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Department of Traditional Chinese Medicine (Fujian Provincial Hospital)

General information

Department of Traditional Chinese Medicine
Fujian Provincial Hospital
No.134 Dongjie
Fuzhou
China - 350001

Organization ID: 506270

Personnel

Assertion criteria

Level: Assertion criteria not provided

    Summary of submissions to ClinVar

    Total submissions: 46

    Gene

    GeneSubmissionsLast Updated
    ABCC81Apr 23, 2024
    ABCG51Nov 16, 2021
    ABCG81Nov 16, 2021
    APC1Jan 26, 2021
    BBS21Oct 22, 2023
    CASR1May 16, 2022
    COL4A41Jul 6, 2024
    COL4A53Mar 7, 2024
    CYB5R32Feb 17, 2024
    CYP2U11Jul 25, 2024
    DNAJB111Apr 29, 2024
    EHMT11Apr 13, 2024
    ENG1Nov 6, 2022
    FANCA2Apr 16, 2024
    FH1Nov 15, 2022
    FLCN1Nov 15, 2022
    FPGT-TNNI3K1Apr 19, 2024
    GBA12Nov 2, 2023
    GSN1Jul 11, 2023
    LDLR2Feb 25, 2022
    LIPA1Sep 28, 2023
    LMX1B1Jul 6, 2024
    LOC1066279812Nov 2, 2023
    LOC6513371Apr 13, 2024
    LZTR11Sep 28, 2023
    MTHFR1Mar 6, 2022
    NF11Jun 2, 2022
    NOTCH11Jul 11, 2023
    NPHS12Nov 15, 2022
    PHEX2Aug 20, 2021
    PKLR1Jun 28, 2023
    PLOD21Sep 8, 2021
    POLR3A1Jun 20, 2023
    PROS11May 4, 2021
    PTCHD1-AS1Oct 10, 2017
    RAB11B1May 21, 2024
    SCN5A2Apr 10, 2024
    SLC12A31Mar 6, 2021
    SLC7A71Mar 6, 2022
    SLCO1B11May 26, 2022
    TENM41Mar 14, 2022
    TNNI3K1Apr 19, 2024

    Condition

    NameSubmissionsLast Updated
    Alport syndrome3Mar 7, 2024
    Aortic valve disease 11Jul 11, 2023
    Atrial conduction disease1Apr 19, 2024
    Autosomal dominant Alport syndrome1Jul 6, 2024
    Autosomal dominant polycystic kidney disease1Apr 29, 2024
    Bardet-Biedl syndrome 21Oct 22, 2023
    Birt-Hogg-Dube syndrome1Nov 15, 2022
    Bruck syndrome 21Sep 8, 2021
    Brugada syndrome1Oct 2, 2021
    Congenital and infantile nephrotic syndrome1Nov 15, 2022
    Familial X-linked hypophosphatemic vitamin D refractory rickets1Aug 20, 2021
    Familial adenomatous polyposis 11Jan 26, 2021
    Familial hypocalciuric hypercalcemia 11May 16, 2022
    Familial hypokalemia-hypomagnesemia1Mar 6, 2021
    Fanconi anemia2Apr 16, 2024
    Finnish congenital nephrotic syndrome1Nov 6, 2022
    Finnish type amyloidosis1Jul 11, 2023
    Gaucher disease type I2Nov 2, 2023
    Hereditary leiomyomatosis and renal cell cancer1Nov 15, 2022
    Hereditary methemoglobinemia2Feb 17, 2024
    Hereditary spastic paraplegia 561Jul 25, 2024
    Hypercholesterolemia, familial, 12Feb 25, 2022
    Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome1Jun 20, 2023
    Kleefstra syndrome1Apr 13, 2024
    Lysinuric protein intolerance1Mar 6, 2022
    Lysosomal acid lipase deficiency1Sep 28, 2023
    Maturity onset diabetes mellitus in young1Apr 23, 2024
    Nail-patella-like renal disease1Jul 6, 2024
    Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter1May 21, 2024
    Neurofibromatosis, type 11Jun 2, 2022
    Progressive familial heart block, type 1A1Apr 10, 2024
    Pyruvate kinase deficiency of red cells1Jun 28, 2023
    Rotor syndrome1May 26, 2022
    Schwannomatosis 21Sep 28, 2023
    Sitosterolemia1Nov 16, 2021
    Telangiectasia, hereditary hemorrhagic, type 11Nov 6, 2022
    Thrombophilia due to protein S deficiency, autosomal dominant1May 4, 2021
    Thrombophilia due to thrombin defect1Mar 6, 2022
    Tremor, hereditary essential, 51Mar 14, 2022
    Vitamin D-dependent rickets, type 21Oct 10, 2017