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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, Lujan–Fryns syndrome, Fragile X syndrome, IPEX syndrome, Tranebjaerg–Svejgaard syndrome, X-linked myotubular myopathy, Hyper-IgM syndrome type 1, Gustavson syndrome, Wu syndrome, Retinoschisis, Adrenoleukodystrophy, Wilson–Turner syndrome, Spinal and bulbar muscular atrophy, X-linked endothelial corneal dystrophy, 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, Conradi–Hünermann syndrome, PHF8, Hypohidrotic ectodermal dysplasia, Congenital stationary night blindness, Allan–Herndon–Dudley syndrome, Genetic disorder, Snyder–Robinson syndrome, Sideroblastic anemia, Neural tube defect, Charcot–Marie–Tooth disease, Muscular dystrophy, Brunner syndrome, Leigh syndrome, Aqueductal stenosis, Object Linking and Embedding, Lesch–Nyhan syndrome, Emery–Dreifuss muscular dystrophy, Situs ambiguus, Hypogonadotropic hypogonadism, Familial exudative vitreoretinopathy, Satellaview, Situs inversus, Nystagmus, Hypoparathyroidism, Hereditary spastic paraplegia, Aortic arches, Spinocerebellar ataxia, Ectrodactyly, URL shortening, Senran Kagura, Arthrogryposis, List of Super Robot Wars video games, Mitral valve prolapse, Retinal dysplasia, C0 and C1 control codes, Telegram (software), Neutropenia, 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)
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, Lujan–Fryns syndrome, Fragile X syndrome, IPEX syndrome, Tranebjaerg–Svejgaard syndrome, X-linked myotubular myopathy, Hyper-IgM syndrome type 1, Gustavson syndrome, Wu syndrome, Retinoschisis, Adrenoleukodystrophy, Wilson–Turner syndrome, Spinal and bulbar muscular atrophy, X-linked endothelial corneal dystrophy, 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, Conradi–Hünermann syndrome, PHF8, Hypohidrotic ectodermal dysplasia, Congenital stationary night blindness, Allan–Herndon–Dudley syndrome, Genetic disorder, Snyder–Robinson syndrome, Sideroblastic anemia, Neural tube defect, Charcot–Marie–Tooth disease, Muscular dystrophy, Brunner syndrome, Leigh syndrome, Aqueductal stenosis, Object Linking and Embedding, Lesch–Nyhan syndrome, Emery–Dreifuss muscular dystrophy, Situs ambiguus, Hypogonadotropic hypogonadism, Familial exudative vitreoretinopathy, Satellaview, Situs inversus, Nystagmus, Hypoparathyroidism, Hereditary spastic paraplegia, Aortic arches, Spinocerebellar ataxia, Ectrodactyly, URL shortening, Senran Kagura, Arthrogryposis, List of Super Robot Wars video games, Mitral valve prolapse, Retinal dysplasia, C0 and C1 control codes, Telegram (software), Neutropenia, 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, Lembaga_Pemasyarakatan_Sarolangun, Pierre_Schoendoerffer, Korps_Samapta_Bhayangkara_Baharkam_Polri, هندسة_نانوية, Южный_вокзал_(станция_метро,_Харьков), 6-й_гвардейский_кавалерийский_корпус, Vita_huset, Ульдіс_Аугуліс, Slipstream_(2005_film), Airspeed_Ltd., Terry_Becker, Harold_Teen, Norwegian_Wood_(novel), Kinahan_Organised_Crime_Group, Agente_consolare, Hanoi_Radio_Television, Yehezkiel_42, Астон_Вилла, Leonard_W._Schuetz, Краснопавловка_(Харьковская_область), سرديان_سافيتش, Romanian_prisoners_of_war_in_the_Soviet_Union, Shot_transition_detection, Пиджак, Hougomont_(barque), Kusuriya_no_Hitorigoto, Infantry_in_the_American_Civil_War, Puteri_Indonesia_Sulawesi_Selatan, Pemilihan_umum_Bupati_Kampar_2024, F.C._Sassari_Torres_Femminile, John_O'Donohoe, The_Voice_Kids_(British_TV_series), John_Rolle_(died_1706), Vampire_Hunter_D:_Mysterious_Journey_to_the_North_Sea, 45-я_бомбардировочная_авиационная_дивизия, Хоккей_с_шайбой_на_зимних_Олимпийских_играх_1972, Daftar_Wakil_Bupati_Nias_Utara, 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, Пулитцеровская_премия_за_художественную_книгу, 中国中央电视台相关争议, Philippe_Saurel