ONKI3 | Medical Subject Headings

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Ectodermal Dysplasia 1, Anhidrotic

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Abnormalities, Multiple ∟ Ectodermal Dysplasia ∟ Ectodermal Dysplasia 1, Anhidrotic 24 coordinate concepts ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Fabry Disease \| ∟ Focal Dermal Hypoplasia \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hemophilia B \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Mental Retardation, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ Wiskott-Aldrich Syndrome \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Ectodermal Dysplasia 3, Anhidrotic \| ∟ Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive \| ∟ Ellis-Van Creveld Syndrome \| ∟ Neurocutaneous Syndromes \| ∟ Pachyonychia Congenita Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Skin Abnormalities ∟ Ectodermal Dysplasia ∟ Ectodermal Dysplasia 1, Anhidrotic 24 coordinate concepts ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Fabry Disease \| ∟ Focal Dermal Hypoplasia \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hemophilia B \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Mental Retardation, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ Wiskott-Aldrich Syndrome \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Ectodermal Dysplasia 3, Anhidrotic \| ∟ Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive \| ∟ Ellis-Van Creveld Syndrome \| ∟ Neurocutaneous Syndromes \| ∟ Pachyonychia Congenita Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Genetic Diseases, X-Linked ∟ Ectodermal Dysplasia 1, Anhidrotic 24 coordinate concepts ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Fabry Disease \| ∟ Focal Dermal Hypoplasia \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hemophilia B \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Mental Retardation, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ Wiskott-Aldrich Syndrome \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Ectodermal Dysplasia 3, Anhidrotic \| ∟ Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive \| ∟ Ellis-Van Creveld Syndrome \| ∟ Neurocutaneous Syndromes \| ∟ Pachyonychia Congenita Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Ectodermal Dysplasia ∟ Ectodermal Dysplasia 1, Anhidrotic 24 coordinate concepts ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Fabry Disease \| ∟ Focal Dermal Hypoplasia \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hemophilia B \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Mental Retardation, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ Wiskott-Aldrich Syndrome \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Ectodermal Dysplasia 3, Anhidrotic \| ∟ Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive \| ∟ Ellis-Van Creveld Syndrome \| ∟ Neurocutaneous Syndromes \| ∟ Pachyonychia Congenita Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Abnormalities ∟ Ectodermal Dysplasia ∟ Ectodermal Dysplasia 1, Anhidrotic 24 coordinate concepts ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Fabry Disease \| ∟ Focal Dermal Hypoplasia \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hemophilia B \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Mental Retardation, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ Wiskott-Aldrich Syndrome \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Ectodermal Dysplasia 3, Anhidrotic \| ∟ Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive \| ∟ Ellis-Van Creveld Syndrome \| ∟ Neurocutaneous Syndromes \| ∟ Pachyonychia Congenita Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Ectodermal Dysplasia ∟ Ectodermal Dysplasia 1, Anhidrotic 24 coordinate concepts ∟ Androgen-Insensitivity Syndrome \| ∟ Choroideremia \| ∟ Dyskeratosis Congenita \| ∟ Fabry Disease \| ∟ Focal Dermal Hypoplasia \| ∟ Glycogen Storage Disease Type IIb \| ∟ Glycogen Storage Disease Type VIII \| ∟ Granulomatous Disease, Chronic \| ∟ Hemophilia B \| ∟ Hyper-IgM Immunodeficiency Syndrome, Type 1 \| ∟ Hypophosphatemic Rickets, X-Linked Dominant \| ∟ Ichthyosis, X-Linked \| ∟ Mental Retardation, X-Linked \| ∟ Muscular Dystrophy, Duchenne \| ∟ Muscular Dystrophy, Emery-Dreifuss \| ∟ Oculocerebrorenal Syndrome \| ∟ Pelizaeus-Merzbacher Disease \| ∟ Wiskott-Aldrich Syndrome \| ∟ X-Linked Combined Immunodeficiency Diseases \| ∟ Ectodermal Dysplasia 3, Anhidrotic \| ∟ Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive \| ∟ Ellis-Van Creveld Syndrome \| ∟ Neurocutaneous Syndromes \| ∟ Pachyonychia Congenita X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Abnormalities, Multiple ∟ Ectodermal Dysplasia ∟ Ectodermal Dysplasia 1, Anhidrotic Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Skin Abnormalities ∟ Ectodermal Dysplasia ∟ Ectodermal Dysplasia 1, Anhidrotic Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Genetic Diseases, X-Linked ∟ Ectodermal Dysplasia 1, Anhidrotic Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Ectodermal Dysplasia ∟ Ectodermal Dysplasia 1, Anhidrotic Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Abnormalities ∟ Ectodermal Dysplasia ∟ Ectodermal Dysplasia 1, Anhidrotic Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Ectodermal Dysplasia ∟ Ectodermal Dysplasia 1, Anhidrotic Ectodermal Dysplasia > Abnormalities, Multiple > Abnormalities > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Ectodermal Dysplasia > Skin Abnormalities > Abnormalities > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Genetic Diseases, X-Linked > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Ectodermal Dysplasia > Skin Diseases, Genetic > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Ectodermal Dysplasia > Skin Abnormalities > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) Ectodermal Dysplasia > Skin Diseases, Genetic > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) X
historyNote*:	2007(1993) X
publicMeSHNote*:	2007; see ECTODERMAL DYSPLASIA 1993-2006 X
Scope note:	An X-linked form of ectodermal dysplasia which results from mutations of the gene encoding ECTODYSPLASIN. X
activeMeSHYear*:	2007X
dateCreated*:	2006-07-05X
dateEstablished*:	2007-01-01X
recordAuthorizer*:	sjnX
recordMaintainer*:	jmpX
recordOriginator*:	jmpX
Type:	Concept X
Coordinate terms:	Androgen-Insensitivity Syndrome \| Choroideremia \| Dyskeratosis Congenita \| Fabry Disease \| Focal Dermal Hypoplasia \| Glycogen Storage Disease Type IIb \| Glycogen Storage Disease Type VIII \| Granulomatous Disease, Chronic \| Hemophilia B \| Hyper-IgM Immunodeficiency Syndrome, Type 1 \| Hypophosphatemic Rickets, X-Linked Dominant \| Ichthyosis, X-Linked \| Mental Retardation, X-Linked \| Muscular Dystrophy, Duchenne \| Muscular Dystrophy, Emery-Dreifuss \| Oculocerebrorenal Syndrome \| Pelizaeus-Merzbacher Disease \| Wiskott-Aldrich Syndrome \| X-Linked Combined Immunodeficiency Diseases \| Ectodermal Dysplasia 3, Anhidrotic \| Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive \| Ellis-Van Creveld Syndrome \| Neurocutaneous Syndromes \| Pachyonychia Congenita X
URI:	X
Labels and equivalent concepts:	Anhidroottinen ektodermaalinen dysplasia 1 (fi) Ectodermal Dysplasia, Hypohydridic, X-Linked (en, replaced) X-Linked Hypohydridrotic Ectodermal Dysplasia (en, replaced) Ectodermal Dysplasia 1, Anhydrotic (en, replaced) Christ-Siemens-Touraine Syndrome (en, replaced) Anhydrotic Ectodermal Dysplasia, X-Linked (en, replaced) Anhidrotic Ectodermal Dysplasia, X-Linked (en, replaced) X
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