|
Coagulation Protein Disorders
Related concepts
|
#
|
Concept name
|
Type
|
Relation
|
Support
|
Score
|
|
1
|
Blood Coagulation Disorders, Inherited
|
Disease
|
Inferred
|
Explain
|
60.43337
|
|
2
|
Hemorrhagic Disorders
|
Disease
|
Inferred
|
Explain
|
50.56026
|
|
3
|
Hypoprothrombinemias
|
Disease
|
Known
|
Explain
|
28.14246
|
|
4
|
Factor VII Deficiency
|
Disease
|
Known
|
Explain
|
28.02497
|
|
5
|
Factor V Deficiency
|
Disease
|
Known
|
Explain
|
28.00246
|
|
6
|
Factor X Deficiency
|
Disease
|
Known
|
Explain
|
27.79016
|
|
7
|
Factor XI Deficiency
|
Disease
|
Known
|
Explain
|
27.63523
|
|
8
|
Factor XII Deficiency
|
Disease
|
Known
|
Explain
|
27.25246
|
|
9
|
Activated Protein C Resistance
|
Disease
|
Known
|
Explain
|
26.74934
|
|
10
|
Factor XIII Deficiency
|
Disease
|
Known
|
Explain
|
25.83663
|
|
11
|
Hemophilia B
|
Disease
|
Known
|
Explain
|
24.72205
|
|
12
|
Afibrinogenemia
|
Disease
|
Known
|
Explain
|
24.46825
|
|
13
|
Hemophilia A
|
Disease
|
Known
|
Explain
|
21.65193
|
|
14
|
von Willebrand Disease
|
Disease
|
Known
|
Explain
|
17.69289
|
|
15
|
Blood Coagulation Disorders
|
Disease
|
Known
|
Explain
|
9.83496
|
|
16
|
F13B gene
|
Gene
|
Inferred
|
Explain
|
1.39880
|
|
17
|
Hereditary factor I deficiency disease
|
Disease
|
Inferred
|
Explain
|
1.32547
|
|
18
|
F9 gene
|
Gene
|
Inferred
|
Explain
|
1.26021
|
|
19
|
F11 gene
|
Gene
|
Inferred
|
Explain
|
1.24740
|
|
20
|
Thrombophilia
|
Disease
|
Inferred
|
Explain
|
1.01802
|
|
21
|
F5 gene
|
Gene
|
Inferred
|
Explain
|
0.92890
|
|
22
|
F7 gene
|
Gene
|
Inferred
|
Explain
|
0.88347
|
|
23
|
Blood Platelet Disorders
|
Disease
|
Inferred
|
Explain
|
0.75696
|
|
24
|
F12 gene
|
Gene
|
Inferred
|
Explain
|
0.74294
|
|
25
|
Thrombasthenia
|
Disease
|
Inferred
|
Explain
|
0.72415
|
|
26
|
F13A1 gene
|
Gene
|
Inferred
|
Explain
|
0.68665
|
|
27
|
Hermanski-Pudlak Syndrome
|
Disease
|
Inferred
|
Explain
|
0.65762
|
|
28
|
Platelet Storage Pool Deficiency
|
Disease
|
Inferred
|
Explain
|
0.65187
|
|
29
|
Wiskott-Aldrich Syndrome
|
Disease
|
Inferred
|
Explain
|
0.64750
|
|
30
|
FGA gene
|
Gene
|
Inferred
|
Explain
|
0.64466
|
|
31
|
F10 gene
|
Gene
|
Inferred
|
Explain
|
0.61155
|
|
32
|
FGB gene
|
Gene
|
Inferred
|
Explain
|
0.60157
|
|
33
|
Disseminated Intravascular Coagulation
|
Disease
|
Inferred
|
Explain
|
0.59600
|
|
34
|
CFI gene
|
Gene
|
Inferred
|
Explain
|
0.58303
|
|
35
|
Bernard-Soulier Syndrome
|
Disease
|
Inferred
|
Explain
|
0.56140
|
|
36
|
Genetic Diseases, X-Linked
|
Disease
|
Inferred
|
Explain
|
0.53611
|
|
37
|
Thrombocythemia, Essential
|
Disease
|
Inferred
|
Explain
|
0.45114
|
|
38
|
F2 gene
|
Gene
|
Inferred
|
Explain
|
0.44467
|
|
39
|
Vitamin K Deficiency
|
Disease
|
Inferred
|
Explain
|
0.43313
|
|
40
|
Gray Platelet Syndrome
|
Disease
|
Inferred
|
Explain
|
0.30612
|
|
41
|
Antithrombin III Deficiency
|
Disease
|
Inferred
|
Explain
|
0.29186
|
|
42
|
Protein C Deficiency
|
Disease
|
Inferred
|
Explain
|
0.27695
|
|
43
|
HEMOPHILIA A WITH VASCULAR ABNORMALITY
|
Disease
|
Inferred
|
Explain
|
0.24836
|
|
44
|
Hematological Disease
|
Disease
|
Inferred
|
Explain
|
0.22734
|
|
45
|
Waterhouse-Friderichsen Syndrome
|
Disease
|
Inferred
|
Explain
|
0.18938
|
|
46
|
VWF gene
|
Gene
|
Inferred
|
Explain
|
0.18397
|
|
47
|
Protein S Deficiency
|
Disease
|
Inferred
|
Explain
|
0.18271
|
|
48
|
von Willebrand Disease, Type 3
|
Disease
|
Inferred
|
Explain
|
0.18265
|
|
49
|
VON WILLEBRAND DISEASE, X-LINKED FORM
|
Disease
|
Inferred
|
Explain
|
0.18265
|
|
50
|
