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Hypohidrotic Ectodermal Dysplasia
Hypohidrotic ectodermal dysplasia
Overview
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Related in the Kosmos
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Genodermatoses
(157)
Bloom syndrome
Congenital ichthyosiform erythroderma
Dermatopathia pigmentosa reticularis
Dyskeratosis congenita
Ectodermal dysplasia
Ectodermal dysplasia
Eec syndrome
Epidermolysis bullosa dystrophica
Epidermolysis bullosa simplex
Epidermolytic hyperkeratosis
Familial cutaneous papillomatosis
Focal dermal hypoplasia
Harlequin type ichthyosis
Hay-Wells syndrome
Hidrotic ectodermal dysplasia
Ichthyosis lamellaris
Incontinentia pigmenti
Kindler syndrome
Lelis syndrome
Meleda Disease
Naegeli syndrome
Pachyonychia congenita
Rapp-hodgkin syndrome
X-linked ichthyosis
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
Cockayne syndrome
Conradi–Hünermann 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
Ectodermal dysplasia with corkscrew hairs
Epidermolysis bullosa
Epidermolysis bullosa herpetiformis
Epidermolysis bullosa simplex of Ogna
Epidermolysis bullosa simplex with mottled pigmentation
Epidermolysis bullosa simplex with muscular dystrophy
Erythrokeratodermia variabilis
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
Hailey-Hailey disease
Hallermann-Streiff syndrome
Hereditary sclerosing poikiloderma
IBIDS syndrome
IFAP syndrome
Ichthyosis
Ichthyosis bullosa of Siemens
Ichthyosis hystrix
Ichthyosis linearis circumflexa
Ichthyosis vulgaris
IgA pemphigus
Incontinentia pigmenti achromians
Junctional epidermolysis bullosa (medicine)
Junctional epidermolysis bullosa gravis
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
Localized epidermolysis bullosa simplex
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 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
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
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 recessive chondrodysplasia punctata
XXYY syndrome
Xeroderma pigmentosum
Zimmermann–Laband syndrome
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Diseases and disorders
(46)
Syndromes
Eem syndrome
Gerodermia osteodysplastica
Glycogen storage disease type iib
Ectodermal dysplasia anhidrotic
Ectodermal dysplasia anhidrotic
MASA syndrome
X-linked sideroblastic anemia
Hypohidrosis
Becker's muscular dystrophy
Alport syndrome
Lipid storage disorder
Hyperprolinemia
Pyruvate dehydrogenase deficiency
X-linked hypophosphatemia
X-linked lymphoproliferative disease
Barth syndrome
Hereditary motor sensory neuropathy
Androgen insensitivity syndrome
Anodontia
Genodermatosis
Dysostosis
Achondrogenesis type 2
Amelogenesis imperfecta
Hypotrichosis
Adenosine deaminase deficiency
22q11.2 deletion syndrome
Actinic keratosis
Cutis laxa
Hemochromatosis
Hypophosphatasia
Ectodermal dysplasia
Zunich Kaye syndrome
Ichthyosis lamellaris
Meleda Disease
Epidermolysis bullosa dystrophica
Hay-Wells syndrome
Dermatopathia pigmentosa reticularis
Focal dermal hypoplasia
Naegeli syndrome
Bloom syndrome
Hidrotic ectodermal dysplasia
Incontinentia pigmenti
Harlequin type ichthyosis
Epidermolysis bullosa simplex
X-linked ichthyosis
Dyskeratosis congenita
more...
Syndromes
(11)
McLeod syndrome
Lelis syndrome
Eem syndrome
Zunich Kaye syndrome
Hay-Wells syndrome
Hay-Wells syndrome
Alport syndrome
Naegeli syndrome
Bloom syndrome
Androgen insensitivity syndrome
Eec syndrome
22q11.2 deletion syndrome
more...
Papulosquamous hyperkeratotic skin diseases
Familial cutaneous papillomatosis
Meleda Disease
Kindler syndrome
Hidrotic ectodermal dysplasia
Pachyonychia congenita
Autosomal recessive disorders
(13)
Eem syndrome
Gerodermia osteodysplastica
Glycogen storage disease type iib
Zunich Kaye syndrome
Ichthyosis lamellaris
Ichthyosis lamellaris
Meleda Disease
Congenital ichthyosiform erythroderma
Kindler syndrome
Lipid storage disorder
Bloom syndrome
Hyperprolinemia
Harlequin type ichthyosis
Adenosine deaminase deficiency
more...
Congenital disorders
Congenital malformations
Holoprosencephaly
Achondrogenesis type 2
Protein
X-linked hypohidrotic ectodermal dysplasia
IKBKG
ED1
Scleroprotein
Human body
Subcutaneous tissue
Sweat glands
Retinal cone
Maxilla
Mandible
Genetics
X linked
X-linked recessive
Mutations
Hereditary disorder
Genetic disorders
(34)
Aicardi syndrome
Adrenoleuk- odystrophy
X-linked dominant
Lelis syndrome
Familial cutaneous papillomatosis
Familial cutaneous papillomatosis
Eem syndrome
Gerodermia osteodysplastica
Glycogen storage disease type iib
Zunich Kaye syndrome
Ichthyosis lamellaris
MASA syndrome
X-linked sideroblastic anemia
Congenital ichthyosiform erythroderma
Hay-Wells syndrome
Kindler syndrome
Dermatopathia pigmentosa reticularis
Becker's muscular dystrophy
Alport syndrome
Lipid storage disorder
Simpson-Go- labi-Behmel syndrome
Bloom syndrome
Hyperprolinemia
Pyruvate dehydrogenase deficiency
McLeod syndrome
Barth syndrome
Hereditary motor sensory neuropathy
Androgen insensitivity syndrome
Amelogenesis imperfecta
Adenosine deaminase deficiency
Dyskeratosis congenita
Hereditary disorder
Pachyonychia congenita
22q11.2 deletion syndrome
Hypophosphatasia
more...
See also
(20)
Nevus flammeus nuchae
Hyper IgM Syndrome Type 1
Anatomy
Integument
EDARADD
EDARADD
Genetic trait
Autosomal recessive
Autosomal dominant
Hypodontia
Simpson-Go- labi-Behmel syndrome
Birthmarks
Autosomal
Cadherin
Ectodermal
Hermann Werner Siemens
X-linked endothelial corneal dystrophy
KAL1
Immunodeficiency with hyper-IgM
Medicine
Karyotype
more...
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