Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Genetic Diseases, X-Linked
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. MeSH
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Subtype Terms (25)
Aicardi Syndrome
5 approved drugs
Androgen-Insensitivity Syndrome
Barth Syndrome
2 drugs (1 approved, 1 experimental)
Bulbo-Spinal Atrophy, X-Linked
5 drugs (4 approved, 1 experimental)
Choroideremia
7 drugs (2 approved, 5 experimental)
Dent Disease
2 approved drugs
Dyskeratosis Congenita
12 drugs (11 approved, 1 experimental)
Ectodermal Dysplasia 1, Anhidrotic
2 drugs (1 approved, 1 experimental)
Fabry Disease
20 drugs (10 approved, 10 experimental)
Glycogen Storage Disease Type IIb
1 experimental drug
Glycogen Storage Disease Type VIII
Granulomatous Disease, Chronic
39 drugs (26 approved, 13 experimental)
Hemophilia B
43 drugs (14 approved, 29 experimental)
Hyper-IgM Immunodeficiency Syndrome, Type 1
9 approved drugs
Isolated Noncompaction of the Ventricular Myocardium
Mental Retardation, X-Linked
1 approved drug
Muscular Dystrophy, Duchenne
91 drugs (38 approved, 53 experimental)
Muscular Dystrophy, Emery-Dreifuss
Ornithine Carbamoyltransferase Deficiency Disease
7 drugs (1 approved, 6 experimental)
Pelizaeus-Merzbacher Disease
3 drugs (1 approved, 2 experimental)
Wiskott-Aldrich Syndrome
35 drugs (25 approved, 10 experimental)
X-Linked Combined Immunodeficiency Diseases
19 drugs (10 approved, 9 experimental)
Phase 3 Indicated Drugs (4)
Phase 1 Indicated Drugs (1)
Other Experimental Indicated Drugs (1)
Organization Involved with Phase 3 Indications (4)
Organization Involved with Phase 2 Indications (15)
Organization Involved with Other Experimental Indications (2)
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UMLS Data
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