KnowraX-linked inheritanceLinked fromLinked fromThe 21 pages that link to X-linked inheritance, each with the reason it gives.All 21Broader topic 2Related 13Narrower topic 4Compared with 2Color blindnessRelated: Common red–green deficiencies are often X-linked, making them more frequent in males.Retinitis pigmentosaRelated: X-linked forms often cause severe disease in males and follow distinct family patterns.X chromosomeRelated: Its inheritance differs between people with one X chromosome and those with two.Carrier screeningRelated: Some screened variants can cause conditions through X-linked inheritance rather than recessive inheritance.Genetic disorderRelated: X-linked disorders often show different inheritance patterns in people with one or two X chromosomes.Alport syndromeRelated: Most classic Alport syndrome is X-linked and caused by COL4A5 variants.Chronic granulomatous diseaseRelated: Most cases arise from variants in the X-linked CYBB gene.Charcot–Marie–Tooth diseaseRelated: The common CMT1X form follows this pattern and can affect sexes differently.DichromacyRelated: Common red–green dichromacy often follows X-linked inheritance of cone-opsin gene changes.Becker muscular dystrophyRelated: DMD variants are X-linked, shaping who is affected and how variants pass through families.Kabuki syndromeRelated: KDM6A is X-linked, shaping how its Kabuki syndrome variant can be inherited and expressed.Pelizaeus–Merzbacher diseaseRelated: PLP1 lies on the X chromosome, so inheritance patterns vary between males and females.Aarskog–Scott syndromeRelated: FGD1 lies on the X chromosome, shaping how the syndrome is inherited.