Genetic diseases-X

• X chromosome-linked sideroblastic anemia see X-linked sideroblastic anemia
• X linked Recessive Hereditary Spastic Paraplegia see Spastic paraplegia type 2
• X-ALD see X-linked adrenoleukodystrophy
• X-LAG see X-linked acrogigantism
• X-linked acrogigantism
• X-linked acrogigantism syndrome see X-linked acrogigantism
• X-linked adrenal hypoplasia congenita
• X-linked adrenoleukodystrophy
• X-linked agammaglobulinemia
• X-linked AHC see X-linked adrenal hypoplasia congenita
• X-linked alpha-thalassemia/mental retardation syndrome see Alpha thalassemia X-linked intellectual disability syndrome
• X-linked arthrogryposis multiplex congenita see X-linked infantile spinal muscular atrophy
• X-linked arthrogryposis type I see X-linked infantile spinal muscular atrophy
• X-linked autoimmunity-allergic dysregulation syndrome see Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome
• X-linked cardiac valvular dysplasia
• X-linked centronuclear myopathy see X-linked myotubular myopathy
• X-linked chondrodysplasia punctata 1
• X-linked chondrodysplasia punctata 2
• X-linked chronic granulomatous disease see Chronic granulomatous disease
• X-linked congenital nystagmus see X-linked infantile nystagmus
• X-linked congenital stationary night blindness
• X-linked copper deficiency see Menkes syndrome
• X-linked creatine deficiency
• X-linked creatine deficiency syndrome see X-linked creatine deficiency
• X-linked CSNB see X-linked congenital stationary night blindness
• X-linked dilated cardiomyopathy
• X-linked dominant chondrodysplasia punctata see X-linked chondrodysplasia punctata 2
• X-linked dystonia-parkinsonism
• X-linked dystonia-parkinsonism syndrome see X-linked dystonia-parkinsonism
• X-linked hydrocephalus syndrome see L1 syndrome
• X-linked hyper IgM syndrome
• X-linked hypergonadotropic ovarian failure see Fragile X-associated primary ovarian insufficiency
• X-linked hyperuricemia see Lesch-Nyhan syndrome
• X-linked idiopathic infantile nystagmus see X-linked infantile nystagmus
• X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia
• X-linked infantile nystagmus
• X-linked infantile spasm syndrome see Early infantile epileptic encephalopathy 1
• X-linked infantile spasm syndrome 1 see Early infantile epileptic encephalopathy 1
• X-linked infantile spinal muscular atrophy
• X-linked intellectual deficit due to PQBP1 mutations see Renpenning syndrome
• X-linked intellectual deficit with marfanoid habitus see Lujan syndrome
• X-linked intellectual deficit, Najm type see CASK-related intellectual disability
• X-linked intellectual deficit, Renpenning type see Renpenning syndrome
• X-linked intellectual deficit-dystonia-dysarthria see Partington syndrome
• X-linked intellectual disability, Siderius type
• X-linked juvenile retinoschisis
• X-linked lethal infantile SMA see X-linked infantile spinal muscular atrophy
• X-linked lissencephaly 2 see X-linked lissencephaly with abnormal genitalia
• X-linked lissencephaly with abnormal genitalia
• X-linked lissencephaly with ambiguous genitalia see X-linked lissencephaly with abnormal genitalia
• X-linked lymphoproliferative disease
• X-linked lymphoproliferative syndrome see X-linked lymphoproliferative disease
• X-linked macrothrombocytopenia see Dyserythropoietic anemia and thrombocytopenia
• X-linked mental retardation and macroorchidism see Fragile X syndrome
• X-linked mental retardation Hamel type see X-linked intellectual disability, Siderius type
• X-linked mental retardation Siderius type see X-linked intellectual disability, Siderius type
• X-linked mental retardation with dystonic movements, ataxia, and seizures see Partington syndrome
