Hypoprothrombinemias

Disease • C0020640

Definition

Absence or reduced levels of prothrombin in the blood.

Synonyms

Hypoprothrombinemias • Hypoprothrombinemia • Factor II Deficiency • Deficiency, factor II • Deficiencies, Factor II • Factor II Deficiencies • Prothrombin Deficiency • Deficiency, prothrombin • Deficiencies, Prothrombin • Prothrombin Deficiencies • PROTHROMBIN DEFIC • DEFIC FACTOR II • FACTOR II DEFIC • Hypoprothrombinemias [Disease/Finding] • Deficiency of factor II [prothrombin]

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

F2 gene    Hemorrhagic Disorders    Blood Coagulation Disorders, Inherited    Coagulation Protein Disorders   

Related concepts

# Concept name Type Relation Support Score
1 Coagulation Protein Disorders Disease Known Explain 118.30791
2 Blood Coagulation Disorders, Inherited Disease Known Explain 90.20291
3 Hemorrhagic Disorders Disease Known Explain 86.17853
4 F2 gene Gene Known Explain 15.63339
5 Factor VII Deficiency Disease Inferred Explain 4.88516
6 Factor V Deficiency Disease Inferred Explain 4.86076
7 Factor X Deficiency Disease Inferred Explain 4.81982
8 Factor XI Deficiency Disease Inferred Explain 4.80453
9 Factor XII Deficiency Disease Inferred Explain 4.72514
10 Factor XIII Deficiency Disease Inferred Explain 4.49154
11 Hemophilia B Disease Inferred Explain 4.32556
12 Afibrinogenemia Disease Inferred Explain 4.27222
13 Hemophilia A Disease Inferred Explain 3.78786
14 von Willebrand Disease Disease Inferred Explain 3.24828
15 Activated Protein C Resistance Disease Inferred Explain 2.02850
16 Thrombasthenia Disease Inferred Explain 1.86829
17 Blood Coagulation Disorders Disease Inferred Explain 1.79644
18 Wiskott-Aldrich Syndrome Disease Inferred Explain 1.71342
19 Hermanski-Pudlak Syndrome Disease Inferred Explain 1.70252
20 Bernard-Soulier Syndrome Disease Inferred Explain 1.44935
21 Platelet Storage Pool Deficiency Disease Inferred Explain 1.27838
22 Disseminated Intravascular Coagulation Disease Inferred Explain 1.04465
23 Blood Platelet Disorders Disease Inferred Explain 1.01523
24 Thrombocythemia, Essential Disease Inferred Explain 0.93169
25 Vitamin K Deficiency Disease Inferred Explain 0.89462
26 Waterhouse-Friderichsen Syndrome Disease Inferred Explain 0.77044
27 Purpura, Thrombocytopenic, Idiopathic Disease Inferred Explain 0.67996
28 F7 gene Gene Inferred Explain 0.52213
29 Thrombophilia Disease Inferred Explain 0.46137
30 Gray Platelet Syndrome Disease Inferred Explain 0.42089
31 Hematological Disease Disease Inferred Explain 0.37313
32 Vascular Hemostatic Disorders Disease Inferred Explain 0.34643
33 Antithrombin III Deficiency Disease Inferred Explain 0.33455
34 Protein C Deficiency Disease Inferred Explain 0.31778
35 F9 gene Gene Inferred Explain 0.28162
36 F11 gene Gene Inferred Explain 0.27236
37 F13B gene Gene Inferred Explain 0.25346
38 Hereditary factor I deficiency disease Disease Inferred Explain 0.23945
39 F5 gene Gene Inferred Explain 0.20067
40 Genetic Diseases, X-Linked Disease Inferred Explain 0.18312
41 F13A1 gene Gene Inferred Explain 0.14785
42 FGA gene Gene Inferred Explain 0.14477
