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

86 hits were found for 'alloimmunization'

# Family MCID Name MIFTS Score
1
FTL012 Fetal and Neonatal Alloimmune Thrombocytopenia 32 4.783
2
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 20 4.624
3
NTR014 Neutropenia, Alloimmune Neonatal 7 3.981
4
THR095 Thrombocytopenia, Neonatal Alloimmune 8 3.453
5
THR094 Thrombocytopenia, Neonatal Alloimmune, Bak Antigen Related 5 3.250
6
c MMB010 Membranous Congenital Glomerulonephritis Due to Anti-Maternal Neutral Endopeptidase Alloimmunization 3 3.250
7
ATM004 Autoimmune Thrombocytopenic Purpura 68 2.383
8
c THR014 Thrombocytopenia 67 0.376
9
THR013 Thoracic Outlet Syndrome 54 0.201
10
SCK005 Sickle Cell Disease 62 0.174
11
PRP030 Purpura 67 0.164
12
c NTR004 Neutropenia 65 0.164
13
FCT013 Factor V Leiden Thrombophilia 35 0.164
14
NNT016 Neonatal Hemochromatosis 44 0.153
15
RPP001 Rapp-Hodgkin Syndrome 34 0.153
16
ANK002 Ankylosing Spondylitis 75 0.130
17
P CNG052 Congenital Amegakaryocytic Thrombocytopenia 45 0.130
18
P ATX002 Ataxia Telangiectasia 93 0.116
19
P HMC003 Hemochromatosis 80 0.116
20
SCK003 Sickle Cell Anemia 73 0.116
21
P HML002 Hemolytic Anemia 68 0.116
22
P GRF002 Graft Versus Host Disease 65 0.116
23
GRY002 Gray Platelet Syndrome 51 0.116
24
c ESS003 Essential Thrombocythemia 50 0.116
25
HNM002 Hinman Syndrome 24 0.116
26
P HMP004 Hemophilia B 80 0.100
27
P LKM002 Leukemia 79 0.100
28
P LVR013 Liver Disease 70 0.100
29
c THL005 Thalassemia 68 0.100
30
c NPH012 Nephrotic Syndrome 66 0.100
31
THR004 Thrombocytosis 63 0.100
32
P PNC001 Pancytopenia 55 0.100
33
P CHR092 Chronic Myeloproliferative Disease 55 0.100
34
EVN001 Evans' Syndrome 54 0.100
35
HPR003 Heparin-Induced Thrombocytopenia 45 0.100
36
SYN053 Syndromic Diarrhea 42 0.100
37
AND002 Androgen Insensitivity Syndrome 88 0.082
38
P ALP006 Alpha Thalassemia 75 0.082
39
WST001 West Syndrome 64 0.082
40
c AXN002 Axenfeld-Rieger Syndrome 60 0.082
41
c ATM010 Autoimmune Hemolytic Anemia 57 0.082
42
MYC002 Mycobacterium Avium Complex Disease 57 0.082
43
P THR090 Thrombocythemia 1 54 0.082
44
SDR002 Siderosis 53 0.082
45
P HYP141 Hyperphenylalaninemia 49 0.082
46
c MYL014 Myeloproliferative Disorder 39 0.082
47
SPL018 Splenomegaly 37 0.082
48
P KRN003 Kernicterus Due to Isoimmunization 21 0.082
49
RHM007 Rheumatic Congestive Heart Failure 21 0.082
50
FTL004 Fetal Erythroblastosis 20 0.082
51
P APL001 Aplastic Anemia 83 0.058
52
PLY001 Polycythemia Vera 83 0.058
53
GLN003 Glanzmann's Thrombasthenia 80 0.058
54
LVR012 Liver Cirrhosis 75 0.058
55
P MYL005 Myelofibrosis 75 0.058
56
c HPT021 Hepatitis 75 0.058
57
VNW001 Von Willebrand's Disease 74 0.058
58
CHR012 Chronic Granulomatous Disease 72 0.058
59
P ANG001 Angelman Syndrome 70 0.058
60
ART019 Aortic Valve Stenosis 68 0.058
61
c HMP007 Hemophilia 68 0.058
62
P GLM007 Glomerulonephritis 66 0.058
63
HST011 Histoplasmosis 65 0.058
64
HPT022 Hepatoblastoma 65 0.058
65
CHL068 Cholestasis 63 0.058
66
ART001 Arterial Tortuosity Syndrome 62 0.058
67
c PLY018 Polycythemia 61 0.058
68
P CNJ013 Conjunctivitis 61 0.058
69
BRN002 Bronchiolitis 61 0.058
70
THR009 Thrombocytopenia-Absent Radius Syndrome 60 0.058
71
c HPT003 Hepatitis a 60 0.058
72
BRN012 Bronchiolitis Obliterans 59 0.058
73
P BRN019 Bernard-Soulier Syndrome 59 0.058
74
ALL009 Allergic Conjunctivitis 59 0.058
75
THY033 Thyrotoxicosis 58 0.058
76
PRT018 Portal Vein Thrombosis 57 0.058
77
CHR005 Chorioamnionitis 56 0.058
78
c ART084 Arteriovenous Fistula 47 0.058
79
c OPT004 Optic Atrophy 46 0.058
80
HYD028 Hydrops, Ectopic Calcification, Moth-Eaten Skeletal Dysplasia 43 0.058
81
AND003 Andersen-Tawil Syndrome 43 0.058
82
ADS002 Adie Syndrome 33 0.058
83
c HMP017 Hemophilia a, Congenital 21 0.058
84
c BNG076 Benign Exophthalmos Syndrome 21 0.058
85
AND005 Androgen Insensitivity Syndrome, Mild 18 0.058
86
TRN013 Transient Neonatal Thrombocytopenia 9 0.058