36 hits were found for 'FGG'

# ++ Fam MCID Name MIFTS Score
1
FGG001 Fgg-Related Congenital Afibrinogenemia 3 11.426
2
P CNG019 Congenital Afibrinogenemia 52 4.867
3
P THR015 Thrombophilia 65 4.430
4
P DYS026 Dysfibrinogenemia 46 4.430
5
c AFB001 Afibrinogenemia 52 3.872
6
END072 Endotheliitis 51 3.133
7
THR079 Thromboembolism 63 2.608
8
P ALZ001 Alzheimer's Disease 93 2.558
9
P MYC007 Myocardial Infarction 82 2.558
10
HDG007 Hodgkin's Lymphoma 80 2.558
11
CRH001 Crohn's Disease 78 2.558
12
P HYP075 Hypertension 76 2.558
13
AGR001 Age Related Macular Degeneration 71 2.558
14
ATH003 Atherosclerosis 69 2.558
15
c HPT021 Hepatitis 65 2.558
16
c HPT016 Hepatitis B 62 2.558
17
c ACT075 Acute Myocardial Infarction 59 2.558
18
NNH001 Non-Hodgkin Lymphoma 58 2.558
19
ISC004 Ischemia 57 2.558
20
VNS010 Venous Thromboembolism 54 2.558
21
c KDN018 Kidney Disease 52 2.558
22
PSR002 Psoriasis 51 2.558
23
CRB009 Cerebritis 46 2.558
24
VNS009 Venous Thrombosis 56 1.874
25
P MLT019 Multiple Myeloma 76 1.809
26
CRN211 Coronary Artery Disease, 68 1.809
27
PRT018 Portal Vein Thrombosis 54 1.809
28
c MYL007 Myeloma 53 1.809
29
THR053 Thrombophilia, Dysfibrinogenemic 11 1.809
30
c DYS080 Dysfibrinogenemia, Gamma Type 3 1.809
31
P HYP295 Hypofibrinogenemia, Gamma Type 3 1.809
32
FGR001 Fga-Related Congenital Afibrinogenemia 6 0.389
33
TFT003 Tufting Enteropathy 26 0.177
34
MNN014 Mononeuritis 40 0.137
35
P DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 23 0.112
36
P ISC010 Isochromosome Yp 14 0.079