Search results for "alloimmunization"

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

132 hits were found for 'alloimmunization'

# Family MCID Name MIFTS Score
1
FTL012 Fetal and Neonatal Alloimmune Thrombocytopenia 31 4.388
2
THR095 Thrombocytopenia, Neonatal Alloimmune 13 4.093
3
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 44 4.041
4
c CNG407 Congenital Membranous Nephropathy Due to Maternal Anti-Neutral Endopeptidase Alloimmunization 9 4.000
5
NTR014 Neutropenia, Alloimmune Neonatal 7 4.000
6
HML043 Hemolytic Disease of the Newborn with Kell Alloimmunization 4 3.283
7
THR100 Thrombocytopenic Purpura, Autoimmune 53 2.322
8
P THR014 Thrombocytopenia 64 0.433
9
P NTR004 Neutropenia 59 0.195
10
SCK005 Sickle Cell Disease 49 0.175
11
P THL005 Thalassemia 61 0.151
12
P HMC003 Hemochromatosis 72 0.123
13
PRP030 Purpura 59 0.123
14
P LVR013 Liver Disease 72 0.113
15
P HML002 Hemolytic Anemia 60 0.113
16
HYD012 Hydrops Fetalis 44 0.113
17
SCK003 Sickle Cell Anemia 68 0.101
18
P MMB011 Membranous Nephropathy 56 0.101
19
THL018 Thalassemia Major 42 0.101
20
HMC038 Hemochromatosis, Neonatal 27 0.101
21
c ATM010 Autoimmune Hemolytic Anemia 60 0.087
22
BLD053 Blood Platelet Disease 46 0.087
23
TNP003 Tn Polyagglutination Syndrome, Somatic 44 0.087
24
END072 Endotheliitis 42 0.087
25
THR035 Thrombasthenia 42 0.087
26
ALR002 Al-Raqad Syndrome 36 0.087
27
GLN010 Glanzmann Thrombasthenia 63 0.071
28
P GLM007 Glomerulonephritis 56 0.071
29
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.071
30
P PNC001 Pancytopenia 52 0.071
31
c CHR417 Chronic Graft Versus Host Disease 50 0.071
32
P PRN026 Porencephaly 47 0.071
33
ACR041 Acromelic Frontonasal Dysostosis 46 0.071
34
P SDR002 Siderosis 44 0.071
35
BRT030 Birth Defects 43 0.071
36
c PRM225 Primary Thrombocytopenia 42 0.071
37
HMT018 Hematopoietic Stem Cell Transplantation 41 0.071
38
c THR037 Thrombocytopenia 2 37 0.071
39
CCN007 Cocoon Syndrome 35 0.071
40
FTL004 Fetal Erythroblastosis 35 0.071
41
BLD052 Blood Group Incompatibility 28 0.071
42
MYL009 Myelodysplastic Syndrome 74 0.050
43
P APL001 Aplastic Anemia 73 0.050
44
c LKM061 Leukemia, Acute Myeloid 71 0.050
45
P HPT021 Hepatitis 70 0.050
46
P LKM002 Leukemia 70 0.050
47
P MYL006 Myeloid Leukemia 67 0.050
48
VSC007 Vascular Disease 67 0.050
49
LVR012 Liver Cirrhosis 67 0.050
50
CHR012 Chronic Granulomatous Disease 65 0.050
51
DFC004 Deficiency Anemia 65 0.050
52
P CNJ013 Conjunctivitis 65 0.050
53
c HMP029 Hemophilia a 64 0.050
54
HMT002 Hematologic Cancer 64 0.050
55
c ACT073 Acute Leukemia 62 0.050
56
HYP066 Hyperglycemia 60 0.050
57
ART021 Arteriosclerosis 59 0.050
58
CHL068 Cholestasis 58 0.050
59
BRN012 Bronchiolitis Obliterans 58 0.050
60
P PRC031 Preeclampsia/eclampsia 1 57 0.050
61
GST033 Gestational Diabetes 56 0.050
62
BRN002 Bronchiolitis 56 0.050
63
P HMP007 Hemophilia 56 0.050
64
CHR285 Chronic Myelomonocytic Leukemia 55 0.050
65
P ECL001 Eclampsia 54 0.050
66
