Summaries for Hypofibrinogenemia

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44Wikipedia, 22MalaCards
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Wikipedia: Fibrinolysis syndrome (also known as \"Defibrinating syndrome,\" and \"Hypofibrinogenemia\") is...44 more...

MalaCards: Hypofibrinogenemia is related to von willebrand's disease and dysfibrinogenemia. An important gene associated with Hypofibrinogenemia is FGG (fibrinogen gamma chain), and among its related pathways are Cell adhesion_Integrin inside-out signaling and Metalloproteases in connective tissue degradation. The compounds clopidogrel and hepaplastin have been mentioned in the context of this disorder. Affiliated tissues include skin, and related mouse phenotypes are hematopoietic system and immune system.

Aliases & Descriptions for Hypofibrinogenemia

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7diseasecard, 32Novoseek , 43UMLS
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hypofibrinogenemia 7 32 43

Related Diseases for Hypofibrinogenemia

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13GeneCards, 14GeneDecks
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Diseases related to hypofibrinogenemia by text searches and GeneDecks gene sharing:

(show top 50)    (show all 353)
idRelated DiseaseScoreTop Affiliating Genes
1von willebrand's disease28.0VWF, F3, F2
2dysfibrinogenemia26.3SERPINC1, FGA, FGB, FGG, F2, ALB
3thrombophilia25.1VWF, SERPINC1, SERPINF2, SERPINE1, FGA, FGB
4hepatitis23.1VWF, SERPINC1, SERPINF2, SERPINE1, FGA, FGB
5thrombophilia, dysfibrinogenemic13.6FGB, FGG
6afibrinogenemia13.6FGA, FGB
7hereditary amyloidosis13.5FGA, APOA1
8thrombosis13.4FGB, F2
9factor xii deficiency13.4F3, F2
10factor x deficiency13.4F3, F2
11prothrombin deficiency13.4SERPINC1, F2
12lymphoplasmacytic lymphoma13.4F3, F2
13alpha-1-antichymotrypsin deficiency13.4SERPINC1, SERPINF2
14hyperprothrombinemia13.4SERPINC1, F2
15factor v deficiency13.4F3, F2
16spinal cord infarction13.4SERPINC1, F2
17sagittal sinus thrombosis13.4SERPINC1, F3
18hantavirus pulmonary syndrome13.3F3, F2
19central serous chorioretinopathy13.3SERPINE1, PLAT
20intracranial embolism13.3SERPINC1, PLAT
21ruptured abdominal aortic aneurysm13.3F3, F2
22acute biphenotypic leukemia13.3F3, F2
23vein disease13.3SERPINC1, F2
24plasminogen activator inhibitor type 1 deficiency13.3SERPINE1, PLAT
25plasminogen activator deficiency13.3SERPINE1, PLAT
26vitamin k deficiency hemorrhagic disease13.3F3, F2
27type 3 von willebrand disease13.3VWF, PLAT
28sneddon syndrome13.2SERPINC1, F2
29apo a-i deficiency13.2APOA1, ALB
30thromboangiitis obliterans13.2SERPINE1, PLAT
31familial hypertriglyceridemia13.2SERPINE1, APOA1
32antithrombin iii deficiency13.2SERPINC1, FGA, F2
33hepatic tuberculosis13.2F2, ALB
34coronary stenosis13.2SERPINE1, FGA, APOA1
35cerebral hemorrhage13.1SERPINF2, F2, PLAT
36vericose veins13.1F2, ALB
37peripheral vertigo13.1SERPINC1, F3, F2
38warfarin resistance13.1F2, ALB
39catastrophic antiphospholipid syndrome13.1SERPINE1, F3
40esophageal varix13.1F2, ALB
41acute myocarditis13.1FGA, PLAT
42bernard-soulier syndrome13.1VWF, FGA, F2
43factor vii deficiency13.1SERPINC1, F3, F2
44intracranial thrombosis13.1SERPINC1, F2, PLAT
45sycp3-related pregnancy loss, susceptibility to13.1SERPINC1, F3, F2
46acquired von willebrand syndrome13.1VWF, F3, F2
47neonatal stroke13.1SERPINE1, ALB
48hemarthrosis13.1VWF, F3, F2
49moyamoya disease13.1SERPINC1, F3, F2
50hypersplenism13.1F2, ALB