43 F12 gene Gene Inferred Explain 0.14257
44 F10 gene Gene Inferred Explain 0.13600
45 FGB gene Gene Inferred Explain 0.12200
46 CFI gene Gene Inferred Explain 0.10608
47 Lymphopenia Disease Inferred Explain 0.10289
48 PROC gene Gene Inferred Explain 0.08489
49 Thrombocytosis Disease Inferred Explain 0.07709
50 Malnutrition Disease Inferred Explain 0.07264
51 GIANT PLATELET SYNDROME WITH THROMBOCYTOPENIA Disease Inferred Explain 0.07023
52 GP1BA gene Gene Inferred Explain 0.05864
53 Blood Protein Disorders Disease Inferred Explain 0.05748
54 P2RX1 gene Gene Inferred Explain 0.05723
55 Purpura Disease Inferred Explain 0.05721
56 Blood Platelets Other Inferred Explain 0.05190
57 HEMOPHILIA A WITH VASCULAR ABNORMALITY Disease Inferred Explain 0.04743
58 GP9 gene Gene Inferred Explain 0.04642
59 Protein S Deficiency Disease Inferred Explain 0.04448
60 VWF gene Gene Inferred Explain 0.04303
61 Genetic Diseases, Inborn Disease Inferred Explain 0.04238
62 Immunologic Deficiency Syndromes Disease Inferred Explain 0.04155
63 MTHFR gene Gene Inferred Explain 0.04132
64 propylene dichloride Compound Inferred Explain 0.04081
65 ITGA2B gene Gene Inferred Explain 0.04068
66 GP1BB gene Gene Inferred Explain 0.03660
67 Von Willebrand disease, platelet type Disease Inferred Explain 0.03597
68 von Willebrand Disease, Type 3 Disease Inferred Explain 0.03590
69 VON WILLEBRAND DISEASE, X-LINKED FORM Disease Inferred Explain 0.03590
70 F8 gene Gene Inferred Explain 0.03392
71 von Willebrand Disease, Recessive Form Disease Inferred Explain 0.03347
72 Warfarin Compound Inferred Explain 0.02718
73 Thrombocytopenia Disease Inferred Explain 0.02587
74 Avitaminosis Disease Inferred Explain 0.02375
75 Vitamin K Deficiency Bleeding Disease Inferred Explain 0.02243
76 THPO gene Gene Inferred Explain 0.02171
77 Thrombosis Disease Inferred Explain 0.02117
78 Thrombocytopenic purpura Disease Inferred Explain 0.02065
79 GGCX gene Gene Inferred Explain 0.02008
80 MPL gene Gene Inferred Explain 0.02005
81 Gestodene Compound Inferred Explain 0.01775
82 WAS gene Gene Inferred Explain 0.01713
83 blood coagulation, intrinsic pathway Function Inferred Explain 0.01704
84 Meningococcal meningitis Disease Inferred Explain 0.01666
85 Ethionine Compound Inferred Explain 0.01573
86 Ecchymosis Disease Inferred Explain 0.01370
87 ITGB3 gene Gene Inferred Explain 0.01342
88 SERPINC1 gene Gene Inferred Explain 0.01252
89 Benzbromarone Compound Inferred Explain 0.01241
90 Complement and coagulation cascades - Homo sapiens (human) Pathway Inferred Explain 0.01192
91 Propylthiouracil Compound Inferred Explain 0.01173
92 Adrenal gland hypofunction Disease Inferred Explain 0.01099
93 MIR223 gene Gene Inferred Explain 0.01076
94 PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY Disease Inferred Explain 0.01034
95 Autoimmune reaction Disease Inferred Explain 0.01028
96 Clofibrate Compound Inferred Explain 0.00940
97 Embolism and Thrombosis Disease Inferred Explain 0.00920
98 STORMORKEN SYNDROME Disease Inferred Explain 0.00903
99 estradiol valerate-dienogest Compound Inferred Explain 0.00900
100 peptidyl-glutamic acid carboxylation Function Inferred Explain 0.00864