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Congenital Disorder

Genetic Diseases, X-Linked

AMW:DIS:160059

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.

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Genetic Diseases, X-Linked has parent Genetic Diseases, Inborn
Focal Dermal Hypoplasia has parent Genetic Diseases, X-Linked
Muscular Dystrophy, Duchenne has parent Genetic Diseases, X-Linked
Muscular Dystrophy, Emery-Dreifuss has parent Genetic Diseases, X-Linked
Pelizaeus-Merzbacher Disease has parent Genetic Diseases, X-Linked
Fabry Disease has parent Genetic Diseases, X-Linked
Oculocerebrorenal Syndrome has parent Genetic Diseases, X-Linked
Ornithine Carbamoyltransferase Deficiency Disease has parent Genetic Diseases, X-Linked
Bulbo-Spinal Atrophy, X-Linked has parent Genetic Diseases, X-Linked
Aicardi Syndrome has parent Genetic Diseases, X-Linked
X-Linked Intellectual Disability has parent Genetic Diseases, X-Linked
Glycogen Storage Disease Type IIb has parent Genetic Diseases, X-Linked
Choroideremia has parent Genetic Diseases, X-Linked
Androgen-Insensitivity Syndrome has parent Genetic Diseases, X-Linked
Dent Disease has parent Genetic Diseases, X-Linked
Barth Syndrome has parent Genetic Diseases, X-Linked
Isolated Noncompaction of the Ventricular Myocardium has parent Genetic Diseases, X-Linked
Hemophilia B has parent Genetic Diseases, X-Linked
Wiskott-Aldrich Syndrome has parent Genetic Diseases, X-Linked
Hyper-IgM Immunodeficiency Syndrome, Type 1 has parent Genetic Diseases, X-Linked
Dyskeratosis Congenita has parent Genetic Diseases, X-Linked
Granulomatous Disease, Chronic has parent Genetic Diseases, X-Linked
Ectodermal Dysplasia 1, Anhidrotic has parent Genetic Diseases, X-Linked
Ichthyosis, X-Linked has parent Genetic Diseases, X-Linked
Glycogen Storage Disease Type VIII has parent Genetic Diseases, X-Linked
X-Linked Combined Immunodeficiency Diseases has parent Genetic Diseases, X-Linked

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