Search results for "[genes] ADAMTS13"

33 hits were found for '[genes] ADAMTS13'

# Family MCID Name MIFTS Score
1
PRP030 Purpura 59 19.416
2
c THR054 Thrombotic Thrombocytopenic Purpura, Familial 44 19.416
3
P THR005 Thrombotic Thrombocytopenic Purpura 55 17.976
4
P THR014 Thrombocytopenia 64 16.410
5
P HML002 Hemolytic Anemia 60 16.410
6
c SYS001 Systemic Lupus Erythematosus 87 14.677
7
MLR004 Malaria 79 14.677
8
VNW001 Von Willebrand's Disease 61 14.677
9
CNN005 Connective Tissue Disease 61 14.677
10
ALC006 Alcoholic Hepatitis 59 14.677
11
P ANT006 Antiphospholipid Syndrome 58 14.677
12
DSS009 Disseminated Intravascular Coagulation 51 14.677
13
P HML001 Hemolytic-Uremic Syndrome 50 14.677
14
HLL004 Hellp Syndrome 49 14.677
15
c MLG069 Malignant Hypertension 47 14.677
16
P MYC007 Myocardial Infarction 79 12.711
17
c ACT071 Acute Kidney Failure 50 12.711
18
BLR008 Bilirubin Metabolic Disorder 47 12.711
19
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 43 12.711
20
EVN001 Evans' Syndrome 43 12.711
21
P HMR003 Hemorrhagic Disease 57 10.378
22
BLD053 Blood Platelet Disease 46 10.378
23
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 46 10.378
24
P BLD051 Blood Coagulation Disease 45 10.378
25
c WLL027 Weill-Marchesani Syndrome 1, Recessive 44 10.378
26
c PRM225 Primary Thrombocytopenia 42 10.378
27
CTS005 Catastrophic Antiphospholipid Syndrome 41 10.378
28
CRT008 Carotid Artery Dissection 41 10.378
29
DYS003 Dysgraphia 38 10.378
30
ATM012 Autoimmune Disease of Blood 37 10.378
31
TYP015 Type 2b Von Willebrand Disease 30 10.378
32
IMM136 Immune System Disease 50 7.339
33
FML151 Familial Thrombotic Thrombocytopenia Purpura 8 7.339