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Genetic Diseases, X-Linked

AMW:DIS:160059

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Genetic Diseases, InbornCongenital Disorder

Focus nodeGenetic Diseases, X-LinkedAMW:DIS:160059

25 direct children

• Aicardi SyndromeSyndrome · 0 children Focus
• Androgen-Insensitivity SyndromeSyndrome · 0 children Focus
• Barth SyndromeSyndrome · 0 children Focus
• Bulbo-Spinal Atrophy, X-LinkedDegenerative Disorder · 0 children Focus
• ChoroideremiaCongenital Disorder · 0 children Focus
• Dent DiseaseCongenital Disorder · 0 children Focus
• Dyskeratosis CongenitaCongenital Disorder · 0 children Focus
• Ectodermal Dysplasia 1, AnhidroticPathologic Condition · 0 children Focus
• Fabry DiseaseCongenital Disorder · 0 children Focus
• Focal Dermal HypoplasiaCongenital Disorder · 0 children Focus
• Glycogen Storage Disease Type IIbCongenital Disorder · 0 children Focus
• Glycogen Storage Disease Type VIIICongenital Disorder · 0 children Focus
• Granulomatous Disease, ChronicCongenital Disorder · 0 children Focus
• Hemophilia BCongenital Disorder · 0 children Focus
• Hyper-IgM Immunodeficiency Syndrome, Type 1Syndrome · 0 children Focus
• Ichthyosis, X-LinkedCongenital Disorder · 0 children Focus
• Isolated Noncompaction of the Ventricular MyocardiumCongenital Disorder · 0 children Focus
• Muscular Dystrophy, DuchenneCongenital Disorder · 0 children Focus
Muscular Dystrophy, Emery-DreifussCongenital Disorder · 2 children Focus
• Oculocerebrorenal SyndromeSyndrome · 0 children Focus
• Ornithine Carbamoyltransferase Deficiency DiseaseCongenital Disorder · 0 children Focus
• Pelizaeus-Merzbacher DiseaseCongenital Disorder · 0 children Focus
• Wiskott-Aldrich SyndromeSyndrome · 0 children Focus
• X-Linked Combined Immunodeficiency DiseasesImmune Disorder · 0 children Focus
X-Linked Intellectual DisabilityCongenital Disorder · 10 children Focus