74 hits were found for 'FGB'

# Family MCID Name MIFTS Score
1
c FGB001 Fgb-Related Congenital Afibrinogenemia 5 10.691
2
c AFB001 Afibrinogenemia 48 5.462
3
P CNG019 Congenital Afibrinogenemia 59 3.992
4
P DYS026 Dysfibrinogenemia 41 3.633
5
PRP027 Peripheral Vascular Disease 75 2.966
6
PLM033 Pulmonary Embolism 68 2.966
7
P PRT013 Portal Hypertension 67 2.966
8
c HPT007 Hepatitis E 50 2.966
9
CHR466 Chronic Thromboembolic Pulmonary Hypertension 43 2.966
10
CRB009 Cerebritis 56 2.604
11
P MYC007 Myocardial Infarction 88 2.569
12
ATH003 Atherosclerosis 71 2.569
13
END072 Endotheliitis 47 2.569
14
VSC007 Vascular Disease 72 2.139
15
THR079 Thromboembolism 50 2.139
16
P ALZ001 Alzheimer's Disease 103 2.098
17
P AMY001 Amyotrophic Lateral Sclerosis 100 2.098
18
P OBS005 Obesity 93 2.098
19
P RHM011 Rheumatoid Arthritis 91 2.098
20
P FML021 Familial Hypercholesterolemia 87 2.098
21
P HYP075 Hypertension 86 2.098
22
CRH001 Crohn's Disease 83 2.098
23
AGR001 Age Related Macular Degeneration 83 2.098
24
c DBT009 Diabetes Mellitus 80 2.098
25
P ART022 Arthritis 75 2.098
26
c HPT021 Hepatitis 75 2.098
27
KWS002 Kawasaki Disease 74 2.098
28
P MGR002 Migraine 71 2.098
29
P TYP020 Type 1 Diabetes 69 2.098
30
ISC006 Ischemic Heart Disease 69 2.098
31
P THR015 Thrombophilia 66 2.098
32
P HPT001 Hepatitis C 66 2.098
33
P PRD008 Periodontitis 66 2.098
34
c HPT016 Hepatitis B 65 2.098
35
ISC004 Ischemia 64 2.098
36
CRB037 Cerebral Palsy 64 2.098
37
SCK005 Sickle Cell Disease 62 2.098
38
TNS005 Tonsillitis 62 2.098
39
RTN023 Retinitis 61 2.098
40
CRB039 Cerebrovascular Disease 61 2.098
41
c ACT075 Acute Myocardial Infarction 61 2.098
42
PSR002 Psoriasis 60 2.098
43
P RTN022 Retinal Vein Occlusion 59 2.098
44
c KDN018 Kidney Disease 58 2.098
45
P MYC008 Myocarditis 56 2.098
46
c HYP095 Hypercholesterolemia 56 2.098
47
P INF032 Infertility 56 2.098
48
HYP037 Hyperhomocysteinemia 55 2.098
49
c LTR001 Lateral Sclerosis 55 2.098
50
P INF037 Inflammatory Bowel Disease 50 2.098
51
LPS007 Lupus Nephritis 43 2.098
52
P CRN157 Coronary Heart Disease 43 2.098
53
VNS009 Venous Thrombosis 43 2.098
54
VNS010 Venous Thromboembolism 42 2.098
55
NPH051 Nephritis 39 2.098
56
c CRT018 Carotid Intimal Medial Thickness 37 2.098
57
CRN211 Coronary Artery Disease 72 1.580
58
P PRK002 Parkinson's Disease 92 1.483
59
P MLT019 Multiple Myeloma 89 1.483
60
c ESS002 Essential Hypertension 71 1.483
61
P PLY019 Polyneuropathy 64 1.483
62
c MYL007 Myeloma 59 1.483
63
SPS077 Sepsis 58 1.483
64
c GGN002 Gigantism 40 1.483
65
PRG060 Pregnancy Loss 38 1.483
66
c HPT073 Hepatitis C Virus 25 1.483
67
THR053 Thrombophilia, Dysfibrinogenemic 15 1.483
68
c DYS079 Dysfibrinogenemia, Beta Type 4 1.483
69
c FGR001 Fga-Related Congenital Afibrinogenemia 7 0.316
70
TFT003 Tufting Enteropathy 21 0.147
71
MNN014 Mononeuritis 48 0.114
72
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.093
73
FCT007 Factor Vii Deficiency 78 0.066
74
P ISC010 Isochromosome Yp 14 0.066