X-linked spinal muscular atrophy 2Redirect to: Information related to X-linked spinal muscular atrophy 2Sex 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, IPEX syndrome, Tranebjaerg–Svejgaard syndrome, 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hypogonadism, Satellaview, Situs inversus, Nystagmus, Hypoparathyroidism, XMODEM, Spinocerebellar ataxia, Aortic arches, Hereditary spastic paraplegia, Ectrodactyly, URL shortening, Mitral valve prolapse, Senran Kagura, List of Super Robot Wars video games, Retinal dysplasia, Arthrogryposis, Neutropenia, C0 and C1 control codes, Telegram (software), 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 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, IPEX syndrome, Tranebjaerg–Svejgaard syndrome, Occipital horn syndrome, X-linked myotubular myopathy, Hyper-IgM syndrome type 1, Fragile X syndrome, Gustavson syndrome, Wu syndrome, Adrenoleukodystrophy, Retinoschisis, Wilson–Turner syndrome, X-linked endothelial corneal dystrophy, HNRNPH2-related disorders, Spinal and bulbar muscular atrophy, Simpson–Golabi–Behmel syndrome, Smith–Fineman–Myers syndrome, TBX22, DDX3X syndrome, Sperm protein associated with the nucleus, X-linked, family member A1, Blue-cone monochromacy, PHF8, Nonsyndromic deafness, Conradi–Hünermann syndrome, Hypohidrotic ectodermal dysplasia, Congenital stationary night blindness, Allan–Herndon–Dudley syndrome, 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