X-linked recessiveRedirect to: Information related to X-linked recessiveSex linkage, X-linked dominant inheritance, X-linked intellectual disability, X-linked recessive inheritance, X-linked thrombocytopenia, X-linked hypertrichosis, X-linked hypophosphatemia, X-linked agammaglobulinemia, X-linked ichthyosis, X-linked severe combined immunodeficiency, X-linked adrenal hypoplasia congenita, X-linked dystonia parkinsonism, X-linked complicated corpus callosum dysgenesis, Myopathy, X-linked, with excessive autophagy, ATR-X syndrome, X-linked Charcot–Marie–Tooth disease, X-linked spinal muscular atrophy type 2, X-linked reticulate pigmentary disorder, X-linked lymphoproliferative disease, X-linked recessive chondrodysplasia punctata, X-linked recessive hypoparathyroidism, VCX, X-linked sideroblastic anemia and spinocerebellar ataxia, X-linked cone-rod dystrophy, type 1, Link domain, Lujan–Fryns syndrome, IPEX syndrome, Tranebjaerg–Svejgaard syndrome, X-linked myotubular myopathy, Occipital horn syndrome, Hyper-IgM syndrome type 1, Fragile X syndrome, Gustavson syndrome, Wu syndrome, Adrenoleukodystrophy, Retinoschisis, Wilson–Turner syndrome, X-linked endothelial corneal dystrophy, Spinal and bulbar muscular atrophy, HNRNPH2-related disorders, Simpson–Golabi–Behmel syndrome Smith–Fineman–Myers syndrome, TBX22, Blue-cone monochromacy, Sperm protein associated with the nucleus, X-linked, family member A1, DDX3X syndrome, Nonsyndromic deafness, PHF8, Conradi–Hünermann syndrome, Hypohidrotic ectodermal dysplasia, Congenital stationary night blindness, Allan–Herndon–Dudley syndrome, Genetic disorder, Snyder–Robinson syndrome, Sideroblastic anemia, Neural tube defect, Muscular dystrophy, Brunner syndrome, Charcot–Marie–Tooth disease, Aqueductal stenosis, Leigh syndrome, Object Linking and Embedding, Lesch–Nyhan syndrome, Situs ambiguus, Emery–Dreifuss muscular dystrophy, Familial exudative vitreoretinopathy, Hypogonadotropic hypogonadism, Situs inversus, Satellaview, Nystagmus, Hypoparathyroidism, XMODEM, Spinocerebellar ataxia, Hereditary spastic paraplegia, Aortic arches, Ectrodactyly, URL shortening, Senran Kagura, Mitral valve prolapse, Arthrogryposis, List of Super Robot Wars video games, Neutropenia, Retinal dysplasia, C0 and C1 control codes, Telegram (software), Heart valve dysplasia, Dwarfism, Tetra-amelia syndrome, Hair loss, Internet in South Africa, VMware ThinApp Sex linkage, X-linked dominant inheritance, X-linked intellectual disability, X-linked recessive inheritance, X-linked thrombocytopenia, X-linked hypertrichosis, X-linked hypophosphatemia, X-linked agammaglobulinemia, X-linked ichthyosis, X-linked severe combined immunodeficiency, X-linked adrenal hypoplasia congenita, X-linked dystonia parkinsonism, X-linked complicated corpus callosum dysgenesis, Myopathy, X-linked, with excessive autophagy, ATR-X syndrome, X-linked Charcot–Marie–Tooth disease, X-linked spinal muscular atrophy type 2, X-linked reticulate pigmentary disorder, X-linked lymphoproliferative disease, X-linked recessive chondrodysplasia punctata, X-linked recessive hypoparathyroidism, VCX, X-linked sideroblastic anemia and spinocerebellar ataxia, X-linked cone-rod dystrophy, type 1, Link domain, Lujan–Fryns syndrome, IPEX syndrome, Tranebjaerg–Svejgaard syndrome, X-linked myotubular myopathy, Occipital horn syndrome, Hyper-IgM syndrome type 1, Fragile X syndrome, Gustavson syndrome, Wu syndrome, Adrenoleukodystrophy, Retinoschisis, Wilson–Turner syndrome, X-linked endothelial corneal dystrophy, Spinal and bulbar muscular atrophy, HNRNPH2-related disorders, Simpson–Golabi–Behmel syndrome, Smith–Fineman–Myers syndrome, TBX22, Blue-cone monochromacy, Sperm protein associated with the nucleus, X-linked, family member A1, DDX3X syndrome, Nonsyndromic deafness, PHF8, Conradi–Hünermann syndrome, Hypohidrotic ectodermal dysplasia, Congenital stationary night blindness, Allan–Herndon–Dudley syndrome, Genetic disorder, Snyder–Robinson syndrome, Sideroblastic anemia, Neural tube defect, Muscular dystrophy, Brunner syndrome, Charcot–Marie–Tooth disease, Aqueductal stenosis, Leigh syndrome, Object Linking and Embedding, Lesch–Nyhan syndrome, Situs ambiguus, Emery–Dreifuss muscular dystrophy, Familial exudative vitreoretinopathy, Hypogonadotropic hypogonadism, Situs inversus, Satellaview, Nystagmus, Hypoparathyroidism, XMODEM, Spinocerebellar ataxia, Hereditary spastic paraplegia, Aortic arches, Ectrodactyly, URL shortening, Senran Kagura, Mitral valve prolapse, Arthrogryposis, List of Super Robot Wars video games, Neutropenia, Retinal dysplasia, C0 and C1 control codes, Telegram (software), Heart valve dysplasia, Dwarfism, Tetra-amelia syndrome, Hair loss, Internet in South Africa, VMware ThinApp, Ravinder_Singh_(wrestler), Яфаново_(Ивановская_область), رونالدو_(فيلم), Bremen-Verden_campaign, Gempa_bumi_dan_tsunami_Sulawesi_2018, Hambre_(novela), دوري_كرة_السلة_التشيكي_للسيدات, Wolf_(phim_truyền_hình_Thái_Lan), Haiptling, 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