Search results for alloimmunization

208 hits were found for alloimmunization

# Family MCID Name MIFTS Score
1
FTL012 Fetal and Neonatal Alloimmune Thrombocytopenia 36 4.968
2
c CNG407 Congenital Membranous Nephropathy Due to Maternal Anti-Neutral Endopeptidase Alloimmunization 10 4.581
3
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 3.995
4
NNT054 Neonatal Alloimmune Neutropenia 15 3.466
5
HML043 Hemolytic Disease of the Newborn with Kell Alloimmunization 4 3.262
6
HMC038 Hemochromatosis, Neonatal 38 2.458
7
THR100 Thrombocytopenic Purpura, Autoimmune 57 2.334
8
P THR014 Thrombocytopenia 65 0.399
9
P NTR004 Neutropenia 60 0.225
10
SCK005 Sickle Cell Disease 54 0.162
11
P THL005 Thalassemia 65 0.143
12
PRP030 Purpura 61 0.114
13
SCK003 Sickle Cell Anemia 73 0.106
14
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.106
15
P HML002 Hemolytic Anemia 62 0.106
16
P LVR013 Liver Disease 76 0.097
17
HYD012 Hydrops Fetalis 50 0.097
18
THR035 Thrombasthenia 46 0.097
19
HYD059 Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect 34 0.097
20
P GRF003 Graft-Versus-Host Disease 72 0.087
21
GLN010 Glanzmann Thrombasthenia 66 0.087
22
P MMB011 Membranous Nephropathy 55 0.087
23
PNC001 Pancytopenia 50 0.087
24
HMS001 Hemosiderosis 50 0.087
25
BLD053 Blood Platelet Disease 45 0.087
26
P LKM002 Leukemia 75 0.075
27
AGN016 Aging 65 0.075
28
HMT018 Hematopoietic Stem Cell Transplantation 58 0.075
29
IMM158 Immune Suppression 57 0.075
30
c ANM038 Anemia, Autoimmune Hemolytic 56 0.075
31
END072 Endotheliitis 46 0.075
32
P HPT021 Hepatitis 75 0.061
33
APL001 Aplastic Anemia 74 0.061
34
c BTT014 Beta-Thalassemia 70 0.061
35
P MYL006 Myeloid Leukemia 69 0.061
36
c HMP029 Hemophilia a 69 0.061
37
P ANR048 Aniridia 1 68 0.061
38
c CHR417 Chronic Graft Versus Host Disease 65 0.061
39
P CHR285 Chronic Myelomonocytic Leukemia 63 0.061
40
P HMP007 Hemophilia 61 0.061
41
P GLM007 Glomerulonephritis 61 0.061
42
c ALP101 Alpha-Thalassemia 60 0.061
43
P BRN019 Bernard-Soulier Syndrome 60 0.061
44
P PRN026 Porencephaly 50 0.061
45
PLM175 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 48 0.061
46
P SDR002 Siderosis 48 0.061
47
P BLD051 Blood Coagulation Disease 38 0.061
48
P BLD124 Bleeding Disorder, Platelet-Type, 11 38 0.061
49
c BLD140 Blood Group, I System 37 0.061
50
c PRM225 Primary Thrombocytopenia 37 0.061
51
c MLT151 Multiple Mitochondrial Dysfunctions Syndrome 5 36 0.061
52
FTL004 Fetal Erythroblastosis 35 0.061
53
ATM012 Autoimmune Disease of Blood 31 0.061
54
ALR002 Al-Raqad Syndrome 30 0.061
55
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 29 0.061
56
ATS208 Autosomal Dominant Macrothrombocytopenia 27 0.061
57
ANR038 Anorexia Nervosa 1 21 0.061
58
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.061
59
BLD137 Blood Group--Ahonen 17 0.061
60
P LNG032 Lung Cancer 99 0.043
61
c SYS001 Systemic Lupus Erythematosus 86 0.043
62
P MLT020 Multiple Sclerosis 85 0.043
63
c LKM061 Leukemia, Acute Myeloid 81 0.043
64
P ART022 Arthritis 77 0.043
65
MYL009 Myelodysplastic Syndrome 75 0.043
66
ALP046 Alport Syndrome, X-Linked 74 0.043
67
