110 hits were found for 'FGA'

# Family MCID Name MIFTS Score
1
c FGR001 Fga-Related Congenital Afibrinogenemia 7 9.932
2
c FGR002 Fga-Related Familial Visceral Amyloidosis 4 9.932
3
c AFB001 Afibrinogenemia 48 4.332
4
P CNG019 Congenital Afibrinogenemia 59 3.690
5
P AMY004 Amyloidosis 65 3.290
6
P DYS026 Dysfibrinogenemia 41 3.266
7
CRB009 Cerebritis 56 2.695
8
THR079 Thromboembolism 50 2.695
9
P PRM021 Primary Pulmonary Hypertension 82 2.667
10
P ADL010 Adult Respiratory Distress Syndrome 71 2.667
11
ATH003 Atherosclerosis 71 2.667
12
DSS009 Disseminated Intravascular Coagulation 66 2.667
13
THR004 Thrombocytosis 63 2.667
14
PTN001 Patent Foramen Ovale 60 2.667
15
P CLL015 Collagen Disease 59 2.667
16
CRN017 Coronary Thrombosis 57 2.667
17
ANT009 Antithrombin Iii Deficiency 57 2.667
18
INT002 Intermittent Claudication 56 2.667
19
PLC005 Placental Insufficiency 44 2.667
20
CHR466 Chronic Thromboembolic Pulmonary Hypertension 43 2.667
21
VNS010 Venous Thromboembolism 42 2.667
22
HRD039 Hereditary Amyloidosis 35 2.667
23
AMY037 Amyloidosis, Hereditary Renal 26 2.667
24
P MYC007 Myocardial Infarction 88 2.310
25
P HYP075 Hypertension 86 2.310
26
P DLT002 Dilated Cardiomyopathy 82 2.310
27
c DBT009 Diabetes Mellitus 80 2.310
28
P LKM002 Leukemia 79 2.310
29
LVR012 Liver Cirrhosis 75 2.310
30
c LPS004 Lupus Erythematosus 73 2.310
31
VSC007 Vascular Disease 72 2.310
32
VSC011 Vasculitis 67 2.310
33
PRT014 Protein S Deficiency 66 2.310
34
P THR015 Thrombophilia 66 2.310
35
c NPH012 Nephrotic Syndrome 66 2.310
36
ISC004 Ischemia 64 2.310
37
c ACT073 Acute Leukemia 62 2.310
38
SCK005 Sickle Cell Disease 62 2.310
39
c ACT075 Acute Myocardial Infarction 61 2.310
40
P LYM026 Lymphoblastic Leukemia 56 2.310
41
c HYP095 Hypercholesterolemia 56 2.310
42
END072 Endotheliitis 47 2.310
43
P CRN157 Coronary Heart Disease 43 2.310
44
P FML003 Familial Visceral Amyloidosis 27 1.924
45
P PNC035 Pancreatic Cancer 95 1.886
46
P OBS005 Obesity 93 1.886
47
P PRS040 Prostate Cancer 91 1.886
48
HDG007 Hodgkin's Lymphoma 91 1.886
49
P SYS001 Systemic Lupus Erythematosus 87 1.886
50
CRH001 Crohn's Disease 83 1.886
51
AGR001 Age Related Macular Degeneration 83 1.886
52
P OVR042 Ovarian Cancer 79 1.886
53
P PNM007 Pneumonia 79 1.886
54
LSC001 Lesch-Nyhan Syndrome 79 1.886
55
PRT036 Peritonitis 78 1.886
56
c TYP008 Type 1 Diabetes Mellitus 77 1.886
57
P SCH015 Schizophrenia 77 1.886
58
PRC016 Pre-Eclampsia 75 1.886
59
c HPT021 Hepatitis 75 1.886
60
P LNG032 Lung Cancer 74 1.886
61
DBT011 Diabetic Retinopathy 73 1.886
62
CHL065 Cholangiocarcinoma 73 1.886
63
P CNG026 Congenital Heart Defect 73 1.886
64
SCH014 Schistosomiasis 72 1.886
65
CRN211 Coronary Artery Disease 72 1.886
66
NNH001 Non-Hodgkin Lymphoma 72 1.886
67
c ESS002 Essential Hypertension 71 1.886
68
P LVR013 Liver Disease 70 1.886
69
P TYP020 Type 1 Diabetes 69 1.886
70
ISC006 Ischemic Heart Disease 69 1.886
71
PLM033 Pulmonary Embolism 68 1.886
72
c THR014 Thrombocytopenia 67 1.886
73
c PNC044 Pancreatitis 67 1.886
74
HYP066 Hyperglycemia 65 1.886
75
c HPT016 Hepatitis B 65 1.886
76
ECL001 Eclampsia 63 1.886
77
PRS047 Prostatitis 62 1.886
78
CRB039 Cerebrovascular Disease 61 1.886
79
P CNJ013 Conjunctivitis 61 1.886
80
PSR002 Psoriasis 60 1.886
81
PRT011 Protein C Deficiency 60 1.886
82
P BRN019 Bernard-Soulier Syndrome 59 1.886
83
CLF001 Cleft Lip 59 1.886
84
SPS077 Sepsis 58 1.886
85
PRT039 Proteinuria 57 1.886
86
CRN030 Coronary Stenosis 53 1.886
87
P CRV039 Cervicitis 52 1.886
88
SPN186 Spinal Cord Injury 52 1.886
89
ANG054 Angina Pectoris 52 1.886
90
c ACT076 Acute Myocarditis 49 1.886
91
INT079 Intrahepatic Cholangiocarcinoma 43 1.886
92
VNS009 Venous Thrombosis 43 1.886
93
P ALZ001 Alzheimer's Disease 103 1.334
94
P MLT019 Multiple Myeloma 89 1.334
95
BRN106 Burns 64 1.334
96
CHL068 Cholestasis 63 1.334
97
P GRV001 Graves' Disease 63 1.334
98
c MYL007 Myeloma 59 1.334
99
P MYC008 Myocarditis 56 1.334
100
SPT013 Septic Shock 48 1.334
101
GLN002 Glanders 48 1.334
102
c GGN002 Gigantism 40 1.334
103
c FML259 Familial Renal Amyloidosis Due to Fibrinogen a Alpha-Chain Variant 14 1.334
104
DYS078 Dysfibrinogenemia, Alpha Type, Causing Recurrent Thrombosis 5 1.334
105
DYS077 Dysfibrinogenemia, Alpha Type, Causing Bleeding Diathesis 4 1.334
106
c FGB001 Fgb-Related Congenital Afibrinogenemia 5 0.280
107
TFT003 Tufting Enteropathy 21 0.134
108
MNN014 Mononeuritis 48 0.104
109
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.085
110
P ISC010 Isochromosome Yp 14 0.060