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X-linked inheritance

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Information related to X-linked inheritance

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, Fragile X syndrome, IPEX syndrome, X-linked myotubular myopathy, Tranebjaerg–Svejgaard syndrome, Hyper-IgM syndrome type 1, Gustavson syndrome, Wu syndrome, Retinoschisis, Adrenoleukodystrophy, Wilson–Turner syndrome, X-linked endothelial corneal dystrophy, Spinal and bulbar muscular atrophy, Simpson–Golabi–Behmel syndrome, Smith–Fineman–Myers syndrome, TBX22

Sperm protein associated with the nucleus, X-linked, family member A1, Blue-cone monochromacy, DDX3X syndrome, Nonsyndromic deafness, PHF8, Conradi–Hünermann syndrome, Hypohidrotic ectodermal dysplasia, Congenital stationary night blindness, Allan–Herndon–Dudley syndrome, Snyder–Robinson syndrome, Genetic disorder, Sideroblastic anemia, Brunner syndrome, Muscular dystrophy, Neural tube defect, Charcot–Marie–Tooth disease, Aqueductal stenosis, Leigh syndrome, Object Linking and Embedding, Lesch–Nyhan syndrome, Situs ambiguus, Emery–Dreifuss muscular dystrophy, Familial exudative vitreoretinopathy, Hypogonadotropic hypogonadism, Satellaview, Situs inversus, Hypoparathyroidism, Nystagmus, Aortic arches, Hereditary spastic paraplegia, Spinocerebellar ataxia, Ectrodactyly, URL shortening, Senran Kagura, List of Super Robot Wars video games, Retinal dysplasia, Arthrogryposis, C0 and C1 control codes, Mitral valve prolapse, 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 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, Fragile X syndrome, IPEX syndrome, X-linked myotubular myopathy, Tranebjaerg–Svejgaard syndrome, Hyper-IgM syndrome type 1, Gustavson syndrome, Wu syndrome, Retinoschisis, Adrenoleukodystrophy, Wilson–Turner syndrome, X-linked endothelial corneal dystrophy, Spinal and bulbar muscular atrophy, Simpson–Golabi–Behmel syndrome, Smith–Fineman–Myers syndrome, TBX22, Sperm protein associated with the nucleus, X-linked, family member A1, Blue-cone monochromacy, DDX3X syndrome, Nonsyndromic deafness, PHF8, Conradi–Hünermann syndrome, Hypohidrotic ectodermal dysplasia, Congenital stationary night blindness, Allan–Herndon–Dudley syndrome, Snyder–Robinson syndrome, Genetic disorder, Sideroblastic anemia, Brunner syndrome, Muscular dystrophy, Neural tube defect, Charcot–Marie–Tooth disease, Aqueductal stenosis, Leigh syndrome, Object Linking and Embedding, Lesch–Nyhan syndrome, Situs ambiguus, Emery–Dreifuss muscular dystrophy, Familial exudative vitreoretinopathy, Hypogonadotropic hypogonadism, Satellaview, Situs inversus, Hypoparathyroidism, Nystagmus, Aortic arches, Hereditary spastic paraplegia, Spinocerebellar ataxia, Ectrodactyly, URL shortening, Senran Kagura, List of Super Robot Wars video games, Retinal dysplasia, Arthrogryposis, C0 and C1 control codes, Mitral valve prolapse, 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

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