|
Blood Coagulation Disorders, Inherited
Related concepts
|
#
|
Concept name
|
Type
|
Relation
|
Support
|
Score
|
|
1
|
Coagulation Protein Disorders
|
Disease
|
Inferred
|
Explain
|
34.69288
|
|
2
|
Hemorrhagic Disorders
|
Disease
|
Inferred
|
Explain
|
26.27454
|
|
3
|
Hypoprothrombinemias
|
Disease
|
Known
|
Explain
|
10.78985
|
|
4
|
Factor VII Deficiency
|
Disease
|
Known
|
Explain
|
10.74407
|
|
5
|
Factor V Deficiency
|
Disease
|
Known
|
Explain
|
10.73438
|
|
6
|
Factor X Deficiency
|
Disease
|
Known
|
Explain
|
10.65208
|
|
7
|
Activated Protein C Resistance
|
Disease
|
Known
|
Explain
|
10.61227
|
|
8
|
Factor XI Deficiency
|
Disease
|
Known
|
Explain
|
10.59423
|
|
9
|
Factor XII Deficiency
|
Disease
|
Known
|
Explain
|
10.44611
|
|
10
|
Factor XIII Deficiency
|
Disease
|
Known
|
Explain
|
9.90193
|
|
11
|
Hemophilia B
|
Disease
|
Known
|
Explain
|
9.55177
|
|
12
|
Afibrinogenemia
|
Disease
|
Known
|
Explain
|
9.37758
|
|
13
|
Gray Platelet Syndrome
|
Disease
|
Known
|
Explain
|
8.82995
|
|
14
|
Hemophilia A
|
Disease
|
Known
|
Explain
|
8.30163
|
|
15
|
Thrombasthenia
|
Disease
|
Known
|
Explain
|
7.42931
|
|
16
|
von Willebrand Disease
|
Disease
|
Known
|
Explain
|
7.24492
|
|
17
|
Antithrombin III Deficiency
|
Disease
|
Known
|
Explain
|
7.23958
|
|
18
|
Wiskott-Aldrich Syndrome
|
Disease
|
Known
|
Explain
|
6.78689
|
|
19
|
Protein C Deficiency
|
Disease
|
Known
|
Explain
|
6.74938
|
|
20
|
Bernard-Soulier Syndrome
|
Disease
|
Known
|
Explain
|
5.67937
|
|
21
|
Hermanski-Pudlak Syndrome
|
Disease
|
Known
|
Explain
|
4.99006
|
|
22
|
Blood Platelet Disorders
|
Disease
|
Inferred
|
Explain
|
4.50741
|
|
23
|
Blood Coagulation Disorders
|
Disease
|
Known
|
Explain
|
4.06386
|
|
24
|
Thrombophilia
|
Disease
|
Inferred
|
Explain
|
2.69092
|
|
25
|
P2RX1 gene
|
Gene
|
Known
|
Explain
|
1.42042
|
|
26
|
Genetic Diseases, Inborn
|
Disease
|
Known
|
Explain
|
0.92200
|
|
27
|
MTHFR gene
|
Gene
|
Known
|
Explain
|
0.81450
|
|
28
|
Blood Protein Disorders
|
Disease
|
Inferred
|
Explain
|
0.74488
|
|
29
|
Platelet Storage Pool Deficiency
|
Disease
|
Inferred
|
Explain
|
0.55982
|
|
30
|
F13B gene
|
Gene
|
Inferred
|
Explain
|
0.53604
|
|
31
|
Hereditary factor I deficiency disease
|
Disease
|
Inferred
|
Explain
|
0.50755
|
|
32
|
Genetic Diseases, X-Linked
|
Disease
|
Inferred
|
Explain
|
0.50560
|
|
33
|
F9 gene
|
Gene
|
Inferred
|
Explain
|
0.49385
|
|
34
|
F11 gene
|
Gene
|
Inferred
|
Explain
|
0.48839
|
|
35
|
Lymphopenia
|
Disease
|
Inferred
|
Explain
|
0.39429
|
|
36
|
F7 gene
|
Gene
|
Inferred
|
Explain
|
0.37292
|
|
37
|
Disseminated Intravascular Coagulation
|
Disease
|
Inferred
|
Explain
|
0.37219
|
|
38
|
F5 gene
|
Gene
|
Inferred
|
Explain
|
0.37150
|
|
39
|
F12 gene
|
Gene
|
Inferred
|
Explain
|
0.29156
|
|
40
|
Malnutrition
|
Disease
|
Inferred
|
Explain
|
0.26894
|
|
41
|
GIANT PLATELET SYNDROME WITH THROMBOCYTOPENIA
|
Disease
|
Inferred
|
Explain
|
0.26604
|
|
42
|
F13A1 gene
|
Gene
|
Inferred
|
Explain
|
0.26438
|
|
43
|
FGA gene
|
Gene
|
Inferred
|
Explain
|
0.25877
|
|
44
|
F10 gene
|
Gene
|
Inferred
|
Explain
|
0.24535
|
|
45
|
FGB gene
|
Gene
|
Inferred
|
Explain
|
0.23809
|
|
46
|
Thrombocythemia, Essential
|
Disease
|
Inferred
|
Explain
|
0.23657
|
|
47
|
Hematological Disease
|
Disease
|
Inferred
|
Explain
|
0.23599
|
|
48
|
Protein S Deficiency
|
Disease
|
Inferred
|
Explain
|
0.22893
|
|
49
|
CFI gene
|
Gene
|
Inferred
|
Explain
|
0.22393
|
|
50
|
PROC gene
|
Gene
