|
#
|
Concept name
|
Type
|
Relation
|
Support
|
Score
|
|
1
|
Protein S Deficiency
|
Disease
|
Known
|
Explain
|
31.36105
|
|
2
|
Hypergammaglobulinemia
|
Disease
|
Known
|
Explain
|
30.66810
|
|
3
|
Antithrombin III Deficiency
|
Disease
|
Known
|
Explain
|
29.40604
|
|
4
|
Protein C Deficiency
|
Disease
|
Known
|
Explain
|
27.19739
|
|
5
|
Dysgammaglobulinemia
|
Disease
|
Known
|
Explain
|
24.68523
|
|
6
|
Hypoproteinemia
|
Disease
|
Known
|
Explain
|
24.58762
|
|
7
|
Paraproteinemias
|
Disease
|
Known
|
Explain
|
23.22468
|
|
8
|
Agammaglobulinemia
|
Disease
|
Known
|
Explain
|
15.63046
|
|
9
|
SERPINA7 gene
|
Gene
|
Known
|
Explain
|
9.22153
|
|
10
|
Hematological Disease
|
Disease
|
Known
|
Explain
|
8.30450
|
|
11
|
Monoclonal Gammopathy of Undetermined Significance
|
Disease
|
Inferred
|
Explain
|
4.52401
|
|
12
|
Immunoproliferative Disorders
|
Disease
|
Inferred
|
Explain
|
4.24293
|
|
13
|
A2M gene
|
Gene
|
Known
|
Explain
|
3.82414
|
|
14
|
Thrombophilia
|
Disease
|
Inferred
|
Explain
|
3.12174
|
|
15
|
Deficiency of mevalonate kinase
|
Disease
|
Inferred
|
Explain
|
2.96673
|
|
16
|
Blood Coagulation Disorders, Inherited
|
Disease
|
Inferred
|
Explain
|
0.88680
|
|
17
|
Hypoalbuminemia
|
Disease
|
Inferred
|
Explain
|
0.73869
|
|
18
|
Signs and Symptoms
|
Disease
|
Inferred
|
Explain
|
0.66540
|
|
19
|
HYPOPROTEINEMIA, HYPERCATABOLIC
|
Disease
|
Inferred
|
Explain
|
0.65616
|
|
20
|
Hyperimmunoglobulin M syndrome
|
Disease
|
Inferred
|
Explain
|
0.65452
|
|
21
|
Lymphoproliferative Disorders
|
Disease
|
Inferred
|
Explain
|
0.62366
|
|
22
|
Blood Coagulation Disorders
|
Disease
|
Inferred
|
Explain
|
0.54417
|
|
23
|
Heavy Chain Disease
|
Disease
|
Inferred
|
Explain
|
0.42480
|
|
24
|
Cryoglobulinemia
|
Disease
|
Inferred
|
Explain
|
0.38798
|
|
25
|
Immunoglobulin A deficiency (disorder)
|
Disease
|
Inferred
|
Explain
|
0.38642
|
|
26
|
Hereditary Autoinflammatory Diseases
|
Disease
|
Inferred
|
Explain
|
0.35784
|
|
27
|
Mirex
|
Compound
|
Inferred
|
Explain
|
0.34901
|
|
28
|
POEMS Syndrome
|
Disease
|
Inferred
|
Explain
|
0.32970
|
|
29
|
Immune System Diseases
|
Disease
|
Inferred
|
Explain
|
0.31981
|
|
30
|
Immunologic Deficiency Syndromes
|
Disease
|
Inferred
|
Explain
|
0.29634
|
|
31
|
Waldenstrom Macroglobulinemia
|
Disease
|
Inferred
|
Explain
|
0.27657
|
|
32
|
Peroxisomal Disorders
|
Disease
|
Inferred
|
Explain
|
0.24833
|
|
33
|
Schnitzler Syndrome
|
Disease
|
Inferred
|
Explain
|
0.20922
|
|
34
|
IGKC gene
|
Gene
|
Inferred
|
Explain
|
0.19001
|
|
35
|
Hyper-IgM Immunodeficiency Syndrome, Type 1
|
Disease
|
Inferred
|
Explain
|
0.18977
|
|
36
|
SERPINC1 gene
|
Gene
|
Inferred
|
Explain
|
0.18767
|
|
37
|
ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA
|
Disease
|
Inferred
|
Explain
|
0.16990
|
|
38
|
PROC gene
|
Gene
|
Inferred
|
Explain
|
0.16612
|
|
39
|
MVK gene
|
Gene
|
Inferred
|
Explain
|
0.14756
|
|
40
|
Warfarin
|
Compound
|
Inferred
|
Explain
|
0.14602
|
|
41
|
Agammaglobulinemia, non-Bruton type
|
Disease
|
Inferred
|
Explain
|
0.13626
|
|
42
|
Furosemide
|
Compound
|
Inferred
|
Explain
|
0.12900
|
|
43
|
AGAMMAGLOBULINEMIA, X-LINKED, TYPE 2 (disorder)
|
Disease
|
Inferred
|
Explain
|
0.12238
|
|
44
|
Agammaglobulinemia, microcephaly, and severe dermatitis
|
Disease
|
Inferred
|
Explain
|
0.12121
|
|
45
|
Hemorrhagic Disorders
|
Disease
|
Inferred
|
Explain
|
0.10984
|
|
46
|
Immunoproliferative Small Intestinal Disease
|
Disease
|
Inferred
|
Explain
|
0.10206
|
|
47
|
Vascular Hemostatic Disorders
|
Disease
|
Inferred
|
Explain
|
0.09803
|
|
48
|
Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked
|
