X-linked recessiveRedirect to: Information related to X-linked recessiveSex linkage, X-linked dominant inheritance, X-linked intellectual disability, X-linked thrombocytopenia, X-linked recessive inheritance, 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, IPEX syndrome, Lujan–Fryns syndrome, Occipital horn syndrome, Tranebjaerg–Svejgaard syndrome, X-linked myotubular myopathy, 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, DDX3X syndrome, Sperm protein associated with the nucleus, X-linked, family member A1, Nonsyndromic deafness, Conradi–Hünermann syndrome, PHF8, Hypohidrotic ectodermal dysplasia, Congenital stationary night blindness, Allan–Herndon–Dudley syndrome, Genetic disorder, Snyder–Robinson syndrome, Sideroblastic anemia, Brunner syndrome, Neural tube defect, Muscular dystrophy, Charcot–Marie–Tooth disease, Aqueductal stenosis, Leigh syndrome, Object Linking and Embedding, Lesch–Nyhan syndrome, Emery–Dreifuss muscular dystrophy, Situs ambiguus, Hypogonadotropic hypogonadism, Familial exudative vitreoretinopathy, Situs inversus, Satellaview, Nystagmus, Hypoparathyroidism, XMODEM, Hereditary spastic paraplegia, Aortic arches, Spinocerebellar ataxia, Ectrodactyly, URL shortening, Mitral valve prolapse, Senran Kagura, Arthrogryposis, List of Super Robot Wars video games, Neutropenia, Retinal dysplasia, Telegram (software), C0 and C1 control codes, 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 thrombocytopenia, X-linked recessive inheritance, 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, IPEX syndrome, Lujan–Fryns syndrome, Occipital horn syndrome, Tranebjaerg–Svejgaard syndrome, X-linked myotubular myopathy, 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, DDX3X syndrome, Sperm protein associated with the nucleus, X-linked, family member A1, Nonsyndromic deafness, Conradi–Hünermann syndrome, PHF8, Hypohidrotic ectodermal dysplasia, Congenital stationary night blindness, Allan–Herndon–Dudley syndrome, Genetic disorder, Snyder–Robinson syndrome, Sideroblastic anemia, Brunner syndrome, Neural tube defect, Muscular dystrophy, Charcot–Marie–Tooth disease, Aqueductal stenosis, Leigh syndrome, Object Linking and Embedding, Lesch–Nyhan syndrome, Emery–Dreifuss muscular dystrophy, Situs ambiguus, Hypogonadotropic hypogonadism, Familial exudative vitreoretinopathy, Situs inversus, Satellaview, Nystagmus, Hypoparathyroidism, XMODEM, Hereditary spastic paraplegia, Aortic arches, Spinocerebellar ataxia, Ectrodactyly, URL shortening, Mitral valve prolapse, Senran Kagura, Arthrogryposis, List of Super Robot Wars video games, Neutropenia, Retinal dysplasia, Telegram (software), C0 and C1 control codes, Heart valve dysplasia, Dwarfism, Tetra-amelia syndrome, Hair loss, Internet in South Africa, VMware ThinApp, Шумське, Dewan_Perwakilan_Rakyat_Daerah_Kabupaten_Ciamis, Tjahaja_Pasoendan, Irish_cricket_team_in_the_West_Indies_in_2021–22, Weathering_with_You, Christian_Lundeberg, Park_Si-hoo, CCTV-9, Fossalta_di_Piave, Hiro_Pembela_Bumi, 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