X-linked dominantRedirect to: Information related to X-linked dominantSex 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 lymphoproliferative disease, X-linked reticulate pigmentary disorder, 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, Retinoschisis, Wilson–Turner syndrome, X-linked endothelial corneal dystrophy, HNRNPH2-related disorders, Spinal and bulbar muscular atrophy, Simpson–Golabi–Behmel syndrome Smith–Fineman–Myers syndrome, TBX22, DDX3X syndrome, Sperm protein associated with the nucleus, X-linked, family member A1, Blue-cone monochromacy, PHF8, Nonsyndromic deafness, Conradi–Hünermann syndrome, Hypohidrotic ectodermal dysplasia, Congenital stationary night blindness, Allan–Herndon–Dudley syndrome, Genetic disorder, Snyder–Robinson syndrome, Sideroblastic anemia, Brunner syndrome, Muscular dystrophy, Neural tube defect, Charcot–Marie–Tooth disease, Aqueductal stenosis, Leigh syndrome, Object Linking and Embedding, Lesch–Nyhan syndrome, Emery–Dreifuss muscular dystrophy, Situs ambiguus, Familial exudative vitreoretinopathy, Hypogonadotropic hypogonadism, Situs inversus, Satellaview, Nystagmus, Hypoparathyroidism, XMODEM, Spinocerebellar ataxia, Aortic arches, Hereditary spastic paraplegia, Ectrodactyly, URL shortening, Senran Kagura, Mitral valve prolapse, List of Super Robot Wars video games, Retinal dysplasia, Arthrogryposis, Neutropenia, 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 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 lymphoproliferative disease, X-linked reticulate pigmentary disorder, 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, Retinoschisis, Wilson–Turner syndrome, X-linked endothelial corneal dystrophy, HNRNPH2-related disorders, Spinal and bulbar muscular atrophy, Simpson–Golabi–Behmel syndrome, Smith–Fineman–Myers syndrome, TBX22, DDX3X syndrome, Sperm protein associated with the nucleus, X-linked, family member A1, Blue-cone monochromacy, PHF8, Nonsyndromic deafness, Conradi–Hünermann syndrome, Hypohidrotic ectodermal dysplasia, Congenital stationary night blindness, Allan–Herndon–Dudley syndrome, Genetic disorder, Snyder–Robinson syndrome, Sideroblastic anemia, Brunner syndrome, Muscular dystrophy, Neural tube defect, Charcot–Marie–Tooth disease, Aqueductal stenosis, Leigh syndrome, Object Linking and Embedding, Lesch–Nyhan syndrome, Emery–Dreifuss muscular dystrophy, Situs ambiguus, Familial exudative vitreoretinopathy, Hypogonadotropic hypogonadism, Situs inversus, Satellaview, Nystagmus, Hypoparathyroidism, XMODEM, Spinocerebellar ataxia, Aortic arches, Hereditary spastic paraplegia, Ectrodactyly, URL shortening, Senran Kagura, Mitral valve prolapse, List of Super Robot Wars video games, Retinal dysplasia, Arthrogryposis, Neutropenia, C0 and C1 control codes, Telegram (software), Heart valve dysplasia, Dwarfism, Tetra-amelia syndrome, Hair loss, Internet in South Africa, VMware ThinApp, Tourisme_en_Espagne, Crack-Up_(1946_film), Oostenrijkse_hockeyploeg_(mannen), Порядок_наследования_мексиканского_престола, RX_J1347.5−1145, جامع_فاطمة_الزهراء_(الأنبار), Сюда_идёт_кот!_(мультфильм), Rambahadur_Limbu, 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Даріо_Бенедетто, The_Autumn_Ballad, راسم_أحادي, Oberon_Dam, Christopher_Newport, Michael_Smith_(chemist), 7-ма_армія_(Третій_Рейх), Voice_of_an_Angel, TF1_Séries_Films, Cúp_bóng_đá_1000_năm_Thăng_Long_–_Hà_Nội_(khu_vực_Hà_Nội), Concepción_Heredia_y_Grund, Ante_Čović, Pengeboman_Abuja_April_2014, I'll_Take_the_Rain, Ma_Cao_thuộc_Bồ_Đào_Nha |
