Factor XI Deficiency

Disease • C0015523

Definition

A rare inherited bleeding disorder caused by deficiency of coagulation factor XI. It may be asymptomatic or manifest with bleeding.

Synonyms

Factor XI Deficiency • Deficiencies, Factor XI • Factor XI Deficiencies • Deficiency, Factor XI • Congenital factor XI deficiency • Hemophilia C • Deficiency, PTA • PTA deficiency • Plasma Thromboplastin Antecedent Deficiency • Rosenthal Syndrome • Rosenthal Syndromes • Rosenthal's Syndrome • Rosenthal's Syndromes • Rosenthals Syndrome • Syndrome, Rosenthal's • Syndrome, Rosenthal • Rosenthal's disease • Hereditary factor XI deficiency • Plasma thromboplastin antecedent [PTA] deficiency • DEFIC FACTOR XI • FACTOR XI DEFIC • F11 deficiency • Cong factor xi disorder • Factor XI Deficiency [Disease/Finding]

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

F11 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 122.03854
2 Blood Coagulation Disorders, Inherited Disease Known Explain 91.37811
3 F11 gene Gene Known Explain 83.17123
4 Hemorrhagic Disorders Disease Known Explain 82.84833
5 Hypoprothrombinemias Disease Inferred Explain 3.69547
6 Factor VII Deficiency Disease Inferred Explain 3.68939
7 Factor V Deficiency Disease Inferred Explain 3.67503
8 Factor X Deficiency Disease Inferred Explain 3.64743
9 Factor XII Deficiency Disease Inferred Explain 3.58251
10 Factor XIII Deficiency Disease Inferred Explain 3.40330
11 Hemophilia B Disease Inferred Explain 3.27417
12 Afibrinogenemia Disease Inferred Explain 3.26461
13 Hemophilia A Disease Inferred Explain 2.87660
14 von Willebrand Disease Disease Inferred Explain 2.53009
15 Activated Protein C Resistance Disease Inferred Explain 2.30495
16 Blood Coagulation Disorders Disease Inferred Explain 1.38812
17 Thrombasthenia Disease Inferred Explain 1.07177
18 Wiskott-Aldrich Syndrome Disease Inferred Explain 0.97815
19 Hermanski-Pudlak Syndrome Disease Inferred Explain 0.91447
20 Bernard-Soulier Syndrome Disease Inferred Explain 0.85777
21 Blood Platelet Disorders Disease Inferred Explain 0.70605
22 Platelet Storage Pool Deficiency Disease Inferred Explain 0.53351
23 Gray Platelet Syndrome Disease Inferred Explain 0.45338
24 Disseminated Intravascular Coagulation Disease Inferred Explain 0.42307
25 Thrombophilia Disease Inferred Explain 0.37268
26 Antithrombin III Deficiency Disease Inferred Explain 0.36905
27 Thrombocythemia, Essential Disease Inferred Explain 0.36274
28 Protein C Deficiency Disease Inferred Explain 0.34766
29 Vitamin K Deficiency Disease Inferred Explain 0.34413
30 F7 gene Gene Inferred Explain 0.27009
31 Waterhouse-Friderichsen Syndrome Disease Inferred Explain 0.26522
32 Purpura, Thrombocytopenic, Idiopathic Disease Inferred Explain 0.23135
33 F13B gene Gene Inferred Explain 0.20350
34 F9 gene Gene Inferred Explain 0.20226
35 Hereditary factor I deficiency disease Disease Inferred Explain 0.19197
36 Hematological Disease Disease Inferred Explain 0.17200
37 F5 gene Gene Inferred Explain 0.14015
38 Genetic Diseases, X-Linked Disease Inferred Explain 0.13774
39 F12 gene Gene Inferred Explain 0.13157
40 F2 gene Gene Inferred Explain 0.12795
41 Vascular Hemostatic Disorders Disease Inferred Explain 0.12444
