Search results for "hypofibrinogenemia"

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

40 hits were found for 'hypofibrinogenemia'

# Family MCID Name MIFTS Score
1
c AFB002 Afibrinogenemia, Congenital 54 5.960
2
HYP197 Hypofibrinogenemia, Familial 2 2.731
3
P AFB001 Afibrinogenemia 46 2.686
4
P HPT021 Hepatitis 70 0.123
5
PLC007 Placental Abruption 47 0.123
6
P DYS026 Dysfibrinogenemia 41 0.123
7
P THR014 Thrombocytopenia 64 0.100
8
VNW001 Von Willebrand's Disease 61 0.100
9
LTT002 Letterer-Siwe Disease 54 0.100
10
PRT014 Protein S Deficiency 52 0.100
11
c HMP012 Hemophagocytic Lymphohistiocytosis, Familial, 2 31 0.100
12
c HMP014 Hemophagocytic Lymphohistiocytosis, Familial, 4 29 0.100
13
HMP015 Hemophagocytic Reticulosis 8 0.100
14
c CHR090 Chronic Lymphocytic Leukemia 74 0.071
15
P LVR013 Liver Disease 72 0.071
16
P LKM002 Leukemia 70 0.071
17
P NRB001 Neuroblastoma 69 0.071
18
P HML002 Hemolytic Anemia 60 0.071
19
c ATM010 Autoimmune Hemolytic Anemia 60 0.071
20
P THR015 Thrombophilia 59 0.071
21
PRP030 Purpura 59 0.071
22
URT039 Urticaria 59 0.071
23
SPT005 Spotted Fever 56 0.071
24
CHL067 Cholecystitis 56 0.071
25
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.071
26
P HST010 Histiocytosis 55 0.071
27
P TRT010 Teratoma 52 0.071
28
TRC023 Trichinosis 43 0.071
29
RCK002 Rocky Mountain Spotted Fever 43 0.071
30
FCT005 Factor Xiii Deficiency 42 0.071
31
PRL008 Paralytic Ileus 39 0.071
32
MNN021 Meningococcemia 38 0.071
33
ACL001 Acalculous Cholecystitis 36 0.071
34
c DYS165 Dysfibrinogenemia, Congenital 34 0.071
35
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 34 0.071
36
c LYM114 Lymphoproliferative Syndrome, X-Linked, 2 30 0.071
37
ADR003 Adrenal Neuroblastoma 28 0.071
38
c HMP013 Hemophagocytic Lymphohistiocytosis, Familial, 3 28 0.071
39
MLL004 Mallory-Weiss Syndrome 25 0.071
40
CRP004 Corpus Luteum Cyst 23 0.071