Search results for "alloimmunization"

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

180 hits were found for 'alloimmunization'

# Family MCID Name MIFTS Score
1
FTL012 Fetal and Neonatal Alloimmune Thrombocytopenia 32 4.344
2
THR095 Thrombocytopenia, Neonatal Alloimmune 13 4.040
3
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 4.023
4
c CNG407 Congenital Membranous Nephropathy Due to Maternal Anti-Neutral Endopeptidase Alloimmunization 9 3.986
5
NTR014 Neutropenia, Alloimmune Neonatal 7 3.986
6
HML043 Hemolytic Disease of the Newborn with Kell Alloimmunization 4 3.270
7
THR100 Thrombocytopenic Purpura, Autoimmune 54 2.312
8
P THR014 Thrombocytopenia 64 0.392
9
P NTR004 Neutropenia 59 0.176
10
SCK005 Sickle Cell Disease 51 0.151
11
P THL005 Thalassemia 64 0.144
12
P HMC003 Hemochromatosis 72 0.111
13
P HML002 Hemolytic Anemia 62 0.111
14
PRP030 Purpura 58 0.111
15
HYD012 Hydrops Fetalis 43 0.111
16
P LVR013 Liver Disease 75 0.102
17
SCK003 Sickle Cell Anemia 71 0.091
18
P MMB011 Membranous Nephropathy 54 0.091
19
THL018 Thalassemia Major 48 0.091
20
HMC038 Hemochromatosis, Neonatal 29 0.091
21
c ATM010 Autoimmune Hemolytic Anemia 61 0.079
22
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.079
23
BLD053 Blood Platelet Disease 46 0.079
24
CCN007 Cocoon Syndrome 45 0.079
25
END072 Endotheliitis 42 0.079
26
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.079
27
THR035 Thrombasthenia 39 0.079
28
ALR002 Al-Raqad Syndrome 36 0.079
29
FTL004 Fetal Erythroblastosis 33 0.079
30
DFC004 Deficiency Anemia 64 0.064
31
GLN010 Glanzmann Thrombasthenia 63 0.064
32
P GLM007 Glomerulonephritis 59 0.064
33
P PNC001 Pancytopenia 52 0.064
34
c CHR417 Chronic Graft Versus Host Disease 51 0.064
35
THR013 Thoracic Outlet Syndrome 50 0.064
36
P PRN026 Porencephaly 48 0.064
37
ACR041 Acromelic Frontonasal Dysostosis 45 0.064
38
P SDR002 Siderosis 44 0.064
39
BRT030 Birth Defects 43 0.064
40
HMT018 Hematopoietic Stem Cell Transplantation 41 0.064
41
c PRM225 Primary Thrombocytopenia 39 0.064
42
c THR037 Thrombocytopenia 2 35 0.064
43
NNT011 Neonatal Anemia 33 0.064
44
PLC008 Placenta Disease 33 0.064
45
BLD052 Blood Group Incompatibility 27 0.064
46
P APL001 Aplastic Anemia 75 0.046
47
c LKM061 Leukemia, Acute Myeloid 73 0.046
48
MYL009 Myelodysplastic Syndrome 73 0.046
49
P LKM002 Leukemia 71 0.046
50
P HPT021 Hepatitis 69 0.046
51
P DRV001 Dravet Syndrome 69 0.046
52
LVR012 Liver Cirrhosis 67 0.046
53
P KDN018 Kidney Disease 66 0.046
54
P EPL164 Epilepsy 66 0.046
55
P MYL006 Myeloid Leukemia 66 0.046
56
CHR012 Chronic Granulomatous Disease 65 0.046
57
P CNJ013 Conjunctivitis 64 0.046
58
HMT002 Hematologic Cancer 64 0.046
59
c HMP029 Hemophilia a 63 0.046
60
HYP066 Hyperglycemia 61 0.046
61
c ACT073 Acute Leukemia 60 0.046
62
P ENC018 Encephalopathy 59 0.046
63
STT001 Status Epilepticus 59 0.046
64
CHL068 Cholestasis 59 0.046
65
ART021 Arteriosclerosis 58 0.046
66
BRN012 Bronchiolitis Obliterans 58 0.046
67
P HMP007 Hemophilia 57 0.046
68
GST033 Gestational Diabetes 57 0.046
69
c PRC016 Pre-Eclampsia 56 0.046
70
BRN002 Bronchiolitis 56 0.046
71
CHR285 Chronic Myelomonocytic Leukemia 56 0.046
72
MCS002 Mucositis 55 0.046
73
ESP023 Esophageal Disease 54 0.046
74
P ECL001 Eclampsia 54 0.046
75
THL016 Thalassemias, Alpha- 53 0.046
76
HMG005 Hemoglobinopathy 52 0.046
77
HST011 Histoplasmosis 52 0.046
78
P PRC031 Preeclampsia/eclampsia 1 51 0.046
79
ALL009 Allergic Conjunctivitis 51 0.046
80
P RNL028 Renal Tubular Dysgenesis 51 0.046
81
VND002 Van Der Woude Syndrome 50 0.046
82
NNT012 Neonatal Jaundice 50 0.046
83
HPT074 Hepatic Adenoma, Somatic 50 0.046
84
c INH020 Inherited Metabolic Disorder 49 0.046
85
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 48 0.046
86
RPP001 Rapp-Hodgkin Syndrome 48 0.046
87
CHR005 Chorioamnionitis 48 0.046
88
P TRC086 Trichohepatoenteric Syndrome 1 48 0.046
89
c HMG001 Hemoglobin C Disease 47 0.046
90
HMS001 Hemosiderosis 46 0.046
91
HRT007 Heart Cancer 46 0.046
92
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 46 0.046
93
