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

113 hits were found for 'alloimmunization'

# ++ Fam MCID Name MIFTS Score
1
FTL012 Fetal and Neonatal Alloimmune Thrombocytopenia 26 4.832
2
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 14 4.581
3
NTR014 Neutropenia, Alloimmune Neonatal 9 4.119
4
THR095 Thrombocytopenia, Neonatal Alloimmune 13 3.709
5
THR094 Thrombocytopenia, Neonatal Alloimmune, Bak Antigen Related 3 3.239
6
c MMB010 Membranous Congenital Glomerulonephritis Due to Anti-Maternal Neutral Endopeptidase Alloimmunization 1 3.239
7
ATM004 Autoimmune Thrombocytopenic Purpura 62 2.368
8
c THR014 Thrombocytopenia 66 0.349
9
THR013 Thoracic Outlet Syndrome 53 0.206
10
SDR002 Siderosis 50 0.192
11
THR035 Thrombasthenia 49 0.192
12
c NTR004 Neutropenia 59 0.160
13
SCK005 Sickle Cell Disease 58 0.160
14
DND005 Dandy-Walker Complex 22 0.160
15
PRP030 Purpura 60 0.151
16
VND002 Van Der Woude Syndrome 34 0.151
17
FCT013 Factor V Leiden Thrombophilia 31 0.151
18
NNT016 Neonatal Hemochromatosis 41 0.141
19
RPP001 Rapp-Hodgkin Syndrome 37 0.141
20
BLD122 Bleeding Disorder, Platelet-Type, 16, Autosomal Dominant 23 0.130
21
RPD005 Rapidly Involuting Congenital Hemangioma 19 0.130
22
ANK002 Ankylosing Spondylitis 75 0.119
23
HYD012 Hydrops Fetalis 61 0.119
24
P CNG052 Congenital Amegakaryocytic Thrombocytopenia 45 0.119
25
HNM001 Hinman's Syndrome 28 0.119
26
TFT003 Tufting Enteropathy 26 0.119
27
ATX002 Ataxia Telangiectasia 81 0.106
28
P HMC003 Hemochromatosis 73 0.106
29
SCK003 Sickle Cell Anemia 67 0.106
30
P GRF002 Graft Versus Host Disease 64 0.106
31
c ESS003 Essential Thrombocythemia 60 0.106
32
HML002 Hemolytic Anemia 60 0.106
33
GRY002 Gray Platelet Syndrome 51 0.106
34
LKM002 Leukemia 70 0.092
35
THL005 Thalassemia 69 0.092
36
GLN003 Glanzmann's Thrombasthenia 68 0.092
37
P HMP004 Hemophilia B 66 0.092
38
P LVR013 Liver Disease 62 0.092
39
THR004 Thrombocytosis 61 0.092
40
c NPH012 Nephrotic Syndrome 57 0.092
41
HPR003 Heparin-Induced Thrombocytopenia 55 0.092
42
P PNC001 Pancytopenia 55 0.092
43
P CHR092 Chronic Myeloproliferative Disease 48 0.092
44
c OPT004 Optic Atrophy 41 0.092
45
c PRM041 Primary Cortisol Resistance 19 0.092
46
AND002 Androgen Insensitivity Syndrome 75 0.075
47
ACN002 Acanthosis Nigricans 70 0.075
48
ALP006 Alpha Thalassemia 68 0.075
49
WST001 West Syndrome 64 0.075
50
c AXN002 Axenfeld-Rieger Syndrome 57 0.075
51
MYC002 Mycobacterium Avium Complex Disease 56 0.075
52
ATM010 Autoimmune Hemolytic Anemia 55 0.075
53
c MYL014 Myeloproliferative Disorder 54 0.075
54
SPL018 Splenomegaly 50 0.075
55
c CHR417 Chronic Graft Versus Host Disease 49 0.075
56
P THR090 Thrombocythemia 1 48 0.075
57
c PRN026 Porencephaly 40 0.075
58
OP3001 Opa3-Related 3-Methylglutaconic Aciduria 36 0.075
59
PMP002 Pemphigoid Gestationis 35 0.075
60
P DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 23 0.075
61
FTL004 Fetal Erythroblastosis 19 0.075
62
RHM007 Rheumatic Congestive Heart Failure 19 0.075
63
c KRN003 Kernicterus Due to Isoimmunization 18 0.075
64
PLY001 Polycythemia Vera 77 0.053
65
APL001 Aplastic Anemia 77 0.053
66
LVR012 Liver Cirrhosis 69 0.053
67
P MYL005 Myelofibrosis 67 0.053
68
P ANG001 Angelman Syndrome 67 0.053
69
P HPT001 Hepatitis C 66 0.053
70
c HPT021 Hepatitis 65 0.053
71
BLL006 Bullous Pemphigoid 65 0.053
72
ART019 Aortic Valve Stenosis 64 0.053
73
c HMP007 Hemophilia 64 0.053
74
CHR012 Chronic Granulomatous Disease 63 0.053
75
BRN002 Bronchiolitis 60 0.053
76
P GLM007 Glomerulonephritis 60 0.053
77
P BRN012 Bronchiolitis Obliterans 58 0.053
78
c HPT003 Hepatitis a 57 0.053
79
NSY001 N Syndrome 57 0.053
80
P BRN019 Bernard-Soulier Syndrome 56 0.053
81
HPT022 Hepatoblastoma 56 0.053
82
c EMR001 Emery-Dreifuss Muscular Dystrophy 56 0.053
83
c ACT135 Acute Graft Versus Host Disease 55 0.053
84
VNW001 Von Willebrand's Disease 55 0.053
85
CHL068 Cholestasis 55 0.053
86
P CNJ013 Conjunctivitis 55 0.053
87
THR009 Thrombocytopenia-Absent Radius Syndrome 55 0.053
88
THY033 Thyrotoxicosis 55 0.053
89
PLY018 Polycythemia 55 0.053
90
NPH051 Nephritis 55 0.053
91
ALL009 Allergic Conjunctivitis 55 0.053
92
HST011 Histoplasmosis 54 0.053
93
PRT018 Portal Vein Thrombosis 54 0.053
94
CHR285 Chronic Myelomonocytic Leukemia 53 0.053
95
CHR005 Chorioamnionitis 52 0.053
96
c CNT035 Central Nervous System Disease 52 0.053
97
ART001 Arterial Tortuosity Syndrome 52 0.053
98
TCL004 T-Cell Leukemia 50 0.053
99
c PRG060 Pregnancy Loss 48 0.053
100
HMT018 Hematopoietic Stem Cell Transplantation 41 0.053
101
GRN017 Granulocytopenia 41 0.053
102
AND003 Andersen-Tawil Syndrome 39 0.053
103
HRP002 Herpes Gestationis 37 0.053
104
HYD028 Hydrops, Ectopic Calcification, Moth-Eaten Skeletal Dysplasia 37 0.053
105
EMN001 Emanuel Syndrome 34 0.053
106
c ATX010 Ataxia Neuropathy Spectrum 33 0.053
107
ADS002 Adie Syndrome 32 0.053
108
LKM004 Leukemia, B-Cell, Chronic 29 0.053
109
c HMP017 Hemophilia a, Congenital 26 0.053
110
AND005 Androgen Insensitivity Syndrome, Mild 19 0.053
111
LKM005 Leukemia, T-Cell, Chronic 18 0.053
112
c BNG076 Benign Exophthalmos Syndrome 17 0.053
113
P ISC010 Isochromosome Yp 14 0.053