X-linked recessive

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, Tranebjaerg–Svejgaard syndrome, X-linked myotubular myopathy, 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

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, Snyder–Robinson syndrome, Genetic disorder, Sideroblastic anemia, Brunner syndrome, Neural tube defect, Muscular dystrophy, 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, 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, Retinal dysplasia, Telegram (software), Mitral valve prolapse, C0 and C1 control codes, Heart valve dysplasia, Neutropenia, Dwarfism, Tetra-amelia syndrome, Hair loss, Internet in South Africa, VMware ThinApp, Template_talk:Military_ranks, Політика_США, Himalaya_Energi_Perkasa

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, Tranebjaerg–Svejgaard syndrome, X-linked myotubular myopathy, 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, 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, Snyder–Robinson syndrome, Genetic disorder, Sideroblastic anemia, Brunner syndrome, Neural tube defect, Muscular dystrophy, 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, 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, Retinal dysplasia, Telegram (software), Mitral valve prolapse, C0 and C1 control codes, Heart valve dysplasia, Neutropenia, Dwarfism, Tetra-amelia syndrome, Hair loss, Internet in South Africa, VMware ThinApp, Template_talk:Military_ranks, Політика_США, Himalaya_Energi_Perkasa, Biblioteca_Joanina, Party_Down_South, Intervensi_Belanda_di_Bali_(1858), Left_and_Leaving, آصف_علي_مالك, بوابة:آل_سعود, دليل_إندونيسيا, Dedham_Public_Library, Golf_in_the_United_States, Single-artist_museum, Sejarah_Kota_Banjarmasin, Kirati_people, Tata_Bahasa_Baku_Bahasa_Indonesia, Historia_de_Nigeria, Prime_Minister_of_Sweden, لابانو, Phoenix_(banda), Rheinland, Lijst_van_kranten_in_België, Incentives_for_Olympic_medalists_by_country, Laos, Arthur_Bisguier, Julia_Capulet, حكومة_حمادي_الجبالي, 53rd_Berlin_International_Film_Festival, Stiffelio, Line_15_(São_Paulo_Metro), List_of_Syrian_television_series, Muhammad_Kamil, La_Sociedad, جمال_(مدينة), Diocesi_di_Termoli-Larino, Shlomo_Kalish, ThinkPad, Comunità_collinare, Marjorie_Strider, مناخة_(صنعاء), 1796_United_States_House_of_Representatives_elections_in_South_Carolina, أليكس_ديلا_فالي, ماساهيرو_أكيموتو_(متزلج_قفز), Athletics_at_the_2006_Commonwealth_Games_–_Women's_discus_throw, العلاقات_الليتوانية_المصرية, Revolução_de_1946_no_Haiti, Главні_надражі_(станція_метро), Kungliga_slott_i_Sverige, 川崎医療短期大学, WTKT, 1992_Boise_State_Broncos_football_team, Huffman_coding, Горизонтальне_оперення, Rage_of_Bahamut_(TV_series), Moyen-Orient, List_of_Orders_in_Council_for_Northern_Ireland, Broad_Bay,_New_Zealand, Atalaia_(arquitetura), كأس_ديفيز_1980, FedEx_Express_Flight_1406, Sekar_Mayang, Reseptor_(biokimia), Tepēyōllōtl