X-linked

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, Snyder–Robinson syndrome, Genetic disorder, Sideroblastic anemia, Brunner syndrome, Muscular dystrophy, Charcot–Marie–Tooth disease, Neural tube defect, Aqueductal stenosis, Leigh syndrome, Object Linking and Embedding, Lesch–Nyhan syndrome, Emery–Dreifuss muscular dystrophy, Situs ambiguus, Hypogonadotropic hypogonadism, Familial exudative vitreoretinopathy, Satellaview, Situs inversus, Nystagmus, Hypoparathyroidism, Aortic arches, Hereditary spastic paraplegia, 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, ペペ_(映画), عبد_العزيز_العروي, Landvetter

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, Snyder–Robinson syndrome, Genetic disorder, Sideroblastic anemia, Brunner syndrome, Muscular dystrophy, Charcot–Marie–Tooth disease, Neural tube defect, Aqueductal stenosis, Leigh syndrome, Object Linking and Embedding, Lesch–Nyhan syndrome, Emery–Dreifuss muscular dystrophy, Situs ambiguus, Hypogonadotropic hypogonadism, Familial exudative vitreoretinopathy, Satellaview, Situs inversus, Nystagmus, Hypoparathyroidism, Aortic arches, Hereditary spastic paraplegia, 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, ペペ_(映画), عبد_العزيز_العروي, Landvetter, Люм'єр_(кінотеатр,_Івано-Франківськ), Katharine_Ross, Regio_II_Caelimontium, متغير_العملية, Outline_of_the_State_of_Palestine, Jean-Baptiste_Hugues, Nevada_State_Route_562, ラッシュ時, فيكتوريا_مارينوفا, Песчаный_Умёт, MIN_Timpik, Kleptoparasitism, Halterofilismo_nos_Jogos_Olímpicos_de_Verão_da_Juventude_de_2010_-_Até_62_kg_masculino, List_of_Dr._Slump_films, Джаниев,_Ровшан_Рафик_оглы, President's_House_(University_of_Florida), Red_Wings_Airlines_Flight_9268, ECAM_LaSalle, Olivier_De_Schutter, Realart_Pictures_Inc., Mining_industry_of_the_Gambia, Abdul_Wahid_Hasyim, Produce_Camp_2019, Iron_Curtain, The_Last_Time_(All_That_Remains_song), Richard_J._Berry, 上峰町, Симфонія_№_37_(Моцарт), بيت_أبو_مرعى_(أرحب), Tikus_Desa_dan_Tikus_Kota, Нападение_в_джунглях, The_Miraculous_Draught_of_Fishes_(Jordaens), Mi_wonton, Istana_Stockholm, Kimberley_Echo, ショーン・チャコーン, Judo, Dodge_50_Series, SMA_Negeri_8_Medan, Кабрал_ди_Мелу_Нету,_Жуан, Currys_Digital, George_I_of_Great_Britain, Rumah_tradisional_Perak, Swing_Kids_(2018_film), شابة_وجميلة_(فيلم), Райс,_Энгаури, تنفس_بطني, Margaret_(film), Bantarkawung,_Brebes, help:referencing_for_beginners, Limón_de_San_Lucas_del_Maíz, Dance_Evolution, Giampaolo_Pansa, Предсказание_структуры_белка, Say_Something_(A_Great_Big_World_song), Living_(2012_film), Ab_Khvor, 2014_MLS_All-Star_Game, Johann_Gottfried_Herder, Ralph_Belknap_Baldwin