Search results for "hypofibrinogenemia"

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

36 hits were found for 'hypofibrinogenemia'

# Family MCID Name MIFTS Score
1
P HYP588 Hypofibrinogenemia, Congenital 16 3.735
2
c HYP197 Hypofibrinogenemia, Familial 3 3.735
3
P CNG019 Congenital Afibrinogenemia 57 2.702
4
DYS026 Dysfibrinogenemia 63 0.146
5
c AFB001 Afibrinogenemia 62 0.127
6
PLC007 Placental Abruption 51 0.127
7
VNW001 Von Willebrand's Disease 72 0.104
8
c THR014 Thrombocytopenia 71 0.104
9
c HPT021 Hepatitis 64 0.104
10
HMP015 Hemophagocytic Reticulosis 9 0.104
11
P CHR090 Chronic Lymphocytic Leukemia 89 0.073
12
P HYP075 Hypertension 87 0.073
13
P LKM002 Leukemia 77 0.073
14
P THR015 Thrombophilia 67 0.073
15
PRP030 Purpura 66 0.073
16
c HML002 Hemolytic Anemia 66 0.073
17
PRT014 Protein S Deficiency 65 0.073
18
FLT001 Felty's Syndrome 64 0.073
19
URT039 Urticaria 64 0.073
20
P HST010 Histiocytosis 64 0.073
21
P ATM010 Autoimmune Hemolytic Anemia 62 0.073
22
CHL067 Cholecystitis 61 0.073
23
SPT013 Septic Shock 61 0.073
24
c THR005 Thrombotic Thrombocytopenic Purpura 59 0.073
25
SPT005 Spotted Fever 53 0.073
26
MNN021 Meningococcemia 48 0.073
27
ILS001 Ileus 45 0.073
28
LKP004 Leukopenia 45 0.073
29
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 42 0.073
30
ACL001 Acalculous Cholecystitis 41 0.073
31
TRC023 Trichinosis 40 0.073
32
RCK002 Rocky Mountain Spotted Fever 36 0.073
33
PRL008 Paralytic Ileus 36 0.073
34
c HMP012 Hemophagocytic Lymphohistiocytosis, Familial, 2 29 0.073
35
P HYP589 Hypodysfibrinogenemia 25 0.073
36
MLL004 Mallory-Weiss Syndrome 22 0.073