X-Linked mental retardation

Sex linkage, X-linked dominant inheritance, X-linked intellectual disability, X-linked recessive inheritance, X-linked thrombocytopenia, 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, IPEX syndrome, Occipital horn syndrome, Tranebjaerg–Svejgaard syndrome, X-linked myotubular myopathy, Hyper-IgM syndrome type 1, Fragile X syndrome, Gustavson syndrome, Wu syndrome, Adrenoleukodystrophy, Retinoschisis, Wilson–Turner syndrome, Spinal and bulbar muscular atrophy, X-linked endothelial corneal dystrophy, HNRNPH2-related disorders, 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, 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, Brunner syndrome, Muscular dystrophy, Charcot–Marie–Tooth disease, Aqueductal stenosis, Leigh syndrome, Object Linking and Embedding, Lesch–Nyhan syndrome, Emery–Dreifuss muscular dystrophy, Situs ambiguus, Hypogonadotropic hypogonadism, Familial exudative vitreoretinopathy, Situs inversus, Nystagmus, Satellaview, Hypoparathyroidism, XMODEM, Spinocerebellar ataxia, Aortic arches, Hereditary spastic paraplegia, Ectrodactyly, URL shortening, Mitral valve prolapse, Senran Kagura, Arthrogryposis, List of Super Robot Wars video games, Retinal dysplasia, Neutropenia, Telegram (software), C0 and C1 control codes, Heart valve dysplasia, Dwarfism, Tetra-amelia syndrome, Hair loss, Internet in South Africa, VMware ThinApp

Sex linkage, X-linked dominant inheritance, X-linked intellectual disability, X-linked recessive inheritance, X-linked thrombocytopenia, 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, IPEX syndrome, Occipital horn syndrome, Tranebjaerg–Svejgaard syndrome, X-linked myotubular myopathy, Hyper-IgM syndrome type 1, Fragile X syndrome, Gustavson syndrome, Wu syndrome, Adrenoleukodystrophy, Retinoschisis, Wilson–Turner syndrome, Spinal and bulbar muscular atrophy, X-linked endothelial corneal dystrophy, HNRNPH2-related disorders, 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, 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, Brunner syndrome, Muscular dystrophy, Charcot–Marie–Tooth disease, Aqueductal stenosis, Leigh syndrome, Object Linking and Embedding, Lesch–Nyhan syndrome, Emery–Dreifuss muscular dystrophy, Situs ambiguus, Hypogonadotropic hypogonadism, Familial exudative vitreoretinopathy, Situs inversus, Nystagmus, Satellaview, Hypoparathyroidism, XMODEM, Spinocerebellar ataxia, Aortic arches, Hereditary spastic paraplegia, Ectrodactyly, URL shortening, Mitral valve prolapse, Senran Kagura, Arthrogryposis, List of Super Robot Wars video games, Retinal dysplasia, Neutropenia, Telegram (software), C0 and C1 control codes, Heart valve dysplasia, Dwarfism, Tetra-amelia syndrome, Hair loss, Internet in South Africa, VMware ThinApp, Peregrina, منعكس_بدائي, Daftar_Duta_Besar_Indonesia_untuk_Argentina, Interview_with_the_Vampire_(TV_series), 2014_NCAA_Division_I_FBS_football_rankings, 襟裳_(給油艦), Bookend, Шахта_імені_Фрунзе_(Кривбас), Maximinus_dari_Trier, Ozan_Tufan, Isekai_de_Chīto_Sukiru_o_Te_ni_Shita_Ore_wa,_Genjitsu_Sekai_o_mo_Musō_Suru:_Reberu_Appu_wa_Jinsei_o_Kaeta, Irwansyah_(politikus), Нарушения_и_недисциплинированное_поведение_(футбол), Estação_Ferroviária_de_Benfica, ボビー・ウーマック, プロイセン公国, Паспорт_гражданина_Абхазии, 1992_Kids'_Choice_Awards, Dedy_Ermansyah, Шервиллер, جوناثون_سولومون, List_of_Billboard_Hot_100_top-ten_singles_in_2010, كين_ويفر_(سائق_سباق), خط_طول_102°_شرق, Canton_of_Chemillé-en-Anjou, Hell's_Kitchen_(American_season_7), مدلاين_بلس, Lao_People's_Liberation_Army_Air_Force, Hong_Kong, Suku_Lani, Margaret_Howard,_Countess_of_Nottingham, عملية_إنقاذ_الرهائن_في_اليمن_(2014), Collegio_di_East_Antrim, Zimbabwe_pada_Olimpiade, Kai_Bird, Los_Cerritos_Center, Ying_Yong, ثورة_جانكيس, Didier_Deschamps, I_Want_You_So_Bad, Buddhist_Studies_Review, Pakubuwana_XII, North_Philadelphia_station_(Broad_Street_Line), بوابة:بنية_تحتية, كاتي_جاي_ستون, Sri_Lanka–United_Kingdom_relations, Gobierno_Kristersson, VSB_–_Technical_University_of_Ostrava, Азербайджанский_национальный_костюм, Maria_Nagai, Judge_Dredd:_The_Role-Playing_Game, MTV, Barack_Obama_Supreme_Court_candidates, One_Day_(Matisyahu_song), Zany_Golf, Scuderia_AlphaTauri, Athletics_at_the_1912_Summer_Olympics_–_Men's_marathon, 安芸太田町, Ina,_Kapatid,_Anak, Rachel_Wall