Search results for "hypofibrinogenemia"

The MalaCard for "hypofibrinogenemia" has been retired.
Searching MalaCards for entries containing "hypofibrinogenemia"

34 hits were found for 'hypofibrinogenemia'

# Family MCID Name MIFTS Score
1
P HYP295 Hypofibrinogenemia, Gamma Type 6 3.735
2
c HYP197 Hypofibrinogenemia, Familial 2 3.735
3
P CNG019 Congenital Afibrinogenemia 58 2.702
4
P DYS026 Dysfibrinogenemia 52 0.129
5
PLC007 Placental Abruption 50 0.129
6
c THR014 Thrombocytopenia 70 0.105
7
c HPT021 Hepatitis 64 0.105
8
HMP015 Hemophagocytic Reticulosis 9 0.105
9
P HYP075 Hypertension 85 0.074
10
P LKM002 Leukemia 77 0.074
11
VNW001 Von Willebrand's Disease 69 0.074
12
PRT014 Protein S Deficiency 67 0.074
13
c CHR090 Chronic Lymphocytic Leukemia 67 0.074
14
P HML002 Hemolytic Anemia 66 0.074
15
P THR015 Thrombophilia 66 0.074
16
PRP030 Purpura 64 0.074
17
FLT001 Felty's Syndrome 63 0.074
18
P HST010 Histiocytosis 62 0.074
19
URT039 Urticaria 61 0.074
20
c ATM010 Autoimmune Hemolytic Anemia 60 0.074
21
c AFB001 Afibrinogenemia 60 0.074
22
CHL067 Cholecystitis 60 0.074
23
SPT013 Septic Shock 60 0.074
24
c THR005 Thrombotic Thrombocytopenic Purpura 58 0.074
25
SPT005 Spotted Fever 52 0.074
26
MNN021 Meningococcemia 48 0.074
27
ILS001 Ileus 44 0.074
28
LKP004 Leukopenia 44 0.074
29
ACL001 Acalculous Cholecystitis 40 0.074
30
TRC023 Trichinosis 38 0.074
31
RCK002 Rocky Mountain Spotted Fever 36 0.074
32
PRL008 Paralytic Ileus 36 0.074
33
c HMP012 Hemophagocytic Lymphohistiocytosis, Familial, 2 28 0.074
34
MLL004 Mallory-Weiss Syndrome 21 0.074