Search results for "alloimmunization"

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

96 hits were found for 'alloimmunization'

# Family MCID Name MIFTS Score
1
FTL012 Fetal and Neonatal Alloimmune Thrombocytopenia 34 4.780
2
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 21 4.599
3
CNG407 Congenital Membranous Nephropathy Due to Maternal Anti-Neutral Endopeptidase Alloimmunization 7 4.599
4
NTR014 Neutropenia, Alloimmune Neonatal 8 3.983
5
HML043 Hemolytic Disease of the Newborn with Kell Alloimmunization 4 3.983
6
THR095 Thrombocytopenia, Neonatal Alloimmune 8 3.369
7
THR094 Thrombocytopenia, Neonatal Alloimmune, Bak Antigen Related 5 3.252
8
c THR014 Thrombocytopenia 71 0.377
9
c NTR004 Neutropenia 64 0.218
10
c NNT047 Neonatal Neutropenia 27 0.195
11
SCK005 Sickle Cell Disease 62 0.169
12
NNT016 Neonatal Hemochromatosis 48 0.149
13
PRP030 Purpura 66 0.138
14
c HML002 Hemolytic Anemia 66 0.126
15
HYD012 Hydrops Fetalis 62 0.126
16
P HMC003 Hemochromatosis 83 0.112
17
SCK003 Sickle Cell Anemia 82 0.112
18
c THL005 Thalassemia 72 0.112
19
P LVR013 Liver Disease 69 0.112
20
P GRF002 Graft Versus Host Disease 65 0.112
21
THR013 Thoracic Outlet Syndrome 52 0.112
22
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 42 0.112
23
P ATM010 Autoimmune Hemolytic Anemia 62 0.097
24
END072 Endotheliitis 51 0.097
25
THR035 Thrombasthenia 45 0.097
26
SYN053 Syndromic Diarrhea 34 0.097
27
AND002 Androgen Insensitivity Syndrome 80 0.079
28
P LKM002 Leukemia 77 0.079
29
P ALP006 Alpha Thalassemia 75 0.079
30
c AXN002 Axenfeld-Rieger Syndrome 67 0.079
31
P SDR002 Siderosis 58 0.079
32
P PNC001 Pancytopenia 48 0.079
33
c PRN026 Porencephaly 48 0.079
34
c CHR417 Chronic Graft Versus Host Disease 43 0.079
35
HMT018 Hematopoietic Stem Cell Transplantation 41 0.079
36
FTL004 Fetal Erythroblastosis 20 0.079
37
P ATX002 Ataxia Telangiectasia 87 0.056
38
PLY001 Polycythemia Vera 85 0.056
39
P APL001 Aplastic Anemia 83 0.056
40
MYL040 Myelodysplastic Syndromes 81 0.056
41
c BTT002 Beta Thalassemia 78 0.056
42
LVR012 Liver Cirrhosis 77 0.056
43
ANK002 Ankylosing Spondylitis 77 0.056
44
P MYL005 Myelofibrosis 75 0.056
45
GLN003 Glanzmann's Thrombasthenia 74 0.056
46
c PRM002 Primary Hyperoxaluria 74 0.056
47
HST011 Histoplasmosis 73 0.056
48
CHR012 Chronic Granulomatous Disease 71 0.056
49
P ANG001 Angelman Syndrome 70 0.056
50
ART021 Arteriosclerosis 68 0.056
51
ATM004 Autoimmune Thrombocytopenic Purpura 68 0.056
52
c NPH012 Nephrotic Syndrome 67 0.056
53
c HMP007 Hemophilia 65 0.056
54
P BRN019 Bernard-Soulier Syndrome 65 0.056
55
ART019 Aortic Valve Stenosis 64 0.056
56
c HPT021 Hepatitis 64 0.056
57
GRY002 Gray Platelet Syndrome 63 0.056
58
HPT022 Hepatoblastoma 62 0.056
59
P CNJ013 Conjunctivitis 62 0.056
60
c ESS003 Essential Thrombocythemia 61 0.056
61
THR004 Thrombocytosis 61 0.056
62
BRN002 Bronchiolitis 61 0.056
63
BRN012 Bronchiolitis Obliterans 60 0.056
64
c PLY018 Polycythemia 59 0.056
65
CHL068 Cholestasis 59 0.056
66
MYC002 Mycobacterium Avium Complex Disease 59 0.056
67
P THR090 Thrombocythemia 1 58 0.056
68
THY033 Thyrotoxicosis 58 0.056
69
P CNG052 Congenital Amegakaryocytic Thrombocytopenia 56 0.056
70
c CHR285 Chronic Myelomonocytic Leukemia 56 0.056
71
ART001 Arterial Tortuosity Syndrome 55 0.056
72
VND002 Van Der Woude Syndrome 55 0.056
73
NPH051 Nephritis 54 0.056
74
AND003 Andersen-Tawil Syndrome 54 0.056
75
MMB002 Membranous Glomerulonephritis 53 0.056
76
HVD003 Hiv/aids 52 0.056
77
CHR005 Chorioamnionitis 50 0.056
78
P CHR092 Chronic Myeloproliferative Disease 50 0.056
79
c OPT004 Optic Atrophy 50 0.056
80
ALL009 Allergic Conjunctivitis 48 0.056
81
PRG060 Pregnancy Loss 48 0.056
82
GRN017 Granulocytopenia 47 0.056
83
RPP001 Rapp-Hodgkin Syndrome 47 0.056
84
P ART084 Arteriovenous Fistula 47 0.056
85
SPL018 Splenomegaly 47 0.056
86
PMP002 Pemphigoid Gestationis 41 0.056
87
ADS002 Adie Syndrome 35 0.056
88
FCT013 Factor V Leiden Thrombophilia 34 0.056
89
TFT003 Tufting Enteropathy 28 0.056
90
HNM002 Hinman Syndrome 28 0.056
91
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.056
92
c BNG076 Benign Exophthalmos Syndrome 22 0.056
93
RHM007 Rheumatic Congestive Heart Failure 21 0.056
94
AND005 Androgen Insensitivity Syndrome, Mild 21 0.056
95
HRD137 Hereditary Isolated Aplastic Anemia 19 0.056
96
TRN013 Transient Neonatal Thrombocytopenia 7 0.056