X-linked gene

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, Tranebjaerg–Svejgaard syndrome, X-linked myotubular myopathy, Occipital horn syndrome, Fragile X syndrome, Hyper-IgM syndrome type 1, 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, Muscular dystrophy, Neural tube defect, Charcot–Marie–Tooth disease, Leigh syndrome, Aqueductal stenosis, Object Linking and Embedding, Lesch–Nyhan syndrome, Emery–Dreifuss muscular dystrophy, Situs ambiguus, Hypogonadotropic hypogonadism, Familial exudative vitreoretinopathy, Situs inversus, Satellaview, Nystagmus, Hypoparathyroidism, XMODEM, Spinocerebellar ataxia, Hereditary spastic paraplegia, Aortic arches, 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, Tranebjaerg–Svejgaard syndrome, X-linked myotubular myopathy, Occipital horn syndrome, Fragile X syndrome, Hyper-IgM syndrome type 1, 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, Muscular dystrophy, Neural tube defect, Charcot–Marie–Tooth disease, Leigh syndrome, Aqueductal stenosis, Object Linking and Embedding, Lesch–Nyhan syndrome, Emery–Dreifuss muscular dystrophy, Situs ambiguus, Hypogonadotropic hypogonadism, Familial exudative vitreoretinopathy, Situs inversus, Satellaview, Nystagmus, Hypoparathyroidism, XMODEM, Spinocerebellar ataxia, Hereditary spastic paraplegia, Aortic arches, 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, Andreas, Операція_«Антропоїд», حاجي_علي_بيك_(رباطات), Santa_Ynez_Valley_Union_High_School, Tentara_Pelajar, Hermanus, حفل_توزيع_جوائز_الأوسكار_السابع_والثمانون, Beast_(Chipmunk_song), واش_واتر_(باركشير), Daftar_stasiun_radio_di_Nusa_Tenggara_Timur, Amanda_Wyss, VisualEditor, King's_College_School, Жемчуг_дракона, Đại_học_Simon_Fraser, Loka,_Rumbia,_Jeneponto, Promozione_Trentino-Alto_Adige_1984-1985, Blekok_sawah, 1897_Auburn_Tigers_football_team, Olaf_III_of_Norway, Mario_Röser, Thư_viện_Công_cộng_New_York, Annabelle_Wallis, Palau_de_les_Arts_Reina_Sofía, Sint-Jansplein_(Antwerpen), Carola_Häggkvist, Biagio_Rossetti, Saltos_del_patinaje_artístico_sobre_hielo, Divorce_Act_(Canada), Международное_энергетическое_агентство, Meja, Юзеф_Ігнацій_Крашевський, 2018_Rally_Sweden, 上田祐司, Companiganj_Upazila,_Noakhali, Secretaría_de_Gobernación_(México), Asesinato_de_Samuel_Paty, المتحف_الوطني_للعلوم_الناشئة_والابتكار, معركة_فورت_واجنر_الثانية, Luvah, Юр'ївка_(Чернігівський_район), Rickling, Ayy_Ladies, Tom_Waring, Карраскаль-де-Баррегас, RT_America, İspanya_Millî_Kütüphanesi, Benteng_Revengie, كابل_ماوار_(أنغلزي), BBC_Philharmonic, Орловка_(Кыштовский_район), Derek_Luke, G.NA, Ekspedisi_Sulawesi_Selatan, Вулиця_Степана_Чобану_(Київ), Голландська_колонізація_Америки, Hibrida_siprinidae, Museum_Taman_Prasasti, PARC_(company), 著作権法_(アメリカ合衆国)