Graphical network of the top 20 diseases related to hypofibrinogenemia:



Graphical network of diseases related to hypofibrinogenemia

Clinical Features for Hypofibrinogenemia

Drugs & Therapeutics for Hypofibrinogenemia

Sources:
4CenterWatch, 29NIH Clinical Center, 5ClinicalTrials, 43UMLS, 28NDF-RT
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Approved drugs:

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Drug clinical trials:

Search ClinicalTrials for hypofibrinogenemia

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Genetic Tests for Hypofibrinogenemia

Anatomical Context for Hypofibrinogenemia

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22MalaCards
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MalaCards organs/tissues related to hypofibrinogenemia:

22
Skin

Phenotypes for genes affiliated with Hypofibrinogenemia

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25MGI
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MGI Mouse Phenotypes related to hypofibrinogenemia:

25
idDescriptionMGI Source AccessionScoreTop Affiliating Genes
1hematopoietic system phenotypeMP:00053979.9UNC13D, FGG
2immune system phenotypeMP:00053878.7VWF, APOA1, F2, PLAT, UNC13D
3liver/biliary system phenotypeMP:00053707.9SERPINC1, SERPINE1, FGA, APOA1, ALB, CP
4cardiovascular system phenotypeMP:00053856.8APOA1, VWF, F3, FGG, FGA, SERPINE1
5mortality/agingMP:00107686.7PRF1, PLAT, ALB, F2, VWF, SERPINC1
6homeostasis/metabolism phenotypeMP:00053765.6APOA1, FGG, FGA, F3, SERPINF2, SERPINC1

Publications for genes affiliated with Hypofibrinogenemia

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35PubMed
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Articles related to hypofibrinogenemia:

idTitleAuthorsYearAffiliating Genes
1Congenital hypofibrinogenemia: characterization of two missense mutations affecting fibrinogen assembly and secretion. (18676163)Plate M.... Duga S.2008FGB, FGA, FGG
2Pathology teach and tell: fibrinogen storage disease in a child with hypofibrinogenemia and decreased ceruloplasmin. (17701692)Bruzzi C.... Ahmed A.A.2007CP
3Fibrinogen Columbus: a novel gamma Gly200Val mutation causing hypofibrinogenemia in a family with associated thrombophilia. (17650452)Davis R.L.... Brennan S.O.2007FGG
4Analysis of hypofibrinogenemias found on routine coagulation screening tests and identification of heterozygous dysfibrinogenemia or fibrinogen deficiency (18154029)Hirota-Kawadobora M.... Katsuyama T.2007ALB
5Fibrinogen angers with a new deletion (gamma GVYYQ 346-350) causes hypofibrinogenemia with hepatic storage. (17883696)Dib N.... Cales P.2007FGG
6Clinical and biological features of 3 cases of hypofibrinogenemia associated with three different mutations (gamma Ala341Thr, Bbeta Tyr326Cys and Aalpha Asp496Asn). (17849064)Hanss M.... de Mazancourt P.2007FGB, FGA, FGG
7Novel fibrinogen mutation (gamma 313 Ser-->Asn) associated with hypofibrinogenemia in two unrelated families. (16607083)Meyer M.... Brennan S.O.2006FGG
8Fibrinogen gamma375 arg-->trp mutation (fibrinogen aguadilla) causes hereditary hypofibrinogenemia, hepatic endoplasmic reticulum storage disease and cirrhosis. (16819336)Rubbia-Brandt L.... Spahr L.2006FGG
9Hypofibrinogenemia caused by a nonsense mutation in the fibrinogen Bbeta chain gene. (14629469)Mimuro J.... Sakata Y.2003FGB
10A family with von Willebrand disease and hypofibrinogenemia (2246818)Shinmyozu K.... Osame M.1990VWF

Expression for genes affiliated with Hypofibrinogenemia

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1BioGPS
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Expression patterns in normal tissues for genes affiliated with Hypofibrinogenemia