|
Inferred
|
Explain
|
0.22327
|
|
51
|
F2 gene
|
Gene
|
Inferred
|
Explain
|
0.21288
|
|
52
|
Vitamin K Deficiency
|
Disease
|
Inferred
|
Explain
|
0.19954
|
|
53
|
Blood Platelets
|
Other
|
Inferred
|
Explain
|
0.19750
|
|
54
|
Warfarin
|
Compound
|
Inferred
|
Explain
|
0.16624
|
|
55
|
GP9 gene
|
Gene
|
Inferred
|
Explain
|
0.16347
|
|
56
|
Immunologic Deficiency Syndromes
|
Disease
|
Inferred
|
Explain
|
0.15515
|
|
57
|
GP1BB gene
|
Gene
|
Inferred
|
Explain
|
0.12975
|
|
58
|
GP1BA gene
|
Gene
|
Inferred
|
Explain
|
0.12523
|
|
59
|
ITGA2B gene
|
Gene
|
Inferred
|
Explain
|
0.11186
|
|
60
|
HEMOPHILIA A WITH VASCULAR ABNORMALITY
|
Disease
|
Inferred
|
Explain
|
0.09504
|
|
61
|
Waterhouse-Friderichsen Syndrome
|
Disease
|
Inferred
|
Explain
|
0.09477
|
|
62
|
Purpura, Thrombocytopenic, Idiopathic
|
Disease
|
Inferred
|
Explain
|
0.08167
|
|
63
|
VWF gene
|
Gene
|
Inferred
|
Explain
|
0.08161
|
|
64
|
Thrombocytopenia
|
Disease
|
Inferred
|
Explain
|
0.07484
|
|
65
|
von Willebrand Disease, Type 3
|
Disease
|
Inferred
|
Explain
|
0.07455
|
|
66
|
VON WILLEBRAND DISEASE, X-LINKED FORM
|
Disease
|
Inferred
|
Explain
|
0.07455
|
|
67
|
Von Willebrand disease, platelet type
|
Disease
|
Inferred
|
Explain
|
0.07376
|
|
68
|
von Willebrand Disease, Recessive Form
|
Disease
|
Inferred
|
Explain
|
0.06845
|
|
69
|
WAS gene
|
Gene
|
Inferred
|
Explain
|
0.06341
|
|
70
|
Thrombocytosis
|
Disease
|
Inferred
|
Explain
|
0.06155
|
|
71
|
SERPINC1 gene
|
Gene
|
Inferred
|
Explain
|
0.05260
|
|
72
|
ITGB3 gene
|
Gene
|
Inferred
|
Explain
|
0.04596
|
|
73
|
Vascular Hemostatic Disorders
|
Disease
|
Inferred
|
Explain
|
0.04445
|
|
74
|
F8 gene
|
Gene
|
Inferred
|
Explain
|
0.04411
|
|
75
|
Ethionine
|
Compound
|
Inferred
|
Explain
|
0.04126
|
|
76
|
Purpura
|
Disease
|
Inferred
|
Explain
|
0.03952
|
|
77
|
PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY
|
Disease
|
Inferred
|
Explain
|
0.03782
|
|
78
|
Purpura, Thrombotic Thrombocytopenic
|
Disease
|
Inferred
|
Explain
|
0.03468
|
|
79
|
Ecchymosis
|
Disease
|
Inferred
|
Explain
|
0.03411
|
|
80
|
Benzbromarone
|
Compound
|
Inferred
|
Explain
|
0.03248
|
|
81
|
STORMORKEN SYNDROME
|
Disease
|
Inferred
|
Explain
|
0.03203
|
|
82
|
Propylthiouracil
|
Compound
|
Inferred
|
Explain
|
0.03046
|
|
83
|
Gestodene
|
Compound
|
Inferred
|
Explain
|
0.02731
|
|
84
|
Dysgammaglobulinemia
|
Disease
|
Inferred
|
Explain
|
0.02468
|
|
85
|
Clofibrate
|
Compound
|
Inferred
|
Explain
|
0.02454
|
|
86
|
GGCX gene
|
Gene
|
Inferred
|
Explain
|
0.02407
|
|
87
|
Hypergammaglobulinemia
|
Disease
|
Inferred
|
Explain
|
0.02349
|
|
88
|
Leukopenia
|
Disease
|
Inferred
|
Explain
|
0.02239
|
|
89
|
Mercilon
|
Compound
|
Inferred
|
Explain
|
0.02152
|
|
90
|
Thrombosis
|
Disease
|
Inferred
|
Explain
|
0.01971
|
|
91
|
Paraproteinemias
|
Disease
|
Inferred
|
Explain
|
0.01965
|
|
92
|
Hypoproteinemia
|
Disease
|
Inferred
|
Explain
|
0.01821
|
|
93
|
blood coagulation, intrinsic pathway
|
Function
|
Inferred
|
Explain
|
0.01583
|
|
94
|
HPS3 gene
|
Gene
|
Inferred
|
Explain
|
0.01540
|
|
95
|
HPS5 gene
|
Gene
|
Inferred
|
Explain
|
0.01540
|
|
96
|
Agammaglobulinemia
|
Disease
|
Inferred
|
Explain
|
0.01527
|
|
97
|
Albinism, Oculocutaneous
|
Other
|
Inferred
|
Explain
|
0.01502
|
|
98
|
Omeprazole
|
Compound
|
Inferred
|
Explain
|
0.01484
|
|
99
|
propylene dichloride
|
Compound
|
Inferred
|
Explain
|
0.01479
|
|
100
|
HPS6 gene
|
Gene
|
Inferred
|
Explain
|
0.01353
|
|