Afibrinogenemia

Disease • C0001733

Definition

A usually inherited blood coagulation disorder characterized by the lack of fibrinogen in the blood, resulting in bleeding.

Synonyms

Afibrinogenemia • Afibrinogenemias • Fibrinogen Deficiency • Deficiency, fibrinogen • Deficiencies, Fibrinogen • Fibrinogen Deficiencies • FACTOR I DEFICIENCY, COMPLETE • Factor I Deficiency • DEFICIENCY FACTOR I • Deficiency, factor I • COMPLEMENT COMPONENT 3 INACTIVATOR DEFICIENCY • DEFIC FIBRINOGEN • FIBRINOGEN DEFIC • C3 INACTIVATOR DEFICIENCY • COMPLEMENT FACTOR I DEFICIENCY • Afibrinogenemia [Disease/Finding] • Deficiency of factor I [fibrinogen]

Linked items?Related concepts, ordered by their global importance in the network.

FGA gene    FGB gene    Hemorrhagic Disorders    Blood Coagulation Disorders, Inherited    CFI gene    Coagulation Protein Disorders    Hereditary factor I deficiency disease   

Related concepts

# Concept name Type Relation Support Score
1 Hereditary factor I deficiency disease Disease Known Explain 86.04234
2 Coagulation Protein Disorders Disease Known Explain 41.15889
3 FGB gene Gene Known Explain 37.67253
4 CFI gene Gene Known Explain 37.54695
5 Blood Coagulation Disorders, Inherited Disease Known Explain 30.71899
6 FGA gene Gene Known Explain 28.32322
7 Hemorrhagic Disorders Disease Known Explain 27.86478
8 Factor VII Deficiency Disease Inferred Explain 1.20608
9 Hypoprothrombinemias Disease Inferred Explain 1.20580
10 Factor V Deficiency Disease Inferred Explain 1.20033
11 Factor X Deficiency Disease Inferred Explain 1.19101
12 Factor XI Deficiency Disease Inferred Explain 1.18556
13 Factor XII Deficiency Disease Inferred Explain 1.16721
14 Factor XIII Deficiency Disease Inferred Explain 1.12194
15 Hemophilia B Disease Inferred Explain 1.06773
16 Hemophilia A Disease Inferred Explain 0.94147
17 von Willebrand Disease Disease Inferred Explain 0.82141
18 Activated Protein C Resistance Disease Inferred Explain 0.75500
19 Blood Coagulation Disorders Disease Inferred Explain 0.53059
20 Thrombasthenia Disease Inferred Explain 0.34997
21 Wiskott-Aldrich Syndrome Disease Inferred Explain 0.31771
22 Hermanski-Pudlak Syndrome Disease Inferred Explain 0.29800
23 Bernard-Soulier Syndrome Disease Inferred Explain 0.27476
24 Blood Platelet Disorders Disease Inferred Explain 0.22600
25 Platelet Storage Pool Deficiency Disease Inferred Explain 0.17654
26 Gray Platelet Syndrome Disease Inferred Explain 0.14691
27 Disseminated Intravascular Coagulation Disease Inferred Explain 0.14334
28 Thrombophilia Disease Inferred Explain 0.13626
29 F7 gene Gene Inferred Explain 0.12482
30 Antithrombin III Deficiency Disease Inferred Explain 0.12305
31 Thrombocythemia, Essential Disease Inferred Explain 0.12096
32 Protein C Deficiency Disease Inferred Explain 0.11537
33 Vitamin K Deficiency Disease Inferred Explain 0.11471
34 Waterhouse-Friderichsen Syndrome Disease Inferred Explain 0.08677
35 FGG gene Gene Inferred Explain 0.08343
36 Purpura, Thrombocytopenic, Idiopathic Disease Inferred Explain 0.07612
37 F13B gene Gene Inferred Explain 0.07449
38 estradiol valerate-dienogest Compound Inferred Explain 0.06858
39 Complement and coagulation cascades - Homo sapiens (human) Pathway Inferred Explain 0.06849
