112 hits were found for 'FGA'

# ++ Fam MCID Name MIFTS Score
1
FGR001 Fga-Related Congenital Afibrinogenemia 6 9.922
2
FGR002 Fga-Related Familial Visceral Amyloidosis 2 9.922
3
c AFB001 Afibrinogenemia 52 4.429
4
P CNG019 Congenital Afibrinogenemia 52 3.673
5
P AMY004 Amyloidosis 65 3.275
6
P DYS026 Dysfibrinogenemia 46 3.252
7
THR079 Thromboembolism 63 2.709
8
VNS010 Venous Thromboembolism 54 2.683
9
P PRM021 Primary Pulmonary Hypertension 74 2.655
10
ATH003 Atherosclerosis 69 2.655
11
P ADL010 Adult Respiratory Distress Syndrome 66 2.655
12
THR004 Thrombocytosis 61 2.655
13
DSS009 Disseminated Intravascular Coagulation 59 2.655
14
PTN001 Patent Foramen Ovale 56 2.655
15
CRN017 Coronary Thrombosis 55 2.655
16
INT002 Intermittent Claudication 54 2.655
17
P CLL015 Collagen Disease 52 2.655
18
P CHR466 Chronic Thromboembolic Pulmonary Hypertension 51 2.655
19
CRB009 Cerebritis 46 2.655
20
ANT009 Antithrombin Iii Deficiency 43 2.655
21
PLC005 Placental Insufficiency 42 2.655
22
HRD039 Hereditary Amyloidosis 42 2.655
23
P MYC007 Myocardial Infarction 82 2.299
24
P HYP075 Hypertension 76 2.299
25
P DLT002 Dilated Cardiomyopathy 74 2.299
26
LKM002 Leukemia 70 2.299
27
VSC007 Vascular Disease 69 2.299
28
LVR012 Liver Cirrhosis 69 2.299
29
c DBT009 Diabetes Mellitus 68 2.299
30
PRT014 Protein S Deficiency 67 2.299
31
c LPS004 Lupus Erythematosus 65 2.299
32
P THR015 Thrombophilia 65 2.299
33
VSC011 Vasculitis 65 2.299
34
c HYP095 Hypercholesterolemia 65 2.299
35
ACT073 Acute Leukemia 62 2.299
36
c ACT075 Acute Myocardial Infarction 59 2.299
37
P CRN157 Coronary Heart Disease 59 2.299
38
SCK005 Sickle Cell Disease 58 2.299
39
c NPH012 Nephrotic Syndrome 57 2.299
40
ISC004 Ischemia 57 2.299
41
END072 Endotheliitis 51 2.299
42
LYM026 Lymphoblastic Leukemia 49 2.299
43
AMY037 Amyloidosis, Hereditary Renal 29 2.299
44
c FML003 Familial Visceral Amyloidosis 21 1.915
45
P SYS001 Systemic Lupus Erythematosus 83 1.877
46
P PNC035 Pancreatic Cancer 82 1.877
47
HDG007 Hodgkin's Lymphoma 80 1.877
48
P OBS005 Obesity 79 1.877
49
CRH001 Crohn's Disease 78 1.877
50
P PRS040 Prostate Cancer 76 1.877
51
P TYP020 Type 1 Diabetes 73 1.877
52
OVR042 Ovarian Cancer 73 1.877
53
c TYP008 Type 1 Diabetes Mellitus 71 1.877
54
AGR001 Age Related Macular Degeneration 71 1.877
55
P SCH015 Schizophrenia 69 1.877
56
CRN211 Coronary Artery Disease, 68 1.877
57
LSC001 Lesch-Nyhan Syndrome 68 1.877
58
P PNM007 Pneumonia 67 1.877
59
SPS077 Sepsis 67 1.877
60
PRT036 Peritonitis 67 1.877
61
c THR014 Thrombocytopenia 66 1.877
62
CLN016 Colon Cancer 66 1.877
63
DBT011 Diabetic Retinopathy 66 1.877
64
P CNG026 Congenital Heart Defect 65 1.877
65
c HPT021 Hepatitis 65 1.877
66
c ESS002 Essential Hypertension 64 1.877
67
PRC016 Pre-Eclampsia 64 1.877
68
SPN186 Spinal Cord Injury 63 1.877
69
P LVR013 Liver Disease 62 1.877
70
c HPT016 Hepatitis B 62 1.877
71
ISC006 Ischemic Heart Disease 62 1.877
72
ECL001 Eclampsia 62 1.877
73
LNG032 Lung Cancer 61 1.877
74
CHL065 Cholangiocarcinoma 61 1.877
75
PLM033 Pulmonary Embolism 60 1.877
76
SCH014 Schistosomiasis 59 1.877
77
HYP066 Hyperglycemia 59 1.877
78
PRT011 Protein C Deficiency 59 1.877
79
c PNC044 Pancreatitis 58 1.877
80
NNH001 Non-Hodgkin Lymphoma 58 1.877
81
P BRN019 Bernard-Soulier Syndrome 56 1.877
82
VNS009 Venous Thrombosis 56 1.877
83
P CNJ013 Conjunctivitis 55 1.877
84
CRB039 Cerebrovascular Disease 53 1.877
85
PSR002 Psoriasis 51 1.877
86
P PRT039 Proteinuria 51 1.877
87
PRS047 Prostatitis 50 1.877
88
ANG054 Angina Pectoris 48 1.877
89
CLF001 Cleft Lip 47 1.877
90
CRN030 Coronary Stenosis 47 1.877
91
c ACT076 Acute Myocarditis 47 1.877
92
P CRV039 Cervicitis 41 1.877
93
INT079 Intrahepatic Cholangiocarcinoma 34 1.877
94
P ALZ001 Alzheimer's Disease 93 1.327
95
P TYP009 Type 2 Diabetes Mellitus 80 1.327
96
P MLT019 Multiple Myeloma 76 1.327
97
P GRV001 Graves' Disease 63 1.327
98
SPT013 Septic Shock 62 1.327
99
BRN106 Burns 61 1.327
100
CHL068 Cholestasis 55 1.327
101
c MYL007 Myeloma 53 1.327
102
c GGN002 Gigantism 51 1.327
103
P MYC008 Myocarditis 51 1.327
104
GLN002 Glanders 44 1.327
105
FML258 Familial Renal Amyloidosis Due to Fibrinogen a Alpha-Chain Variant 7 1.327
106
DYS077 Dysfibrinogenemia, Alpha Type, Causing Bleeding Diathesis 3 1.327
107
DYS078 Dysfibrinogenemia, Alpha Type, Causing Recurrent Thrombosis 3 1.327
108
FGB001 Fgb-Related Congenital Afibrinogenemia 4 0.286
109
TFT003 Tufting Enteropathy 26 0.133
110
MNN014 Mononeuritis 40 0.103
111
P DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 23 0.084
112
P ISC010 Isochromosome Yp 14 0.060