PFF001 Pfeiffer Syndrome 74 0.043
68
LVR012 Liver Cirrhosis 73 0.043
69
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.043
70
VSC007 Vascular Disease 71 0.043
71
c HMC039 Hemochromatosis, Type 1 71 0.043
72
P LYM118 Lymphoma 71 0.043
73
BRC012 Brucellosis 71 0.043
74
P ESS003 Essential Thrombocythemia 71 0.043
75
P PNM007 Pneumonia 70 0.043
76
PRT037 Pertussis 70 0.043
77
P LPS004 Lupus Erythematosus 69 0.043
78
P KDN018 Kidney Disease 69 0.043
79
P CHR012 Chronic Granulomatous Disease 69 0.043
80
LNG099 Lung Disease 67 0.043
81
P CNJ013 Conjunctivitis 67 0.043
82
P PRD008 Periodontitis 67 0.043
83
ATM095 Autoimmune Disease 66 0.043
84
P ENC004 Encephalitis 66 0.043
85
c DNG003 Dengue Disease 66 0.043
86
c PRC016 Pre-Eclampsia 65 0.043
87
TTN003 Tetanus 65 0.043
88
VLC001 Velocardiofacial Syndrome 64 0.043
89
HYP066 Hyperglycemia 64 0.043
90
CRB011 Cerebrotendinous Xanthomatosis 64 0.043
91
ACT119 Acute Promyelocytic Leukemia 64 0.043
92
c HPT003 Hepatitis a 63 0.043
93
DPH001 Diphtheria 63 0.043
94
c ATM011 Autoimmune Hepatitis 63 0.043
95
c ADL017 Adult T-Cell Leukemia 63 0.043
96
P MYS005 Myositis 63 0.043
97
P THR005 Thrombotic Thrombocytopenic Purpura 63 0.043
98
INT066 Interstitial Lung Disease 63 0.043
99
P ART021 Arteriosclerosis 62 0.043
100
GST033 Gestational Diabetes 62 0.043
101
P GRV001 Graves' Disease 62 0.043
102
P ACT074 Acute Lymphocytic Leukemia 61 0.043
103
MCS002 Mucositis 61 0.043
104
VNW001 Von Willebrand's Disease 61 0.043
105
TNS005 Tonsillitis 61 0.043
106
CHL068 Cholestasis 60 0.043
107
P PLY018 Polycythemia 60 0.043
108
BRN012 Bronchiolitis Obliterans 60 0.043
109
BRN002 Bronchiolitis 59 0.043
110
P ANT006 Antiphospholipid Syndrome 59 0.043
111
LGG001 Legg-Calve-Perthes Disease 59 0.043
112
JPN002 Japanese Encephalitis 59 0.043
113
RLP002 Relapsing-Remitting Multiple Sclerosis 59 0.043
114
THR009 Thrombocytopenia-Absent Radius Syndrome 58 0.043
115
LYM040 Lymphoblastic Lymphoma 58 0.043
116
P THR015 Thrombophilia 58 0.043
117
URN009 Urinary System Disease 58 0.043
118
P ECL001 Eclampsia 57 0.043
119
P LPD010 Lipodystrophy 57 0.043
120
VND007 Van Der Woude Syndrome 1 57 0.043
121
SPT005 Spotted Fever 57 0.043
122
INF034 Infective Endocarditis 56 0.043
123
HST011 Histoplasmosis 56 0.043
124
P THY032 Thyroiditis 56 0.043
125
GRY002 Gray Platelet Syndrome 56 0.043
126
THR004 Thrombocytosis 55 0.043
127
P SYP003 Syphilis 55 0.043
128
INT007 Intermediate Coronary Syndrome 55 0.043
129
P TRC086 Trichohepatoenteric Syndrome 1 54 0.043
130
MCR004 Macroglobulinemia 54 0.043
131
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 54 0.043
132
ALL009 Allergic Conjunctivitis 53 0.043
133
XNT003 Xanthomatosis 53 0.043
134
RNP003 Renpenning Syndrome 1 53 0.043
135
HMG005 Hemoglobinopathy 53 0.043
136
HPT082 Hepatic Adenomas, Familial 52 0.043
137
CHR005 Chorioamnionitis 52 0.043
138
PRR002 Pure Red-Cell Aplasia 52 0.043
139
c GRV008 Graves Disease 1 52 0.043
140
c AMG001 Amegakaryocytic Thrombocytopenia, Congenital 51 0.043
141
BBS001 Babesiosis 51 0.043
142
c ACQ014 Acquired Hemophilia 51 0.043
143
CLD007 Cold Agglutinin Disease 50 0.043
144