• X-linked mental retardation with marfanoid habitus see Lujan syndrome
• X-linked mental retardation, syndromic 13 see PPM-X syndrome
• X-linked monoamine oxidase deficiency see Monoamine oxidase A deficiency
• X-linked myotubular myopathy
• X-linked myxomatous valvular dystrophy see X-linked cardiac valvular dysplasia
• X-linked Ohdo syndrome see Ohdo syndrome, Maat-Kievit-Brunner type
• X-linked Ohtahara syndrome see Early infantile epileptic encephalopathy 1
• X-linked primary hyperuricemia see Lesch-Nyhan syndrome
• X-linked pyridoxine-responsive sideroblastic anemia see X-linked sideroblastic anemia
• X-linked recessive chondrodysplasia punctata 1 see X-linked chondrodysplasia punctata 1
• X-linked retinoschisis see X-linked juvenile retinoschisis
• X-linked SCID see X-linked severe combined immunodeficiency
• X-linked SED see X-linked spondyloepiphyseal dysplasia tarda
• X-linked SEDT see X-linked spondyloepiphyseal dysplasia tarda
• X-linked severe combined immunodeficiency
• X-linked sideroblastic anemia
• X-linked sideroblastic anemia and ataxia
• X-linked spinal and bulbar muscular atrophy see Spinal and bulbar muscular atrophy
• X-linked spondyloepiphyseal dysplasia tarda
• X-linked thrombocytopenia
• X-linked torsion dystonia-parkinsonism syndrome see X-linked dystonia-parkinsonism
• X-linked uric aciduria enzyme defect see Lesch-Nyhan syndrome
• X-linked West syndrome see Early infantile epileptic encephalopathy 1
• X-SCID see X-linked severe combined immunodeficiency
• xanthine dehydrogenase deficiency see Hereditary xanthinuria
• xanthine oxidase deficiency see Hereditary xanthinuria
• xanthinuria see Hereditary xanthinuria
• XDH deficiency see Hereditary xanthinuria
• XDP see X-linked dystonia-parkinsonism
• Xeroderma pigmentosum
• XGS see Xia-Gibbs syndrome
• Xia-Gibbs syndrome
• XJR see X-linked juvenile retinoschisis
• XL-SMA see X-linked infantile spinal muscular atrophy
• XLA see X-linked agammaglobulinemia
• XLAAD see Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome
• XLAG see X-linked lissencephaly with abnormal genitalia
• XLAG see X-linked acrogigantism
• XLCM see X-linked dilated cardiomyopathy
• XLCSNB see X-linked congenital stationary night blindness
• XLDC see X-linked dilated cardiomyopathy
• XLISG see X-linked lissencephaly with abnormal genitalia
• XLMR with marfanoid features see Lujan syndrome
• XLMR-hypotonic face syndrome see Alpha thalassemia X-linked intellectual disability syndrome
• XLMTM see X-linked myotubular myopathy
• XLOA see Ocular albinism
• XLP see X-linked lymphoproliferative disease
• XLSA see X-linked sideroblastic anemia
• XLSA/A see X-linked sideroblastic anemia and ataxia
• XLSMA see X-linked infantile spinal muscular atrophy
• XLT see X-linked thrombocytopenia
• XMEN see X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia
• XMTM see X-linked myotubular myopathy
• XMVD see X-linked cardiac valvular dysplasia
• XP see Xeroderma pigmentosum
• XSCID see X-linked severe combined immunodeficiency
• XX male syndrome see 46,XX testicular disorder of sex development
• XX sex reversal see 46,XX testicular disorder of sex development
• XXX syndrome see Triple X syndrome
• XXXXY aneuploidy see 49,XXXXY syndrome
• XXXXY syndrome see 49,XXXXY syndrome
• XXXY males see 48,XXXY syndrome
• XXXY syndrome see 48,XXXY syndrome
• XXY syndrome see Klinefelter syndrome
• XXY trisomy see Klinefelter syndrome
• XXYY syndrome see 48,XXYY syndrome
• XY pure gonadal dysgenesis see Swyer syndrome
• xylitol dehydrogenase deficiency see Essential pentosuria
• XYY karyotype see 47,XYY syndrome
• XYY syndrome see 47,XYY syndrome