40 F9 gene Gene Inferred Explain 0.06625
41 F13A1 gene Gene Inferred Explain 0.06590
42 F11 gene Gene Inferred Explain 0.06554
43 Hematological Disease Disease Inferred Explain 0.05729
44 F5 gene Gene Inferred Explain 0.05543
45 platelet alpha granule Component Inferred Explain 0.05473
46 fibrinogen complex location Component Inferred Explain 0.05457
47 dienogest Compound Inferred Explain 0.05404
48 Gestodene Compound Inferred Explain 0.05234
49 Desogestrel Compound Inferred Explain 0.04646
50 Norethindrone Compound Inferred Explain 0.04602
51 F2 gene Gene Inferred Explain 0.04530
52 Mercilon Compound Inferred Explain 0.04418
53 Genetic Diseases, X-Linked Disease Inferred Explain 0.04412
54 norgestimate Compound Inferred Explain 0.04361
55 F10 gene Gene Inferred Explain 0.04194
56 Vascular Hemostatic Disorders Disease Inferred Explain 0.04026
57 Hemolytic-Uremic Syndrome Disease Inferred Explain 0.03951
58 eukaryotic cell surface binding Function Inferred Explain 0.03816
59 F12 gene Gene Inferred Explain 0.03785
60 PROC gene Gene Inferred Explain 0.03417
61 SERPINA5 gene Gene Inferred Explain 0.02967
62 Levonorgestrel Compound Inferred Explain 0.02850
63 CFH gene Gene Inferred Explain 0.02833
64 platelet alpha granule lumen Component Inferred Explain 0.02608
65 MIS12 gene Gene Inferred Explain 0.02240
66 P2RX1 gene Gene Inferred Explain 0.02170
67 protein polymerization Function Inferred Explain 0.02167
68 Blood Protein Disorders Disease Inferred Explain 0.02075
69 complement activation, classical pathway Function Inferred Explain 0.02045
70 Lymphopenia Disease Inferred Explain 0.02001
71 KLK6 gene Gene Inferred Explain 0.01939
72 VWF gene Gene Inferred Explain 0.01859
73 KEGG:hsa05150 Pathway Inferred Explain 0.01852
74 platelet degranulation Function Inferred Explain 0.01840
75 ITGA2B gene Gene Inferred Explain 0.01834
76 NID1 gene Gene Inferred Explain 0.01823
77 KHDRBS2 gene Gene Inferred Explain 0.01770
78 protein binding, bridging Function Inferred Explain 0.01729
79 response to calcium ion Function Inferred Explain 0.01686
80 Genetic Diseases, Inborn Disease Inferred Explain 0.01565
81 Protein S Deficiency Disease Inferred Explain 0.01523
82 Malnutrition Disease Inferred Explain 0.01516
83 MTHFR gene Gene Inferred Explain 0.01475
84 C3 gene Gene Inferred Explain 0.01457
85 SERPINC1 gene Gene Inferred Explain 0.01457
86 scavenger receptor activity Function Inferred Explain 0.01392
87 GIANT PLATELET SYNDROME WITH THROMBOCYTOPENIA Disease Inferred Explain 0.01384
88 F8 gene Gene Inferred Explain 0.01347
89 HEMOPHILIA A WITH VASCULAR ABNORMALITY Disease Inferred Explain 0.01312
90 Amyloidosis, familial visceral Disease Inferred Explain 0.01246
91 Thrombocytosis Disease Inferred Explain 0.01225
92 PLAT gene Gene Inferred Explain 0.01216
93 Purpura Disease Inferred Explain 0.01186
94 PROS1 gene Gene Inferred Explain 0.01065
95 Blood Platelets Other Inferred Explain 0.01026
96 von Willebrand Disease, Type 3 Disease Inferred Explain 0.01019
97 VON WILLEBRAND DISEASE, X-LINKED FORM Disease Inferred Explain 0.01019
98 GP1BA gene Gene Inferred Explain 0.01018
99 Ethinyl Estradiol Compound Inferred Explain 0.01005
100 Von Willebrand disease, platelet type Disease Inferred Explain 0.00999