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 severe combined immunodeficiency, X-linked ichthyosis, 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, Occipital horn syndrome, Tranebjaerg–Svejgaard syndrome, X-linked myotubular myopathy, Hyper-IgM syndrome type 1, Wu syndrome, Gustavson syndrome, Retinoschisis, Adrenoleukodystrophy, Wilson–Turner syndrome, Spinal and bulbar muscular atrophy, X-linked endothelial corneal dystrophy, Simpson–Golabi–Behmel syndrome, HNRNPH2-related disorders

Smith–Fineman–Myers syndrome, TBX22, Blue-cone monochromacy, Sperm protein associated with the nucleus, X-linked, family member A1, DDX3X syndrome, Nonsyndromic deafness, PHF8, Conradi–Hünermann syndrome, Hypohidrotic ectodermal dysplasia, Congenital stationary night blindness, Allan–Herndon–Dudley syndrome, Genetic disorder, Snyder–Robinson syndrome, Sideroblastic anemia, Neural tube defect, Muscular dystrophy, Brunner syndrome, 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, 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, Telegram (software), C0 and C1 control codes, Neutropenia, Heart valve dysplasia, Dwarfism, Tetra-amelia syndrome, Hair loss, Internet in South Africa, VMware ThinApp, Template_talk:Military_ranks

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 severe combined immunodeficiency, X-linked ichthyosis, 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, Occipital horn syndrome, Tranebjaerg–Svejgaard syndrome, X-linked myotubular myopathy, Hyper-IgM syndrome type 1, Wu syndrome, Gustavson syndrome, Retinoschisis, Adrenoleukodystrophy, Wilson–Turner syndrome, Spinal and bulbar muscular atrophy, X-linked endothelial corneal dystrophy, Simpson–Golabi–Behmel syndrome, HNRNPH2-related disorders, Smith–Fineman–Myers syndrome, TBX22, Blue-cone monochromacy, Sperm protein associated with the nucleus, X-linked, family member A1, DDX3X syndrome, Nonsyndromic deafness, PHF8, Conradi–Hünermann syndrome, Hypohidrotic ectodermal dysplasia, Congenital stationary night blindness, Allan–Herndon–Dudley syndrome, Genetic disorder, Snyder–Robinson syndrome, Sideroblastic anemia, Neural tube defect, Muscular dystrophy, Brunner syndrome, 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, 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, Telegram (software), C0 and C1 control codes, Neutropenia, Heart valve dysplasia, 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