36 hits were found for 'FGG'

# Family MCID Name MIFTS Score
1
c FGG001 Fgg-Related Congenital Afibrinogenemia 4 11.419
2
P CNG019 Congenital Afibrinogenemia 59 4.863
3
P THR015 Thrombophilia 66 4.427
4
P DYS026 Dysfibrinogenemia 41 4.427
5
c AFB001 Afibrinogenemia 48 3.823
6
END072 Endotheliitis 47 3.130
7
THR079 Thromboembolism 50 2.606
8
P ALZ001 Alzheimer's Disease 103 2.556
9
HDG007 Hodgkin's Lymphoma 91 2.556
10
P MYC007 Myocardial Infarction 88 2.556
11
P HYP075 Hypertension 86 2.556
12
CRH001 Crohn's Disease 83 2.556
13
AGR001 Age Related Macular Degeneration 83 2.556
14
c HPT021 Hepatitis 75 2.556
15
NNH001 Non-Hodgkin Lymphoma 72 2.556
16
ATH003 Atherosclerosis 71 2.556
17
c HPT016 Hepatitis B 65 2.556
18
ISC004 Ischemia 64 2.556
19
c ACT075 Acute Myocardial Infarction 61 2.556
20
PSR002 Psoriasis 60 2.556
21
c KDN018 Kidney Disease 58 2.556
22
CRB009 Cerebritis 56 2.556
23
VNS010 Venous Thromboembolism 42 2.556
24
P MLT019 Multiple Myeloma 89 1.807
25
CRN211 Coronary Artery Disease 72 1.807
26
c MYL007 Myeloma 59 1.807
27
PRT018 Portal Vein Thrombosis 57 1.807
28
VNS009 Venous Thrombosis 43 1.807
29
THR053 Thrombophilia, Dysfibrinogenemic 15 1.807
30
c DYS080 Dysfibrinogenemia, Gamma Type 4 1.807
31
P HYP295 Hypofibrinogenemia, Gamma Type 4 1.807
32
c FGR001 Fga-Related Congenital Afibrinogenemia 7 0.380
33
TFT003 Tufting Enteropathy 21 0.177
34
MNN014 Mononeuritis 48 0.137
35
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.112
36
P ISC010 Isochromosome Yp 14 0.079