P MRC003 Mercury Poisoning 50 0.043
145
P TCL004 T-Cell Leukemia 50 0.043
146
THR013 Thoracic Outlet Syndrome 50 0.043
147
c ART119 Arthrogryposis, Distal, Type 5 49 0.043
148
MTC056 Mitochondrial Dna Depletion Syndrome 4a 49 0.043
149
AND020 Androgen Insensitivity, Partial 49 0.043
150
GRN017 Granulocytopenia 49 0.043
151
HPR003 Heparin-Induced Thrombocytopenia 48 0.043
152
P PLM085 Pulmonary Hemosiderosis 48 0.043
153
HNC001 Henoch-Schoenlein Purpura 48 0.043
154
BSC001 Buschke-Ollendorff Syndrome 48 0.043
155
ISC002 Ischemic Optic Neuropathy 48 0.043
156
PLC008 Placenta Disease 48 0.043
157
CRN017 Coronary Thrombosis 48 0.043
158
LKC005 Leukocyte Adhesion Deficiency, Type Iii 47 0.043
159
PTT041 Pituitary Stalk Interruption Syndrome 47 0.043
160
PTT004 Pituitary Apoplexy 47 0.043
161
EHR002 Ehrlichiosis 45 0.043
162
P ACQ022 Acquired Generalized Lipodystrophy 45 0.043
163
c ACQ042 Acquired Hemophilia a 44 0.043
164
RTR011 Retroperitoneal Fibrosis 43 0.043
165
RCK002 Rocky Mountain Spotted Fever 42 0.043
166
SPL012 Splenic Disease 42 0.043
167
EXN001 Exanthema Subitum 42 0.043
168
c HMC010 Hemochromatosis, Type 3 42 0.043
169
GLC106 Glucocorticoid Resistance, Generalized 41 0.043
170
c ALZ056 Alzheimer Disease 3 41 0.043
171
ADP007 Adie Pupil 41 0.043
172
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 41 0.043
173
MYH012 Myhre Syndrome 41 0.043
174
P PRC031 Preeclampsia/eclampsia 1 41 0.043
175
c CNG033 Congenital Syphilis 40 0.043
176
LYM010 Lymph Node Tuberculosis 40 0.043
177
PMP002 Pemphigoid Gestationis 40 0.043
178
CPL005 Capillary Disease 38 0.043
179
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 38 0.043
180
CRT004 Carotid Artery Thrombosis 37 0.043
181
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.043
182
c THR090 Thrombocythemia 1 37 0.043
183
P ANX007 Anauxetic Dysplasia 1 36 0.043
184
ANG037 Angiomatosis 36 0.043
185
PRC005 Pericardial Tuberculosis 35 0.043
186
ASY002 Asymptomatic Neurosyphilis 34 0.043
187
c BLD152 Bleeding Disorder, Platelet-Type, 16 34 0.043
188
c DYS174 Dyskeratosis Congenita, Autosomal Dominant 6 34 0.043
189
MNG003 Mungan Syndrome 34 0.043
190
SCL025 Scleromyxedema 34 0.043
191
ACT118 Acute Non Lymphoblastic Leukemia 32 0.043
192
c PRM022 Primary Syphilis 32 0.043
193
c THR111 Thrombocytopenia 3 32 0.043
194
ART110 Arteritic Anterior Ischemic Optic Neuropathy 31 0.043
195
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.043
196
c SRC023 Sarcoidosis 2 30 0.043
197
c INH004 Inherited Blood Coagulation Disease 29 0.043
198
TRT002 Tertiary Neurosyphilis 29 0.043
199
LTN001 Latent Syphilis 29 0.043
200
TRT003 Tertiary Syphilis 29 0.043
201
BLD052 Blood Group Incompatibility 26 0.043
202
c ERL002 Early Congenital Syphilis 24 0.043
203
BLD163 Blood Group, Dombrock System 23 0.043
204
MXD035 Mixed-Type Autoimmune Hemolytic Anemia 22 0.043
205
TRN017 Transient Neonatal Neutropenia 19 0.043
206
IMM162 Immunoglobulin E Concentration, Serum 16 0.043
207
LRY021 Laryngeal Adductor Paralysis 15 0.043
208
TRN013 Transient Neonatal Thrombocytopenia 11 0.043
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