X-linked inheritanceRedirect to: Information related to X-linked inheritanceSex 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 severe combined immunodeficiency, X-linked ichthyosis, 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, Occipital horn syndrome, Tranebjaerg–Svejgaard syndrome, X-linked myotubular myopathy, Hyper-IgM syndrome type 1, Fragile X syndrome, Gustavson syndrome, Wu syndrome, Adrenoleukodystrophy, Wilson–Turner syndrome, Retinoschisis, Spinal and bulbar muscular atrophy, X-linked endothelial corneal dystrophy, 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, Congenital stationary night blindness, Hypohidrotic ectodermal dysplasia, Allan–Herndon–Dudley syndrome, Genetic disorder, Snyder–Robinson syndrome, Sideroblastic anemia, Neural tube defect, Brunner syndrome, 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, Nystagmus, Situs inversus, Satellaview, Hypoparathyroidism, XMODEM, Spinocerebellar ataxia, Aortic arches, Hereditary spastic paraplegia, Ectrodactyly, URL shortening, Senran Kagura, Mitral valve prolapse, Arthrogryposis, List of Super Robot Wars video games, Retinal dysplasia, Neutropenia, 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 recessive inheritance, X-linked thrombocytopenia, X-linked hypertrichosis, X-linked hypophosphatemia, X-linked agammaglobulinemia, X-linked severe combined immunodeficiency, X-linked ichthyosis, 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, Occipital horn syndrome, Tranebjaerg–Svejgaard syndrome, X-linked myotubular myopathy, Hyper-IgM syndrome type 1, Fragile X syndrome, Gustavson syndrome, Wu syndrome, Adrenoleukodystrophy, Wilson–Turner syndrome, Retinoschisis, Spinal and bulbar muscular atrophy, X-linked endothelial corneal dystrophy, 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, Congenital stationary night blindness, Hypohidrotic ectodermal dysplasia, Allan–Herndon–Dudley syndrome, Genetic disorder, Snyder–Robinson syndrome, Sideroblastic anemia, Neural tube defect, Brunner syndrome, 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, Nystagmus, Situs inversus, Satellaview, Hypoparathyroidism, XMODEM, Spinocerebellar ataxia, Aortic arches, Hereditary spastic paraplegia, Ectrodactyly, URL shortening, Senran Kagura, Mitral valve prolapse, Arthrogryposis, List of Super Robot Wars video games, Retinal dysplasia, Neutropenia, Telegram (software), C0 and C1 control codes, Heart valve dysplasia, Dwarfism, Tetra-amelia syndrome, Hair loss, Internet in South Africa, VMware ThinApp, Clásica_de_San_Sebastián_1987, Taman_Sari,_Jakarta_Barat, James_Prigoff, Lijst_van_oorlogen_van_Nederland, Gunung_Pengsong, リラヴァティ_(競走馬), The_Plank_(1967_film), دوري_الدرجة_الأولى_الأرجنتيني_2015, Israëlische_landmacht, 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