Mesh term Genetic Diseases, X-Linked
Browse to parent terms:Genetic Diseases, Inborn
Description
Genetic diseases that are linked to gene mutations on the X CHROMOSOME in humans (X CHROMOSOME, HUMAN) or the X CHROMOSOME in other species. Included here are animal models of human X-linked diseases.Browse to child terms:
Aicardi Syndrome
Androgen-Insensitivity Syndrome
Barth Syndrome
Bulbo-Spinal Atrophy, X-Linked
Choroideremia
Dent Disease
Dyskeratosis Congenita
Ectodermal Dysplasia 1, Anhidrotic
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
Ichthyosis, X-Linked
Isolated Noncompaction of the Ventricular Myocardium
Mental Retardation, X-Linked
Muscular Dystrophy, Duchenne
Muscular Dystrophy, Emery-Dreifuss
Oculocerebrorenal Syndrome
Ornithine Carbamoyltransferase Deficiency Disease
Pelizaeus-Merzbacher Disease
Wiskott-Aldrich Syndrome
X-Linked Combined Immunodeficiency Diseases
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