42 GP1BA gene Gene Inferred Explain 0.11855
43 F13A1 gene Gene Inferred Explain 0.10471
44 FGA gene Gene Inferred Explain 0.10430
45 plasminogen activation Function Inferred Explain 0.10322
46 F10 gene Gene Inferred Explain 0.10262
47 FGB gene Gene Inferred Explain 0.09642
48 CFI gene Gene Inferred Explain 0.08692
49 positive regulation of fibrinolysis Function Inferred Explain 0.08485
50 blood coagulation, intrinsic pathway Function Inferred Explain 0.08243
51 P2RX1 gene Gene Inferred Explain 0.06508
52 Lymphopenia Disease Inferred Explain 0.06237
53 Blood Protein Disorders Disease Inferred Explain 0.06185
54 regulation of blood coagulation Function Inferred Explain 0.06172
55 Genetic Diseases, Inborn Disease Inferred Explain 0.04796
56 Malnutrition Disease Inferred Explain 0.04755
57 PROC gene Gene Inferred Explain 0.04701
58 GIANT PLATELET SYNDROME WITH THROMBOCYTOPENIA Disease Inferred Explain 0.04367
59 MTHFR gene Gene Inferred Explain 0.04323
60 Protein S Deficiency Disease Inferred Explain 0.04186
61 HEMOPHILIA A WITH VASCULAR ABNORMALITY Disease Inferred Explain 0.04019
62 VWF gene Gene Inferred Explain 0.04009
63 Thrombocytosis Disease Inferred Explain 0.03832
64 SERPINF2 gene Gene Inferred Explain 0.03801
65 Complement and coagulation cascades - Homo sapiens (human) Pathway Inferred Explain 0.03735
66 SERPINA5 gene Gene Inferred Explain 0.03518
67 Purpura Disease Inferred Explain 0.03327
68 Von Willebrand disease, platelet type Disease Inferred Explain 0.03285
69 Blood Platelets Other Inferred Explain 0.03249
70 GP9 gene Gene Inferred Explain 0.03217
71 von Willebrand Disease, Type 3 Disease Inferred Explain 0.03174
72 VON WILLEBRAND DISEASE, X-LINKED FORM Disease Inferred Explain 0.03174
73 TFPI2 gene Gene Inferred Explain 0.03138
74 von Willebrand Disease, Recessive Form Disease Inferred Explain 0.03040
75 Immunologic Deficiency Syndromes Disease Inferred Explain 0.02738
76 GP1BB gene Gene Inferred Explain 0.02466
77 KNG1 gene Gene Inferred Explain 0.02181
78 F8 gene Gene Inferred Explain 0.02165
79 ITGA2B gene Gene Inferred Explain 0.01948
80 propylene dichloride Compound Inferred Explain 0.01793
81 Warfarin Compound Inferred Explain 0.01615
82 Thrombocytopenia Disease Inferred Explain 0.01577
83 HGF gene Gene Inferred Explain 0.01520
84 Ethionine Compound Inferred Explain 0.01399
85 Blood coagulation Function Inferred Explain 0.01234
86 Ecchymosis Disease Inferred Explain 0.01197
87 Heparin Binding Function Inferred Explain 0.01155
88 Avitaminosis Disease Inferred Explain 0.01133
89 Benzbromarone Compound Inferred Explain 0.01105
90 Thrombocytopenic purpura Disease Inferred Explain 0.01074
91 WAS gene Gene Inferred Explain 0.01065
92 Propylthiouracil Compound Inferred Explain 0.01061
93 Vitamin K Deficiency Bleeding Disease Inferred Explain 0.01023
94 GGCX gene Gene Inferred Explain 0.00959
95 KLKB1 gene Gene Inferred Explain 0.00932
96 serine-type endopeptidase activity Function Inferred Explain 0.00918
97 THPO gene Gene Inferred Explain 0.00852
98 ITGB3 gene Gene Inferred Explain 0.00841
99 Clofibrate Compound Inferred Explain 0.00835
100 PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY Disease Inferred Explain 0.00807