Search results for "alloimmunization"

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

82 hits were found for 'alloimmunization'

# Family MCID Name MIFTS Score
1
FTL012 Fetal and Neonatal Alloimmune Thrombocytopenia 30 5.033
2
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 17 4.858
3
CNG407 Congenital Membranous Nephropathy Due to Maternal Anti-Neutral Endopeptidase Alloimmunization 8 4.858
4
HML043 Hemolytic Disease of the Newborn with Kell Alloimmunization 4 4.215
5
THR100 Thrombocytopenic Purpura, Autoimmune 35 2.463
6
P THR014 Thrombocytopenia 56 0.384
7
P NTR004 Neutropenia 56 0.217
8
SCK005 Sickle Cell Disease 54 0.174
9
P THL005 Thalassemia 64 0.153
10
PRP030 Purpura 54 0.142
11
NNT016 Neonatal Hemochromatosis 41 0.142
12
P HMC003 Hemochromatosis 75 0.130
13
P LVR013 Liver Disease 62 0.130
14
P HML002 Hemolytic Anemia 56 0.130
15
HYD012 Hydrops Fetalis 53 0.130
16
SCK003 Sickle Cell Anemia 70 0.116
17
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 38 0.116
18
c ATM010 Autoimmune Hemolytic Anemia 57 0.100
19
THR013 Thoracic Outlet Syndrome 45 0.100
20
END072 Endotheliitis 44 0.100
21
THR035 Thrombasthenia 37 0.100
22
P LKM002 Leukemia 66 0.082
23
GLN010 Glanzmann Thrombasthenia 63 0.082
24
P SDR002 Siderosis 49 0.082
25
P PRN026 Porencephaly 48 0.082
26
P PNC001 Pancytopenia 41 0.082
27
P TRC086 Trichohepatoenteric Syndrome 1 39 0.082
28
c CHR417 Chronic Graft Versus Host Disease 37 0.082
29
HMT018 Hematopoietic Stem Cell Transplantation 36 0.082
30
FTL004 Fetal Erythroblastosis 17 0.082
31
P APL001 Aplastic Anemia 76 0.058
32
P ATX030 Ataxia-Telangiectasia 76 0.058
33
PLY001 Polycythemia Vera 75 0.058
34
P PRM002 Primary Hyperoxaluria 68 0.058
35
AND015 Androgen Insensitivity 69 0.058
36
P MYL005 Myelofibrosis 68 0.058
37
P ESS003 Essential Thrombocythemia 66 0.058
38
MYL009 Myelodysplastic Syndrome 67 0.058
39
LVR012 Liver Cirrhosis 66 0.058
40
c HMP029 Hemophilia a 66 0.058
41
CHR012 Chronic Granulomatous Disease 64 0.058
42
HST011 Histoplasmosis 64 0.058
43
P NPH012 Nephrotic Syndrome 60 0.058
44
P HMP007 Hemophilia 59 0.058
45
P PLY018 Polycythemia 58 0.058
46
ART021 Arteriosclerosis 58 0.058
47
P HPT021 Hepatitis 55 0.058
48
GRY002 Gray Platelet Syndrome 54 0.058
49
P AND016 Andersen Syndrome 54 0.058
50
HPT022 Hepatoblastoma 53 0.058
51
P CNJ013 Conjunctivitis 53 0.058
52
BRN002 Bronchiolitis 52 0.058
53
MYC002 Mycobacterium Avium Complex Disease 51 0.058
54
BRN012 Bronchiolitis Obliterans 50 0.058
55
CHL068 Cholestasis 50 0.058
56
THR004 Thrombocytosis 50 0.058
57
P AXN010 Axenfeld-Rieger Syndrome, Type 3 50 0.058
58
THY033 Thyrotoxicosis 49 0.058
59
VND002 Van Der Woude Syndrome 48 0.058
60
ART001 Arterial Tortuosity Syndrome 48 0.058
61
c CHR285 Chronic Myelomonocytic Leukemia 48 0.058
62
NPH051 Nephritis 46 0.058
63
HMR001 Hemorrhagic Thrombocythemia 46 0.058
64
RPP001 Rapp-Hodgkin Syndrome 45 0.058
65
c CHR092 Chronic Myeloproliferative Disease 43 0.058
66
GRN017 Granulocytopenia 42 0.058
67
CHR005 Chorioamnionitis 42 0.058
68
P ART084 Arteriovenous Fistula 40 0.058
69
SPL018 Splenomegaly 40 0.058
70
ALL009 Allergic Conjunctivitis 40 0.058
71
MMB002 Membranous Glomerulonephritis 40 0.058
72
PMP002 Pemphigoid Gestationis 36 0.058
73
FCT013 Factor V Leiden Thrombophilia 31 0.058
74
RHM028 Rheumatic Heart Disease 32 0.058
75
ADS002 Adie Syndrome 30 0.058
76
TFT003 Tufting Enteropathy 26 0.058
77
HNM002 Hinman Syndrome 26 0.058
78
MMB005 Membranous Glomerulonephritis, Antenatal 21 0.058
79
c BNG076 Benign Exophthalmos Syndrome 19 0.058
80
HRD137 Hereditary Isolated Aplastic Anemia 17 0.058
81
AND005 Androgen Insensitivity Syndrome, Mild 17 0.058
82
TRN013 Transient Neonatal Thrombocytopenia 6 0.058