Search results for "FGA"

35 hits were found for 'FGA'

# Family MCID Name MIFTS Score
1
c FGR001 Fga-Related Congenital Afibrinogenemia 8 9.129
2
c FGR002 Fga-Related Familial Visceral Amyloidosis 8 9.129
3
DYS026 Dysfibrinogenemia 63 6.376
4
c AFB001 Afibrinogenemia 62 5.761
5
P CNG019 Congenital Afibrinogenemia 57 4.760
6
P AMY004 Amyloidosis 68 4.540
7
THR079 Thromboembolism 66 3.754
8
P FML003 Familial Visceral Amyloidosis 42 3.719
9
P PRM021 Primary Pulmonary Hypertension 77 3.681
10
c PLM037 Pulmonary Hypertension 73 3.681
11
PRT014 Protein S Deficiency 65 3.681
12
DSS009 Disseminated Intravascular Coagulation 62 3.681
13
THR004 Thrombocytosis 61 3.681
14
P AMY038 Amyloidosis, Renal 35 3.188
15
AMY034 Amyloidosis, 3 or More Types 29 3.188
16
VNS010 Venous Thromboembolism 55 2.655
17
P MYC007 Myocardial Infarction 93 2.603
18
LSC001 Lesch-Nyhan Syndrome 78 2.603
19
P BRN019 Bernard-Soulier Syndrome 65 2.603
20
PTN001 Patent Foramen Ovale 62 2.603
21
CRN017 Coronary Thrombosis 60 2.603
22
ANT009 Antithrombin Iii Deficiency 59 2.603
23
INT002 Intermittent Claudication 55 2.603
24
P CLL015 Collagen Disease 50 2.603
25
c HRD039 Hereditary Amyloidosis 48 2.603
26
ANG054 Angina Pectoris 47 2.603
27
CRN030 Coronary Stenosis 43 2.603
28
CHR466 Chronic Thromboembolic Pulmonary Hypertension 43 2.603
29
P HYP589 Hypodysfibrinogenemia 25 2.603
30
c FML259 Familial Renal Amyloidosis Due to Fibrinogen a Alpha-Chain Variant 11 1.841
31
c HYP587 Hypodysfibrinogenemia, Congenital 3 1.841
32
MNN014 Mononeuritis 51 0.081
33
CRB009 Cerebritis 39 0.081
34
TFT003 Tufting Enteropathy 28 0.081
35
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.081