Pathways for genes affiliated with Hypofibrinogenemia

Sources:
41Thomson Reuters, 10EMD Millipore, 34PharmGKB, 38Reactome, 36QIAGEN, 37R&D Systems, 20KEGG
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Compounds for genes affiliated with Hypofibrinogenemia

Sources:
32Novoseek , 34PharmGKB, 9DrugBank, 18HMDB, 42Tocris Bioscience
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Compounds related to hypofibrinogenemia according to GeneDecks:

(show top 50)    (show all 162)
idCompoundScoreTop Affiliating Genes
1clopidogrel32 34 9 18 9 14.5SERPINC1
2hepaplastin32 10.3ALB
3aspartate32 9.9F2, APOA1
4integrilin32 9.9PLAT
5abciximab32 9 9 11.8F3, VWF, F2
6tranexamic acid32 9 9 11.7SERPINE1, PLAT, SERPINC1, VWF
7eaca32 9.7SERPINC1, SERPINF2, PLAT, SERPINE1
8argatroban32 9 9 11.6F3, F2, FGA, SERPINC1
911-dehydrothromboxane b232 9.6VWF, SERPINE1, FGA, F2
10sucralfate32 9 9 11.6FGG, FGB, FGA, ALB
11reviparin32 9.5PLAT, SERPINC1, F3
12spectrozyme32 9.5SERPINC1, F3, F2, PLAT
13fondaparinux32 9.5F2, F3, PLAT, SERPINC1
14certoparin32 9.5SERPINC1, F3, F2
15fibrinopeptide a32 9.5SERPINC1, SERPINF2, FGA, F2, PLAT
16batroxobin32 9.4SERPINE1, FGB, F2, FGA, PLAT
17hemochron32 9.4F2, F3, FGA
18ticlopidine32 9 9 11.4FGA, VWF, SERPINC1, PLAT, F3
19protamine sulfate32 9.4PLAT, F2, F3, SERPINC1
20ancrod32 9.4F2, PLAT, FGA, SERPINC1, SERPINE1
21bivalirudin32 9 9 11.3FGA, F3, F2, PLAT, SERPINC1
22dextran 7032 9.3F2, F3, PLAT, ALB
23tirofiban32 9 9 11.3VWF, SERPINC1, F3, F2, PLAT
24phenprocoumon32 34 9 9 12.2SERPINC1, F3, F2, ALB
25perindopril32 34 9 9 12.1SERPINE1, VWF, ALB, PLAT
26levonorgestrel32 9 9 11.1SERPINC1, F3, PLAT, APOA1, F2
27dipyridamole42 32 9 9 12.1FGA, SERPINE1, VWF, F3, F2
28ppack32 9.1SERPINC1, VWF, FGA, F3, F2, PLAT
29dermatan sulfate32 9.1PLAT, F2, VWF, SERPINC1, F3
30ristocetin32 9.1SERPINC1, VWF, SERPINF2, PLAT, F2, F3
31hydroxyethyl starch32 9.1ALB, F3, SERPINC1, VWF, F2
32epsilon aminocaproic acid32 9.0SERPINC1, SERPINE1, SERPINF2, PLAT, F2, F3
33desogestrel32 9 9 10.8CP, F2, APOA1, SERPINC1
34desmopressin32 42 9 9 11.8F3, SERPINE1, SERPINF2, SERPINC1, VWF, F2
35gestodene32 9 9 10.7SERPINC1, APOA1, F2, CP
36simvastatin32 34 42 9 18 9 13.7F2, VWF, F3, APOA1, PLAT, SERPINE1
37prostacyclin32 8.7F3, APOA1, FGA, SERPINE1, SERPINC1, VWF
38warfarin32 34 9 18 9 12.6ALB, PLAT, VWF, F3, FGA, F2
39aprotinin32 9 9 10.5FGA, PLAT, SERPINE1, SERPINF2, SERPINC1, VWF
40creatinine32 8.5VWF, SERPINC1, FGA, APOA1, CP, F3
41aspirin32 34 18 10.3APOA1, F3, F2, PLAT, FGA, SERPINE1
42hirudin32 8.3FGA, VWF, SERPINC1, SERPINF2, SERPINE1, FGB
43protamine32 8.2FGA, SERPINC1, SERPINE1, CP, F2, F3
44thyroxine32 18 9.0VWF, PLAT, SERPINF2, APOA1, CP, ALB
45kininogen32 7.8F3, ALB, F2, VWF, PLAT, APOA1
46heparin32 9 18 9 10.5SERPINE1, F3, FGB, CP, FGA, ALB
47homocysteine32 18 8.3F3, F2, ALB, PLAT, CP, APOA1
48cholesterol32 9 18 9 10.1PLAT, PRF1, VWF, ALB, FGA, SERPINE1
49serine32 6.4SERPINE1, VWF, SERPINC1, FGA, SERPINF2, FGB
50fibrinogen32 6.3APOA1, FGG, FGA, SERPINE1, SERPINF2, SERPINC1

