syndrome
Ichthyosis bullosa of siemens
Hay-Wells syndrome
Netherton syndrome
Epidermolysis bullosa simplex
Multiple sulfatase deficiency
more...
Autosomal recessive disorders
(11)
Xeroderma pigmentosum
Eem syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Ichthyosis lamellaris
Ichthyosis lamellaris
Meleda Disease
Congenital ichthyosiform erythroderma
Kindler syndrome
Bloom syndrome
Netherton syndrome
Multiple sulfatase deficiency
more...
Genodermatoses
(157)
Benign familial pemphigus
Congenital ichthyosis
Epidermolysis bullosa dystrophica
Focal dermal hypoplasia
Hypohidrotic ectodermal dysplasia
Hypohidrotic ectodermal dysplasia
Ichthyosis vulgaris
Incontinentia pigmenti
Junctional epidermolysis bullosa (medicine)
Keratosis follicularis spinulosa decalvans
Neutral lipid storage disease
Pachyonychia congenita
Peeling skin syndrome
Sjogren-larsson syndrome
X-linked ichthyosis
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
Bloom syndrome
CHILD syndrome
Cardiofaci- ocutaneous syndrome
Cartilage–hair hypoplasia
Carvajal syndrome
Chondrodysplasia punctata
Cicatricial junctional epidermolysis bullosa
Clouston's hidrotic ectodermal dysplasia
Cockayne syndrome
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
Epidermolysis bullosa herpetiformis
Epidermolysis bullosa simplex
Epidermolysis bullosa simplex of Ogna
Epidermolysis bullosa simplex with mottled pigmentation
Epidermolysis bullosa simplex with muscular dystrophy
Epidermolytic hyperkeratosis
Erythrokeratodermia variabilis
Familial cutaneous papillomatosis
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
Hay-Wells syndrome
Hereditary sclerosing poikiloderma
IBIDS syndrome
IFAP syndrome
Ichthyosis bullosa of siemens
Ichthyosis hystrix
Ichthyosis lamellaris
Ichthyosis linearis circumflexa
IgA pemphigus
Incontinentia pigmenti achromians
Junctional epidermolysis bullosa gravis
Keratitisâ- €“ichthyosis–deafness syndrome
Keratolytic winter erythema
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
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
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
Xeroderma pigmentosum
Zimmermann–Laband syndrome
Zunich Kaye syndrome
more...
Diseases and disorders
(39)
Cutaneous conditions
Netherton syndrome ichthyosis
Eclabium
Ichthyosis hystrix curth macklin type
Acquired ichthyosis
Acquired ichthyosis
ICE syndrome
Skin disorder
Isotretinoin
Actinic keratosis
Alport syndrome
Acanthosis nigricans
Pemphigus vulgaris
Ectropion
Skin cancer
Eem syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Ichthyosis lamellaris
Meleda Disease
Congenital ichthyosis
Dermatopathia pigmentosa reticularis
X-linked ichthyosis
Epidermolysis bullosa dystrophica
Bloom syndrome
Benign familial pemphigus
Neutral lipid storage disease
Naegeli syndrome
Hay-Wells syndrome
Ichthyosis vulgaris
Netherton syndrome
Focal dermal hypoplasia
Epidermolysis bullosa simplex
Hypohidrotic ectodermal dysplasia
Sjogren-larsson syndrome
Keratosis follicularis spinulosa decalvans
Multiple sulfatase deficiency
Peeling skin syndrome
Incontinentia pigmenti
Xeroderma pigmentosum
more...
Syndromes
(9)
Lelis syndrome
Eem syndrome
Zunich Kaye syndrome
Bloom syndrome
Naegeli syndrome
Naegeli syndrome
Hay-Wells syndrome
Netherton syndrome
Sjogren-larsson syndrome
Alport syndrome
more...
Papulosquamous hyperkeratotic skin diseases
Familial cutaneous papillomatosis
Meleda Disease
Kindler syndrome
Pachyonychia congenita
Cutaneous conditions
Acral Acanthotic Anomaly
Acne aestivalis
Skin Conditions
Papulosquamous hyperkeratotic skin diseases
Acquired ichthyosis
Skin disorder
Pemphigus vulgaris
Genetic disorders
(21)
DNA repair-deficiency disorder
Aicardi syndrome
Hereditary disorder
Adrenoleuk- odystrophy
Lelis syndrome
Lelis syndrome
Familial cutaneous papillomatosis
Eem syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Ichthyosis lamellaris
Congenital ichthyosiform erythroderma
Kindler syndrome
Dermatopathia pigmentosa reticularis
Ichthyosis hystrix
Bloom syndrome
Ichthyosis bullosa of siemens
Hay-Wells syndrome
Netherton syndrome
Multiple sulfatase deficiency
Pachyonychia congenita
Alport syndrome
more...
See also
(20)
Nevus flammeus nuchae
Congenital malformations
Autosomal recessive
Autosomal dominant
Integument
Integument
ABCA12
Subcutaneous tissue
TGM1
Cadherin
Birthmarks
Autosomal
Lamellar
Harlequin syndrome
COL7A1
Epidermis (skin)
Acrodermatitis Chronica Atrophicans
Acantholysis
Thick Skinned
The Skin
Mutations
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