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GENE - TERM ANNOTATION REPORT

RGD ID: 8740878
Species: Chinchilla lanigera
RGD Object: Gene
Symbol: Fgg
Name: fibrinogen gamma chain
Acc ID: DOID:2236
Term: congenital afibrinogenemia
Definition: A blood coagulation disease that is characterized by an impaired blood clotting resulting from a lack deficiency of a the fibrinogen protein (coagulation factor I). (DO)
Definition Source(s): https://ghr.nlm.nih.gov/condition/congenital-afibrinogenemia#synonyms "DO" "DO"
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
Fgg ISOFGG (Homo sapiens)7240710OMIM  
Fgg ISOFGG (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Afibrinogenemia | ClinVar Annotator: match by term: Congenital afibrinogenemia | ClinVar Annotator: match by term: FIBRINOGEN PARIS 1 | ClinVar Annotator: match by term: HypofibrinogenemiaPMID:10688828 PMID:10911375 PMID:11001902 PMID:11001903 PMID:11435303 PMID:1249208 PMID:1471077 PMID:15795540 PMID:16144795 PMID:1733971 PMID:17650452 PMID:17849064 PMID:17854317 PMID:17938819 PMID:19300242 PMID:21228398 PMID:21725578 PMID:23061815 PMID:23560673 PMID:24033266 PMID:24556703 PMID:25039884 PMID:2512677 PMID:25320241 PMID:25741868 PMID:26105150 PMID:2617471 PMID:28211264 PMID:28492532 PMID:29240685 PMID:29351094 PMID:2971042 PMID:2976995 PMID:30349899 PMID:30418131 PMID:30431218 PMID:30487145 PMID:30632992 PMID:31064749 PMID:31295712 PMID:31352677 PMID:31479941 PMID:32852326 PMID:32877852 PMID:3337908 PMID:33443927 PMID:33477601 PMID:34275736 PMID:34355501 PMID:3563970 PMID:35809055 PMID:35853369 PMID:37583269 PMID:4002201 PMID:4427684 PMID:6654188 PMID:6886002 PMID:7635941 PMID:7654933 PMID:8470043
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