Von Willebrand disease, platelet type
|
Disease
|
Inferred
|
Explain
|
0.17326
|
|
51
|
von Willebrand Disease, Recessive Form
|
Disease
|
Inferred
|
Explain
|
0.16758
|
|
52
|
Purpura, Thrombocytopenic, Idiopathic
|
Disease
|
Inferred
|
Explain
|
0.15682
|
|
53
|
Ethionine
|
Compound
|
Inferred
|
Explain
|
0.10456
|
|
54
|
F8 gene
|
Gene
|
Inferred
|
Explain
|
0.10135
|
|
55
|
Purpura
|
Disease
|
Inferred
|
Explain
|
0.08658
|
|
56
|
Ecchymosis
|
Disease
|
Inferred
|
Explain
|
0.08519
|
|
57
|
Vascular Hemostatic Disorders
|
Disease
|
Inferred
|
Explain
|
0.08312
|
|
58
|
Benzbromarone
|
Compound
|
Inferred
|
Explain
|
0.08227
|
|
59
|
Propylthiouracil
|
Compound
|
Inferred
|
Explain
|
0.07701
|
|
60
|
Blood Protein Disorders
|
Disease
|
Inferred
|
Explain
|
0.07409
|
|
61
|
PROC gene
|
Gene
|
Inferred
|
Explain
|
0.06639
|
|
62
|
Clofibrate
|
Compound
|
Inferred
|
Explain
|
0.06201
|
|
63
|
GGCX gene
|
Gene
|
Inferred
|
Explain
|
0.05328
|
|
64
|
GP1BA gene
|
Gene
|
Inferred
|
Explain
|
0.04823
|
|
65
|
P2RX1 gene
|
Gene
|
Inferred
|
Explain
|
0.03890
|
|
66
|
Thrombocytosis
|
Disease
|
Inferred
|
Explain
|
0.03836
|
|
67
|
Lymphopenia
|
Disease
|
Inferred
|
Explain
|
0.03795
|
|
68
|
Omeprazole
|
Compound
|
Inferred
|
Explain
|
0.03734
|
|
69
|
MTHFR gene
|
Gene
|
Inferred
|
Explain
|
0.03265
|
|
70
|
Genetic Diseases, Inborn
|
Disease
|
Inferred
|
Explain
|
0.03096
|
|
71
|
Malnutrition
|
Disease
|
Inferred
|
Explain
|
0.02889
|
|
72
|
VKORC1 gene
|
Gene
|
Inferred
|
Explain
|
0.02836
|
|
73
|
GIANT PLATELET SYNDROME WITH THROMBOCYTOPENIA
|
Disease
|
Inferred
|
Explain
|
0.02671
|
|
74
|
Warfarin
|
Compound
|
Inferred
|
Explain
|
0.02417
|
|
75
|
propylene dichloride
|
Compound
|
Inferred
|
Explain
|
0.02287
|
|
76
|
Gestodene
|
Compound
|
Inferred
|
Explain
|
0.02145
|
|
77
|
Complement and coagulation cascades - Homo sapiens (human)
|
Pathway
|
Inferred
|
Explain
|
0.02131
|
|
78
|
Blood Platelets
|
Other
|
Inferred
|
Explain
|
0.01954
|
|
79
|
GP9 gene
|
Gene
|
Inferred
|
Explain
|
0.01916
|
|
80
|
Mercilon
|
Compound
|
Inferred
|
Explain
|
0.01723
|
|
81
|
blood coagulation, intrinsic pathway
|
Function
|
Inferred
|
Explain
|
0.01687
|
|
82
|
Immunologic Deficiency Syndromes
|
Disease
|
Inferred
|
Explain
|
0.01636
|
|
83
|
Thioacetamide
|
Compound
|
Inferred
|
Explain
|
0.01628
|
|
84
|
Purpura, Thrombotic Thrombocytopenic
|
Disease
|
Inferred
|
Explain
|
0.01600
|
|
85
|
GP1BB gene
|
Gene
|
Inferred
|
Explain
|
0.01467
|
|
86
|
ITGA2B gene
|
Gene
|
Inferred
|
Explain
|
0.01435
|
|
87
|
Amino Acids, Sulfur
|
Compound
|
Inferred
|
Explain
|
0.01432
|
|
88
|
Skin Manifestations
|
Disease
|
Inferred
|
Explain
|
0.01399
|
|
89
|
Cyclophosphamide
|
Compound
|
Inferred
|
Explain
|
0.01393
|
|
90
|
Thrombocytopenia
|
Disease
|
Inferred
|
Explain
|
0.01239
|
|
91
|
Thrombocytopenic purpura
|
Disease
|
Inferred
|
Explain
|
0.01163
|
|
92
|
Thrombosis
|
Disease
|
Inferred
|
Explain
|
0.01045
|
|
93
|
Vitamin K Deficiency Bleeding
|
Disease
|
Inferred
|
Explain
|
0.01004
|
|
94
|
PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY
|
Disease
|
Inferred
|
Explain
|
0.00980
|
|
95
|
Avitaminosis
|
Disease
|
Inferred
|
Explain
|
0.00977
|
|
96
|
FGG gene
|
Gene
|
Inferred
|
Explain
|
0.00921
|
|
97
|
STORMORKEN SYNDROME
|
Disease
|
Inferred
|
Explain
|
0.00858
|
|
98
|
VWF wt Allele
|
Gene
|
Inferred
|
Explain
|
0.00838
|
|
99
|
SERPINC1 gene
|
Gene
|
Inferred
|
Explain
|
0.00763
|
|
100
|
blood coagulation, extrinsic pathway
|
Function
|
Inferred
|
Explain
|
0.00756
|
|