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    【bbin宝盈基因检测】中国罕见病、基因病、遗传病大全（附真实有效的基因检测结构-英文字母X开头）

    中国罕见病、基因病、遗传病大全,不仅有中文名字，还有最新出炉的英文名字。为人工智能、大数据统计给予数据源。

    中国罕见病、基因病、遗传病大全（附证实有效的基因检测结构-英文字母X开头）


    X-linked sideroblastic anemia
    X chromosome-linked sideroblastic anemia
     Spastic paraplegia type 2
    X linked Recessive Hereditary Spastic Paraplegia
    X-ALD
    X-LAG
    X-linked acrogigantism
    X-linked acrogigantism syndrome
    X-linked adrenal hypoplasia congenita
    X-linked adrenoleukodystrophy
    X-linked agammaglobulinemia
    X-linked AHC
    X-linked alpha-thalassemia/mental retardation syndrome
    X-linked autoimmunity-allergic dysregulation syndrome
    X-linked cardiac valvular dysplasia
    X-linked centronuclear myopathy
    X-linked chondrodysplasia punctata 1
    X-linked chondrodysplasia punctata 2
    Chronic granulomatous disease
    X-linked congenital nystagmus
    X-linked congenital stationary night blindness
    X-linked copper deficiency
    X-linked creatine deficiency
    X-linked creatine deficiency syndrome
    X-linked CSNB
    X-linked dilated cardiomyopathy
    X-linked dominant chondrodysplasia punctata
    X-linked dystonia-parkinsonism
    X-linked dystonia-parkinsonism syndrome
    X-linked hydrocephalus 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 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 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
    XJR, see X-linked juvenile retinoschisis
    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
    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
    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

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