P INF016 Infantile Epileptic Encephalopathy 46 0.046
94
INC022 Inclusion-Cell Disease 46 0.046
95
P KRN004 Kernicterus 46 0.046
96
GRN017 Granulocytopenia 44 0.046
97
c HMG003 Hemoglobin E Disease 44 0.046
98
ECT093 Ectopic Cushing Syndrome 43 0.046
99
DRR008 Diarrhea 1, Secretory Chloride, Congenital 42 0.046
100
BLR008 Bilirubin Metabolic Disorder 42 0.046
101
c CHR064 Chronic Monocytic Leukemia 42 0.046
102
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.046
103
SPR007 Superior Mesenteric Artery Syndrome 41 0.046
104
IRN002 Iron Metabolism Disease 41 0.046
105
ESP025 Esophagus Adenocarcinoma 41 0.046
106
ESN004 Eosinophilic Gastritis 41 0.046
107
THL017 Thalassemia Intermedia 40 0.046
108
c SCN005 Secondary Hypertrophic Osteoarthropathy 40 0.046
109
EXN001 Exanthema Subitum 39 0.046
110
c HMC010 Hemochromatosis, Type 3 39 0.046
111
TTZ003 Tietz Albinism-Deafness Syndrome 39 0.046
112
c EPL029 Epileptic Encephalopathy, Early Infantile, 9 39 0.046
113
MYH012 Myhre Syndrome 38 0.046
114
BLD054 Blood Protein Disease 37 0.046
115
SHW001 Shwartzman Phenomenon 37 0.046
116
MYP100 Myopathy, X-Linked, with Excessive Autophagy 37 0.046
117
BNS002 Bone Structure Disease 37 0.046
118
CPL005 Capillary Disease 36 0.046
119
IMM003 Immunoglobulin Alpha Deficiency 36 0.046
120
KLN009 Kleine-Levin Hibernation Syndrome 36 0.046
121
NTR005 Nutritional Deficiency Disease 36 0.046
122
PRC005 Pericardial Tuberculosis 36 0.046
123
MTL002 Metal Metabolism Disorder 35 0.046
124
ATM012 Autoimmune Disease of Blood 35 0.046
125
PMP002 Pemphigoid Gestationis 35 0.046
126
ADP007 Adie Pupil 34 0.046
127
PNC028 Pancreatic Steatorrhea 34 0.046
128
PLY131 Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes 34 0.046
129
CNG436 Congenital Disorder of Deglycosylation 34 0.046
130
RMN001 Rumination Disorder 34 0.046
131
LRY017 Laryngeal Disease 34 0.046
132
P TST001 Testicular Leydig Cell Tumor 33 0.046
133
IMM039 Immune Hydrops Fetalis 33 0.046
134
GLS004 Glossopharyngeal Neuralgia 33 0.046
135
FNC006 Functional Gastric Disease 32 0.046
136
NRD001 Neurodermatitis 32 0.046
137
P HRT017 Heart Tumor 32 0.046
138
CLC011 Cloacal Exstrophy 32 0.046
139
CLN006 Colonic Pseudo-Obstruction 31 0.046
140
P ACT080 Acute Pulmonary Heart Disease 31 0.046
141
c CHR057 Chronic Laryngitis 31 0.046
142
ALB003 Albinism-Deafness Syndrome 30 0.046
143
NNT005 Neonatal Candidiasis 30 0.046
144
c ACT072 Acute Laryngitis 30 0.046
145
ACT118 Acute Non Lymphoblastic Leukemia 30 0.046
146
GST004 Gastric Neuroendocrine Neoplasm 30 0.046
147
ISC001 Ischemic Neuropathy 30 0.046
148
BLD041 Bladder Calculus 30 0.046
149
MRG013 Mirage Syndrome 29 0.046
150
PNM003 Pneumatosis Cystoides Intestinalis 29 0.046
151
PHT004 Photoallergic Dermatitis 28 0.046
152
SQM005 Squamous Papillomatosis 28 0.046
153
LRY007 Laryngeal Tuberculosis 28 0.046
154
DNT046 Dental Abscess 28 0.046
155
LWR004 Lower Urinary Tract Calculus 28 0.046
156
RHS001 Rh Isoimmunization 28 0.046
157
GRN011 Granulomatous Gastritis 28 0.046
158
THY001 Thyroid Crisis 27 0.046
159
FNG003 Fungal Esophagitis 27 0.046
160
OCL003 Oculomotor Nerve Paralysis 27 0.046
161
FNC005 Functional Colonic Disease 27 0.046
162
ANS018 Anismus 27 0.046
163
HMD003 Hemidystonia 26 0.046
164
VSL003 Visual Agnosia 26 0.046
165
CHR067 Chronic Intestinal Vascular Insufficiency 26 0.046
166
THR010 Third Cranial Nerve Disease 26 0.046
167
HNM002 Hinman Syndrome 25 0.046
168
GST090 Gastroduodenal Crohn's Disease 25 0.046
169
FBR064 Febrile Infection-Related Epilepsy Syndrome 25 0.046
170
IMM025 Immunoglobulin a Deficiency 2 24 0.046
171
c GST091 Gastrointestinal Neuroendocrine Benign Tumor 24 0.046
172
INF033 Infancy Electroclinical Syndrome 21 0.046
173
ADT001 Auditory Agnosia 20 0.046
174
TRN017 Transient Neonatal Neutropenia 18 0.046
175
c ADL079 Adult Heart Tumor 16 0.046
176
AND005 Androgen Insensitivity Syndrome, Mild 16 0.046
177
FTL016 Fetal Edema 15 0.046
178
HRT029 Heart Tumor of the Child 15 0.046
179
TRN013 Transient Neonatal Thrombocytopenia 13 0.046
180
c KRN003 Kernicterus Due to Isoimmunization 12 0.046