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X-linked Ichthyosis
X-linked ichthyosis
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Inborn errors of metabolism
Glycogen storage disease type iib
Lipid storage disorder
Adenosine deaminase deficiency
Genodermatoses
(157)
Benign familial pemphigus
Bloom syndrome
CHILD syndrome
Chondrodysplasia punctata
Congenital ichthyosiform erythroderma
Congenital ichthyosiform erythroderma
Conradi Hunermann syndrome
Dermatopathia pigmentosa reticularis
Epidermolysis bullosa dystrophica
Epidermolysis bullosa simplex
Epidermolytic hyperkeratosis
Erythrokeratodermia variabilis
Familial cutaneous papillomatosis
Focal dermal hypoplasia
Harlequin type ichthyosis
Hay-Wells syndrome
Hypohidrotic ectodermal dysplasia
Ichthyosis
Ichthyosis hystrix
Ichthyosis lamellaris
Ichthyosis vulgaris
Incontinentia pigmenti
Keratosis follicularis spinulosa decalvans
Kindler syndrome
Lelis syndrome
Meleda Disease
Multiple sulfatase deficiency
Naegeli syndrome
Netherton syndrome
Neutral lipid storage disease
Pachyonychia congenita
Peeling skin syndrome
Sjogren-larsson syndrome
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
Cardiofaci- ocutaneous syndrome
Cartilage–hair hypoplasia
Carvajal syndrome
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 herpetiformis
Epidermolysis bullosa simplex of Ogna
Epidermolysis bullosa simplex with mottled pigmentation
Epidermolysis bullosa simplex with muscular dystrophy
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
IBIDS syndrome
IFAP syndrome
Ichthyosis bullosa of Siemens
Ichthyosis linearis circumflexa
IgA pemphigus
Incontinentia pigmenti achromians
Junctional epidermolysis bullosa (medicine)
Junctional epidermolysis bullosa gravis
Keratitisâ- €“ichthyosis–deafness syndrome
Keratolytic winter erythema
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
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
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Diseases and disorders
(52)
Eem syndrome
Gerodermia osteodysplastica
MASA syndrome
Acquired ichthyosis
X-linked sideroblastic anemia
X-linked sideroblastic anemia
Netherton syndrome ichthyosis
Apparent mineralocorticoid excess syndrome
Hydrops-ectopic calcificat- ion-moth-eaten skeletal dysplasia
Becker's muscular dystrophy
Rud syndrome
Ichthyosis hystrix curth macklin type
Pyruvate dehydrogenase deficiency
Alport syndrome
X-linked lymphoproliferative disease
X-linked hypophosphatemia
Lathosterolosis
Barth syndrome
ICE syndrome
Androgen insensitivity syndrome
17 beta-hydroxysteroid dehydrogenase deficiency
Skin disorder
Kallmann syndrome
Achondrogenesis type 2
Hypogonadism
Haemophilia
Glycogen storage disease type iib
Zunich Kaye syndrome
Ichthyosis lamellaris
Meleda Disease
Ichthyosis
Harlequin type ichthyosis
Ichthyosis vulgaris
Dermatopathia pigmentosa reticularis
Lipid storage disorder
Epidermolysis bullosa dystrophica
Bloom syndrome
Focal dermal hypoplasia
Neutral lipid storage disease
Benign familial pemphigus
Naegeli syndrome
Hay-Wells syndrome
Multiple sulfatase deficiency
Netherton syndrome
Chondrodysplasia punctata
Keratosis follicularis spinulosa decalvans
Sjogren-larsson syndrome
Epidermolysis bullosa simplex
Peeling skin syndrome
Hypohidrotic ectodermal dysplasia
CHILD syndrome
Incontinentia pigmenti
Adenosine deaminase deficiency
more...
Syndromes
(14)
McLeod syndrome
Antley-bixler syndrome
Lelis syndrome
Eem syndrome
Zunich Kaye syndrome
Zunich Kaye syndrome
Bloom syndrome
Alport syndrome
Naegeli syndrome
Hay-Wells syndrome
Netherton syndrome
Conradi Hunermann syndrome
Sjogren-larsson syndrome
Androgen insensitivity syndrome
Kallmann syndrome
more...
Papulosquamous hyperkeratotic skin diseases
Familial cutaneous papillomatosis
Meleda Disease
Kindler syndrome
Erythrokeratodermia variabilis
Pachyonychia congenita
Autosomal recessive disorders
(15)
Eem syndrome
Gerodermia osteodysplastica
Glycogen storage disease type iib
Zunich Kaye syndrome
Ichthyosis lamellaris
Ichthyosis lamellaris
Meleda Disease
Congenital ichthyosiform erythroderma
Harlequin type ichthyosis
Kindler syndrome
Lipid storage disorder
Bloom syndrome
Multiple sulfatase deficiency
Netherton syndrome
Antley-bixler syndrome
Adenosine deaminase deficiency
more...
Chromosomes
Autosomal
X chromosome
Short arm
Genetics
X linked
X-linked recessive
Hereditary disorder
X inactivation
Genetic disorders
(38)
Aicardi syndrome
Hyperimmun- oglobulinemia D with recurrent fever
DNA repair-deficiency disorder
Adrenoleuk- odystrophy
X-linked dominant
X-linked dominant
Lelis syndrome
Familial cutaneous papillomatosis
Eem syndrome
Gerodermia osteodysplastica
Glycogen storage disease type iib
Zunich Kaye syndrome
Ichthyosis lamellaris
Congenital ichthyosiform erythroderma
MASA syndrome
X-linked sideroblastic anemia
Dermatopathia pigmentosa reticularis
Apparent mineralocorticoid excess syndrome
Kindler syndrome
Ichthyosis hystrix
Lipid storage disorder
Becker's muscular dystrophy
Rud syndrome
Simpson-Go- labi-Behmel syndrome
Pyruvate dehydrogenase deficiency
McLeod syndrome
Bloom syndrome
Alport syndrome
Hay-Wells syndrome
Multiple sulfatase deficiency
Netherton syndrome
Barth syndrome
Androgen insensitivity syndrome
Antley-bixler syndrome
Hereditary disorder
Kallmann syndrome
Pachyonychia congenita
Adenosine deaminase deficiency
Haemophilia
more...
See also
(20)
Nevus flammeus nuchae
Hyper IgM Syndrome Type 1
Subcutaneous tissue
STS (gene)
Congenital malformations
Congenital malformations
Autosomal recessive
Autosomal dominant
Simpson-Go- labi-Behmel syndrome
Integument
Cadherin
Birthmarks
KAL1
Steroid metabolism
Letters by alphabet
Military expedition (disambiguation)
Immune disorders
Acral Acanthotic Anomaly
Epidermis (skin)
5 alpha reductase deficiency
Arylsulfatase
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