GO Terms for genes affiliated with Hypofibrinogenemia

Sources:
12Gene Ontology
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Cellular components related to hypofibrinogenemia according to GeneDecks:

idNameGO IDScoreTop Affiliating Genes
1cell cortexGO:0059389.8FGG, FGB, FGA
2fibrinogen complexGO:0055779.6FGG, FGB, FGA, SERPINF2
3platelet alpha granuleGO:0310919.5FGG, FGB, FGA, VWF
4external side of plasma membraneGO:0098979.2VWF, FGA, FGG, FGB
5extracellular matrixGO:0310129.2PLAT, SERPINE1, VWF, F3
6platelet alpha granule lumenGO:0310938.6FGG, VWF, ALB, SERPINF2, SERPINE1, FGA
7extracellular spaceGO:0056156.3SERPINE1, FGA, FGB, FGG, APOA1, F3
8extracellular regionGO:0055765.7FGB, FGG, FGA, SERPINE1, SERPINF2, SERPINC1

Biological processes related to hypofibrinogenemia according to GeneDecks:

(show all 11)
idNameGO IDScoreTop Affiliating Genes
1negative regulation of plasminogen activationGO:01075710.0SERPINE1, SERPINF2
2protein polymerizationGO:0512589.9FGG, FGB, FGA
3negative regulation of proteolysisGO:0458619.8PLAT, F2
4response to calcium ionGO:0515929.8FGA, FGB, FGG
5positive regulation of blood coagulationGO:0301949.7SERPINE1, F2
6negative regulation of fibrinolysisGO:0519189.7SERPINE1, F2, SERPINF2
7blood vessel morphogenesisGO:0485149.6SERPINF2, PLAT
8fibrinolysisGO:0427309.4PLAT, F2, SERPINF2, SERPINE1
9platelet degranulationGO:0025768.2VWF, ALB, SERPINF2, SERPINE1, FGA, FGB
10platelet activationGO:0301687.8ALB, F2, APOA1, FGG, FGB, FGA
11blood coagulationGO:0075966.9FGA, SERPINF2, SERPINC1, VWF, FGB, FGG

Molecular functions related to hypofibrinogenemia according to GeneDecks:

(show all 7)
idNameGO IDScoreTop Affiliating Genes
1eukaryotic cell surface bindingGO:0434999.6SERPINF2, FGA, FGB, FGG
2serine-type endopeptidase inhibitor activityGO:0048679.6SERPINE1, SERPINF2, SERPINC1
3protein binding, bridgingGO:0306749.5FGB, FGA, FGG
4protease bindingGO:0020209.1VWF, SERPINC1, SERPINF2, SERPINE1, F3
5receptor bindingGO:0051029.0SERPINE1, FGA, FGB, FGG, F2
6chaperone bindingGO:0510878.7VWF, FGB, ALB, CP
7protein bindingGO:0055155.6VWF, PRF1, STX11, PLAT, ALB, F2

Sources for Hypofibrinogenemia

2CDC
11FMA
18HMDB
19ICD9CM
20KEGG
24MeSH
25MGI
27NCIt
28NDF-RT
31NINDS
32Novoseek
33OMIM
35PubMed
36QIAGEN
43UMLS