Search results for "alloimmunization"

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

95 hits were found for 'alloimmunization'

# Family MCID Name MIFTS Score
1
FTL012 Fetal and Neonatal Alloimmune Thrombocytopenia 34 4.781
2
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 21 4.600
3
CNG407 Congenital Membranous Nephropathy Due to Maternal Anti-Neutral Endopeptidase Alloimmunization 8 4.600
4
NTR014 Neutropenia, Alloimmune Neonatal 8 3.984
5
HML043 Hemolytic Disease of the Newborn with Kell Alloimmunization 4 3.984
6
THR095 Thrombocytopenia, Neonatal Alloimmune 8 3.370
7
THR094 Thrombocytopenia, Neonatal Alloimmune, Bak Antigen Related 5 3.253
8
c THR014 Thrombocytopenia 69 0.378
9
c NTR004 Neutropenia 65 0.218
10
c NNT047 Neonatal Neutropenia 28 0.195
11
SCK005 Sickle Cell Disease 61 0.169
12
NNT016 Neonatal Hemochromatosis 49 0.149
13
PRP030 Purpura 65 0.138
14
c HML002 Hemolytic Anemia 65 0.126
15
HYD012 Hydrops Fetalis 61 0.126
16
P HMC003 Hemochromatosis 85 0.113
17
SCK003 Sickle Cell Anemia 84 0.113
18
c THL005 Thalassemia 71 0.113
19
P LVR013 Liver Disease 68 0.113
20
P GRF002 Graft Versus Host Disease 64 0.113
21
THR013 Thoracic Outlet Syndrome 52 0.113
22
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 43 0.113
23
P ATM010 Autoimmune Hemolytic Anemia 66 0.098
24
END072 Endotheliitis 50 0.098
25
THR035 Thrombasthenia 44 0.098
26
SYN053 Syndromic Diarrhea 34 0.098
27
AND002 Androgen Insensitivity Syndrome 80 0.080
28
P LKM002 Leukemia 76 0.080
29
P ALP006 Alpha Thalassemia 74 0.080
30
c AXN002 Axenfeld-Rieger Syndrome 69 0.080
31
P SDR002 Siderosis 57 0.080
32
P PNC001 Pancytopenia 48 0.080
33
c PRN026 Porencephaly 47 0.080
34
c CHR417 Chronic Graft Versus Host Disease 42 0.080
35
HMT018 Hematopoietic Stem Cell Transplantation 40 0.080
36
FTL004 Fetal Erythroblastosis 19 0.080
37
P ATX002 Ataxia Telangiectasia 87 0.056
38
PLY001 Polycythemia Vera 85 0.056
39
P APL001 Aplastic Anemia 84 0.056
40
c BTT002 Beta Thalassemia 82 0.056
41
MYL040 Myelodysplastic Syndromes 79 0.056
42
GLN003 Glanzmann's Thrombasthenia 76 0.056
43
LVR012 Liver Cirrhosis 76 0.056
44
ANK002 Ankylosing Spondylitis 76 0.056
45
CHR012 Chronic Granulomatous Disease 74 0.056
46
P MYL005 Myelofibrosis 74 0.056
47
HST011 Histoplasmosis 73 0.056
48
c PRM002 Primary Hyperoxaluria 73 0.056
49
P ANG001 Angelman Syndrome 71 0.056
50
ATM004 Autoimmune Thrombocytopenic Purpura 69 0.056
51
ART021 Arteriosclerosis 67 0.056
52
c NPH012 Nephrotic Syndrome 67 0.056
53
c HMP007 Hemophilia 64 0.056
54
P BRN019 Bernard-Soulier Syndrome 64 0.056
55
ART019 Aortic Valve Stenosis 63 0.056
56
c HPT021 Hepatitis 63 0.056
57
GRY002 Gray Platelet Syndrome 63 0.056
58
P CNJ013 Conjunctivitis 61 0.056
59
c ESS003 Essential Thrombocythemia 61 0.056
60
THR004 Thrombocytosis 60 0.056
61
BRN002 Bronchiolitis 60 0.056
62
BRN012 Bronchiolitis Obliterans 59 0.056
63
c PLY018 Polycythemia 59 0.056
64
P THR090 Thrombocythemia 1 58 0.056
65
CHL068 Cholestasis 58 0.056
66
MYC002 Mycobacterium Avium Complex Disease 58 0.056
67
THY033 Thyrotoxicosis 57 0.056
68
P CNG052 Congenital Amegakaryocytic Thrombocytopenia 56 0.056
69
ART001 Arterial Tortuosity Syndrome 55 0.056
70
VND002 Van Der Woude Syndrome 55 0.056
71
c CHR285 Chronic Myelomonocytic Leukemia 55 0.056
72
NPH051 Nephritis 53 0.056
73
AND003 Andersen-Tawil Syndrome 53 0.056
74
MMB002 Membranous Glomerulonephritis 52 0.056
75
HVD003 Hiv/aids 51 0.056
76
RPP001 Rapp-Hodgkin Syndrome 50 0.056
77
CHR005 Chorioamnionitis 50 0.056
78
P CHR092 Chronic Myeloproliferative Disease 49 0.056
79
c OPT004 Optic Atrophy 49 0.056
80
ALL009 Allergic Conjunctivitis 47 0.056
81
PRG060 Pregnancy Loss 47 0.056
82
GRN017 Granulocytopenia 46 0.056
83
P ART084 Arteriovenous Fistula 46 0.056
84
SPL018 Splenomegaly 46 0.056
85
PMP002 Pemphigoid Gestationis 41 0.056
86
ADS002 Adie Syndrome 35 0.056
87
FCT013 Factor V Leiden Thrombophilia 34 0.056
88
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 29 0.056
89
HNM002 Hinman Syndrome 28 0.056
90
TFT003 Tufting Enteropathy 28 0.056
91
c BNG076 Benign Exophthalmos Syndrome 22 0.056
92
RHM007 Rheumatic Congestive Heart Failure 21 0.056
93
AND005 Androgen Insensitivity Syndrome, Mild 21 0.056
94
HRD137 Hereditary Isolated Aplastic Anemia 20 0.056
95
TRN013 Transient Neonatal Thrombocytopenia 7 0.056