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
Assertion criteria
Level: Assertion criteria not provided
Summary of submissions to ClinVar
Total submissions: 46
Gene
Gene | Submissions | Last Updated |
---|
ABCC8 | 1 | Apr 23, 2024 |
ABCG5 | 1 | Nov 16, 2021 |
ABCG8 | 1 | Nov 16, 2021 |
APC | 1 | Jan 26, 2021 |
BBS2 | 1 | Oct 22, 2023 |
CASR | 1 | May 16, 2022 |
COL4A4 | 1 | Jul 6, 2024 |
COL4A5 | 3 | Mar 7, 2024 |
CYB5R3 | 2 | Feb 17, 2024 |
CYP2U1 | 1 | Jul 25, 2024 |
DNAJB11 | 1 | Apr 29, 2024 |
EHMT1 | 1 | Apr 13, 2024 |
ENG | 1 | Nov 6, 2022 |
FANCA | 2 | Apr 16, 2024 |
FH | 1 | Nov 15, 2022 |
FLCN | 1 | Nov 15, 2022 |
FPGT-TNNI3K | 1 | Apr 19, 2024 |
GBA1 | 2 | Nov 2, 2023 |
GSN | 1 | Jul 11, 2023 |
LDLR | 2 | Feb 25, 2022 |
LIPA | 1 | Sep 28, 2023 |
LMX1B | 1 | Jul 6, 2024 |
LOC106627981 | 2 | Nov 2, 2023 |
LOC651337 | 1 | Apr 13, 2024 |
LZTR1 | 1 | Sep 28, 2023 |
MTHFR | 1 | Mar 6, 2022 |
NF1 | 1 | Jun 2, 2022 |
NOTCH1 | 1 | Jul 11, 2023 |
NPHS1 | 2 | Nov 15, 2022 |
PHEX | 2 | Aug 20, 2021 |
PKLR | 1 | Jun 28, 2023 |
PLOD2 | 1 | Sep 8, 2021 |
POLR3A | 1 | Jun 20, 2023 |
PROS1 | 1 | May 4, 2021 |
PTCHD1-AS | 1 | Oct 10, 2017 |
RAB11B | 1 | May 21, 2024 |
SCN5A | 2 | Apr 10, 2024 |
SLC12A3 | 1 | Mar 6, 2021 |
SLC7A7 | 1 | Mar 6, 2022 |
SLCO1B1 | 1 | May 26, 2022 |
TENM4 | 1 | Mar 14, 2022 |
TNNI3K | 1 | Apr 19, 2024 |
Condition
Name | Submissions | Last Updated | Alport syndrome | 3 | Mar 7, 2024 |
Aortic valve disease 1 | 1 | Jul 11, 2023 |
Atrial conduction disease | 1 | Apr 19, 2024 |
Autosomal dominant Alport syndrome | 1 | Jul 6, 2024 |
Autosomal dominant polycystic kidney disease | 1 | Apr 29, 2024 |
Bardet-Biedl syndrome 2 | 1 | Oct 22, 2023 |
Birt-Hogg-Dube syndrome | 1 | Nov 15, 2022 |
Bruck syndrome 2 | 1 | Sep 8, 2021 |
Brugada syndrome | 1 | Oct 2, 2021 |
Congenital and infantile nephrotic syndrome | 1 | Nov 15, 2022 |
Familial X-linked hypophosphatemic vitamin D refractory rickets | 1 | Aug 20, 2021 |
Familial adenomatous polyposis 1 | 1 | Jan 26, 2021 |
Familial hypocalciuric hypercalcemia 1 | 1 | May 16, 2022 |
Familial hypokalemia-hypomagnesemia | 1 | Mar 6, 2021 |
Fanconi anemia | 2 | Apr 16, 2024 |
Finnish congenital nephrotic syndrome | 1 | Nov 6, 2022 |
Finnish type amyloidosis | 1 | Jul 11, 2023 |
Gaucher disease type I | 2 | Nov 2, 2023 |
Hereditary leiomyomatosis and renal cell cancer | 1 | Nov 15, 2022 |
Hereditary methemoglobinemia | 2 | Feb 17, 2024 |
Hereditary spastic paraplegia 56 | 1 | Jul 25, 2024 |
Hypercholesterolemia, familial, 1 | 2 | Feb 25, 2022 |
Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome | 1 | Jun 20, 2023 |
Kleefstra syndrome | 1 | Apr 13, 2024 |
Lysinuric protein intolerance | 1 | Mar 6, 2022 |
Lysosomal acid lipase deficiency | 1 | Sep 28, 2023 |
Maturity onset diabetes mellitus in young | 1 | Apr 23, 2024 |
Nail-patella-like renal disease | 1 | Jul 6, 2024 |
Neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter | 1 | May 21, 2024 |
Neurofibromatosis, type 1 | 1 | Jun 2, 2022 |
Progressive familial heart block, type 1A | 1 | Apr 10, 2024 |
Pyruvate kinase deficiency of red cells | 1 | Jun 28, 2023 |
Rotor syndrome | 1 | May 26, 2022 |
Schwannomatosis 2 | 1 | Sep 28, 2023 |
Sitosterolemia | 1 | Nov 16, 2021 |
Telangiectasia, hereditary hemorrhagic, type 1 | 1 | Nov 6, 2022 |
Thrombophilia due to protein S deficiency, autosomal dominant | 1 | May 4, 2021 |
Thrombophilia due to thrombin defect | 1 | Mar 6, 2022 |
Tremor, hereditary essential, 5 | 1 | Mar 14, 2022 |
Vitamin D-dependent rickets, type 2 | 1 | Oct 10, 2017 |