Disease
|
Inferred
|
Explain
|
0.08760
|
|
49
|
Activated Protein C Resistance
|
Disease
|
Inferred
|
Explain
|
0.08531
|
|
50
|
Multiple Myeloma
|
Disease
|
Inferred
|
Explain
|
0.07436
|
|
51
|
Coagulation Protein Disorders
|
Disease
|
Inferred
|
Explain
|
0.06955
|
|
52
|
Familial Mediterranean Fever
|
Disease
|
Inferred
|
Explain
|
0.06222
|
|
53
|
Disseminated Intravascular Coagulation
|
Disease
|
Inferred
|
Explain
|
0.05915
|
|
54
|
CD79B gene
|
Gene
|
Inferred
|
Explain
|
0.04560
|
|
55
|
Purpura, Thrombotic Thrombocytopenic
|
Disease
|
Inferred
|
Explain
|
0.04332
|
|
56
|
Blood Platelet Disorders
|
Disease
|
Inferred
|
Explain
|
0.04148
|
|
57
|
CD19 gene
|
Gene
|
Inferred
|
Explain
|
0.03833
|
|
58
|
IGHM gene
|
Gene
|
Inferred
|
Explain
|
0.03749
|
|
59
|
Blood Group Incompatibility
|
Disease
|
Inferred
|
Explain
|
0.03738
|
|
60
|
Pancytopenia
|
Disease
|
Inferred
|
Explain
|
0.03401
|
|
61
|
Sulfhemoglobinemia
|
Disease
|
Inferred
|
Explain
|
0.03050
|
|
62
|
Preleukemia
|
Disease
|
Inferred
|
Explain
|
0.02954
|
|
63
|
Leukocyte Disorders
|
Disease
|
Inferred
|
Explain
|
0.02895
|
|
64
|
Pregnancy Complications, Hematologic
|
Disease
|
Inferred
|
Explain
|
0.02894
|
|
65
|
Hematologic Neoplasms
|
Disease
|
Inferred
|
Explain
|
0.02890
|
|
66
|
Hemic and Lymphatic Diseases
|
Disease
|
Inferred
|
Explain
|
0.02889
|
|
67
|
Hemoglobinopathies
|
Disease
|
Inferred
|
Explain
|
0.02517
|
|
68
|
Mercilon
|
Compound
|
Inferred
|
Explain
|
0.02460
|
|
69
|
Gestodene
|
Compound
|
Inferred
|
Explain
|
0.02253
|
|
70
|
Bone Marrow Diseases
|
Disease
|
Inferred
|
Explain
|
0.02216
|
|
71
|
Polycythemia
|
Disease
|
Inferred
|
Explain
|
0.02132
|
|
72
|
Thrombosis
|
Disease
|
Inferred
|
Explain
|
0.02045
|
|
73
|
Genetic Diseases, Inborn
|
Disease
|
Inferred
|
Explain
|
0.01998
|
|
74
|
BTK gene
|
Gene
|
Inferred
|
Explain
|
0.01900
|
|
75
|
Polyneuropathy
|
Disease
|
Inferred
|
Explain
|
0.01822
|
|
76
|
Wiskott-Aldrich Syndrome
|
Disease
|
Inferred
|
Explain
|
0.01700
|
|
77
|
Hypoprothrombinemias
|
Disease
|
Inferred
|
Explain
|
0.01583
|
|
78
|
Factor V Deficiency
|
Disease
|
Inferred
|
Explain
|
0.01569
|
|
79
|
Factor VII Deficiency
|
Disease
|
Inferred
|
Explain
|
0.01562
|
|
80
|
Factor X Deficiency
|
Disease
|
Inferred
|
Explain
|
0.01544
|
|
81
|
Factor XI Deficiency
|
Disease
|
Inferred
|
Explain
|
0.01533
|
|
82
|
Factor XII Deficiency
|
Disease
|
Inferred
|
Explain
|
0.01506
|
|
83
|
Hemophilia B
|
Disease
|
Inferred
|
Explain
|
0.01478
|
|
84
|
Hydrops Fetalis
|
Disease
|
Inferred
|
Explain
|
0.01455
|
|
85
|
HABP2 gene
|
Gene
|
Inferred
|
Explain
|
0.01439
|
|
86
|
Factor XIII Deficiency
|
Disease
|
Inferred
|
Explain
|
0.01438
|
|
87
|
von Willebrand Disease
|
Disease
|
Inferred
|
Explain
|
0.01421
|
|
88
|
Afibrinogenemia
|
Disease
|
Inferred
|
Explain
|
0.01410
|
|
89
|
Thrombasthenia
|
Disease
|
Inferred
|
Explain
|
0.01368
|
|
90
|
Infantile Refsum Disease (disorder)
|
Disease
|
Inferred
|
Explain
|
0.01356
|
|
91
|
Methemoglobinemia
|
Disease
|
Inferred
|
Explain
|
0.01330
|
|
92
|
THBD gene
|
Gene
|
Inferred
|
Explain
|
0.01298
|
|
93
|
Thrombocytopenic purpura
|
Disease
|
Inferred
|
Explain
|
0.01290
|
|
94
|
3,5-dichlorobiphenyl
|
Compound
|
Inferred
|
Explain
|
0.01283
|
|
95
|
Gray Platelet Syndrome
|
Disease
|
Inferred
|
Explain
|
0.01259
|
|
96
|
Hemophilia A
|
Disease
|
Inferred
|
Explain
|
0.01249
|
|
97
|
Refsum Disease
|
Disease
|
Inferred
|
Explain
|
0.01230
|
|
98
|
F2 gene
|
Gene
|
Inferred
|
Explain
|
0.01229
|
|
99
|
XK gene
|
Gene
|
Inferred
|
Explain
|
0.01217
|
|
100
|
B2M gene
|
Gene
|
Inferred
|
Explain
|
0.01177
|