MeSH D040181 - x-linked genetic diseases
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Competitive landscape
D030342:Inborn genetic diseases
D040181:
X-linked genetic diseases
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D000795:Fabry disease
D002836:Hemophilia b
D005489:Focal dermal hypoplasia
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D006015:Glycogen storage disease type viii
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D006105:Chronic granulomatous disease
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D009800:Oculocerebrorenal syndrome
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D013734:Androgen-insensitivity syndrome
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D014923:Wiskott-aldrich syndrome
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D015794:Choroideremia
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D016114:X-linked ichthyosis
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D019871:Dyskeratosis congenita
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D020371:Pelizaeus-merzbacher disease
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D020388:Duchenne muscular dystrophy
D020389:Emery-dreifuss muscular dystrophy
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D038901:X-linked mental retardation
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D052120:Glycogen storage disease type iib
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D053307:Type 1 hyper-igm immunodeficiency syndrome
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D053358:Anhidrotic ectodermal dysplasia 1
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D053632:X-linked combined immunodeficiency diseases
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D055534:X-linked bulbo-spinal atrophy
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D056830:Isolated noncompaction of the ventricular myocardium
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D056889:Barth syndrome
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D057973:Dent disease
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D058540:Aicardi syndrome
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Events Timeline
Commercial
No Data
Clinical Trials
Historical Success Rate
Phase 1
0%0/0
Phase 2
33%1/3
Phase 3
0%0/2
Approved: 0Overall Success rate: 0%
All Clinical Trials
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