HST011 Histoplasmosis 54 0.050
67
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 53 0.050
68
P RNL028 Renal Tubular Dysgenesis 52 0.050
69
ALL009 Allergic Conjunctivitis 51 0.050
70
VND002 Van Der Woude Syndrome 51 0.050
71
IMP005 Impotence 50 0.050
72
HRT007 Heart Cancer 50 0.050
73
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 49 0.050
74
P PNV001 Panuveitis 49 0.050
75
ACT049 Acute Disseminated Encephalomyelitis 49 0.050
76
THR013 Thoracic Outlet Syndrome 49 0.050
77
c INH020 Inherited Metabolic Disorder 49 0.050
78
ACT017 Acute Chest Syndrome 48 0.050
79
CHR005 Chorioamnionitis 48 0.050
80
WHP001 Whipple Disease 48 0.050
81
SXL003 Sexual Disorder 47 0.050
82
P RNV001 Renovascular Hypertension 47 0.050
83
MCR191 Microscopic Colitis 47 0.050
84
P TRC086 Trichohepatoenteric Syndrome 1 46 0.050
85
c ATM024 Autoimmune Pancreatitis 46 0.050
86
CRB004 Cerebral Artery Occlusion 46 0.050
87
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 45 0.050
88
DFF035 Diffuse Cutaneous Systemic Sclerosis 45 0.050
89
IDP024 Idiopathic Inflammatory Myopathy 45 0.050
90
PNT038 Peanut Allergy 44 0.050
91
GGR001 Geographic Tongue 44 0.050
92
CRV043 Cervical Dystonia 44 0.050
93
c CHR064 Chronic Monocytic Leukemia 43 0.050
94
RHM014 Rheumatoid Vasculitis 43 0.050
95
IRN002 Iron Metabolism Disease 43 0.050
96
CRN019 Coronary Artery Vasospasm 42 0.050
97
ART031 Aortic Coarctation 42 0.050
98
LCH009 Lichen Sclerosus 42 0.050
99
GRN017 Granulocytopenia 42 0.050
100
c CHR546 Chronic Mountain Sickness 42 0.050
101
PTY001 Pityriasis Rosea 41 0.050
102
c CHR576 Chronic Beryllium Disease 41 0.050
103
RCR004 Recurrent Respiratory Papillomatosis 40 0.050
104
CPL005 Capillary Disease 40 0.050
105
P HYP263 Hypersomnia 40 0.050
106
PRN037 Prinzmetal's Variant Angina 40 0.050
107
TTR005 Tetrahydrobiopterin Deficiency 40 0.050
108
BLD054 Blood Protein Disease 40 0.050
109
THL017 Thalassemia Intermedia 40 0.050
110
PRS030 Persistent Fetal Circulation Syndrome 40 0.050
111
c HMC010 Hemochromatosis, Type 3 38 0.050
112
P BRY005 Beryllium Disease 38 0.050
113
MTL002 Metal Metabolism Disorder 38 0.050
114
LCH011 Lichen Planopilaris 37 0.050
115
OST115 Osteonecrosis of the Jaw 37 0.050
116
ATM012 Autoimmune Disease of Blood 37 0.050
117
IDP074 Idiopathic Bronchiectasis 37 0.050
118
PDC001 Podoconiosis 36 0.050
119
PLC008 Placenta Disease 36 0.050
120
P HRT017 Heart Tumor 35 0.050
121
NNT011 Neonatal Anemia 34 0.050
122
MTL005 Metal Allergy 34 0.050
123
c TYP024 Type Ii Mixed Cryoglobulinemia 34 0.050
124
PMP002 Pemphigoid Gestationis 34 0.050
125
P ACT080 Acute Pulmonary Heart Disease 32 0.050
126
c MLG080 Malignant Secondary Hypertension 30 0.050
127
ACT118 Acute Non Lymphoblastic Leukemia 29 0.050
128
ACH015 Achalasia, Familial Esophageal 28 0.050
129
c ADL079 Adult Heart Tumor 19 0.050
130
TRN017 Transient Neonatal Neutropenia 18 0.050
131
HRT029 Heart Tumor of the Child 17 0.050
132
TRN013 Transient Neonatal Thrombocytopenia 14 0.050