Search results for "eosinophilic myeloproliferative disorder"

The MalaCard for "eosinophilic myeloproliferative disorder" has been retired.
Searching MalaCards for entries containing "eosinophilic myeloproliferative disorder"

200 hits were found for 'eosinophilic myeloproliferative disorder'

# Family MCID Name MIFTS Score
1
MYL015 Myeloproliferative Disorder with Eosinophilia 34 5.989
2
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 17 4.203
3
P LKM002 Leukemia 70 0.430
4
P ESP024 Esophagitis 62 0.374
5
P ESN007 Eosinophilia 61 0.334
6
P AST005 Asthma 80 0.306
7
TNP003 Tn Polyagglutination Syndrome, Somatic 30 0.266
8
BNM001 Bone Marrow Cancer 56 0.259
9
c CHR092 Chronic Myeloproliferative Disease 50 0.254
10
P HYP098 Hypereosinophilic Syndrome 48 0.223
11
P LYM118 Lymphoma 68 0.218
12
P MYL005 Myelofibrosis 67 0.218
13
P MNN013 Meningitis 66 0.216
14
P MYL006 Myeloid Leukemia 67 0.211
15
LKC003 Leukocyte Disease 45 0.210
16
MYL009 Myelodysplastic Syndrome 73 0.208
17
THR004 Thrombocytosis 55 0.208
18
SPN041 Spinal Cord Disease 50 0.207
19
ESN006 Eosinophilic Meningitis 34 0.206
20
DWN001 Down Syndrome 65 0.199
21
P PLY018 Polycythemia 58 0.188
22
BNS002 Bone Structure Disease 37 0.187
23
CHR563 Chronic Eosinophilic Leukemia 46 0.186
24
END072 Endotheliitis 41 0.182
25
WLL006 Wells Syndrome 57 0.178
26
ALR002 Al-Raqad Syndrome 36 0.167
27
c ACT073 Acute Leukemia 61 0.165
28
MYL004 Myelodysplastic Myeloproliferative Cancer 46 0.164
29
HMT002 Hematologic Cancer 62 0.163
30
P HPT021 Hepatitis 74 0.160
31
c CHR285 Chronic Myelomonocytic Leukemia 54 0.154
32
DRM006 Dermatitis 58 0.153
33
P ACT117 Acute Myelomonocytic Leukemia 46 0.148
34
c CHR418 Chronic Leukemia 48 0.146
35
GST078 Gastrointestinal Allergy 41 0.144
36
P LKM068 Leukemia, Chronic Myeloid, Somatic 65 0.141
37
P ATP001 Atopic Dermatitis 60 0.136
38
C3D001 C3 Deficiency 50 0.135
39
ALL026 Allergic Hypersensitivity Disease 53 0.134
40
P MST009 Mastocytosis 54 0.134
41
BLD053 Blood Platelet Disease 44 0.133
42
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 34 0.132
43
c LKM061 Leukemia, Acute Myeloid 71 0.131
44
VSC011 Vasculitis 62 0.130
45
ACD009 Acid-Labile Subunit, Deficiency of 37 0.128
46
P LYM026 Lymphoblastic Leukemia 60 0.128
47
LNG099 Lung Disease 63 0.125
48
INC022 Inclusion-Cell Disease 46 0.125
49
LKM001 Leukemoid Reaction 46 0.123
50
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.122
51
CRB009 Cerebritis 36 0.120
52
PHY002 Physical Disorder 43 0.120
53
LRN003 Learning Disability 49 0.119
54
RSP006 Respiratory System Disease 61 0.118
55
ATN002 Autonomic Nervous System Disease 46 0.118
56
MTH009 Mouth Disease 63 0.115
57
ADL002 Adult Syndrome 53 0.114
58
CHL071 Child Syndrome 58 0.114
59
KDS001 Kid Syndrome 53 0.113
60
c SYS004 Systemic Mastocytosis 60 0.112
61
CSY001 C Syndrome 49 0.112
62
BLD054 Blood Protein Disease 38 0.111
63
ALN001 Aland Island Eye Disease 45 0.110
64
c AST039 Asthma 2 28 0.110
65
PLM035 Pulmonary Eosinophilia 46 0.108
66
P MYS005 Myositis 57 0.107
67
DSS003 Disseminated Eosinophilic Collagen Disease 17 0.106
68
PDG001 Pdgfra-Associated Chronic Eosinophilic Leukemia 15 0.106
69
LYM040 Lymphoblastic Lymphoma 51 0.104
70
P MYP004 Myopathy 67 0.103
71
BRT030 Birth Defects 44 0.101
72
ACR041 Acromelic Frontonasal Dysostosis 45 0.100
73
SKN016 Skin Disease 69 0.099
74
CNN005 Connective Tissue Disease 60 0.099
75
PRP019 Peripheral Nervous System Disease 52 0.097
76
P SPS003 Spastic Diplegia 49 0.096
77
PHY001 Physiological Polycythemia 31 0.095
78
RFR010 Refractory Anemia 43 0.093
79
c PRM149 Primary Hypereosinophilic Syndrome 39 0.090
80
P ENC018 Encephalopathy 59 0.089
81
SPL018 Splenomegaly 45 0.088
82
SRC014 Sarcoma 66 0.088
83
P CRD011 Cardiomyopathy 66 0.087
84
GRF001 Graft-Versus-Host Disease, Protection Against 54 0.087
85
LYM024 Lymphatic System Disease 49 0.086
86
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 36 0.084
87
PRT036 Peritonitis 65 0.084
88
c ACT020 Acute T Cell Leukemia 38 0.084
89
HMT018 Hematopoietic Stem Cell Transplantation 39 0.084
90
ADJ001 Adjustment Disorder 38 0.083
91
MYL052 Myeloproliferative Neoplasms, Familial 16 0.083
92
WTH001 Withdrawal Disorder 36 0.082
93
P MSC033 Muscle Disorders 52 0.081
94
P THR014 Thrombocytopenia 63 0.080
95
P MNC007 Monocytic Leukemia 52 0.079
96
P LVR013 Liver Disease 76 0.079
97
P MYL007 Myeloma 52 0.079
98
P ACT135 Acute Graft Versus Host Disease 52 0.078
99
P HML002 Hemolytic Anemia 60 0.078
100
VSC007 Vascular Disease 51 0.077
101
NTR005 Nutritional Deficiency Disease 51 0.077
102
c ADL001 Adult Lymphoma 40 0.077
103
c CLD010 Cold-Induced Sweating Syndrome 1 43 0.077
104
P PRT013 Portal Hypertension 61 0.077
105
P BRS047 Breast Cancer 100 0.077
106
TBR010 Tuberculosis 70 0.076
107
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.075
108
SKN027 Skin Conditions 44 0.074
109
MSC004 Muscle Tissue Disease 35 0.074
110
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 59 0.074
111
ORL011 Oral Cancer 53 0.074
112
SPC003 Specific Developmental Disorder 39 0.073
113
P PLM036 Pulmonary Fibrosis 69 0.073
114
MST017 Mast Cell Disease 52 0.073
115
c CHR417 Chronic Graft Versus Host Disease 50 0.073
116
HDG012 Hodgkin Lymphoma 75 0.073
117
PNN001 Panniculitis 47 0.073
118
UPP004 Upper Respiratory Tract Disease 48 0.072
119
PRD011 Proud Syndrome 42 0.072
120
HMG002 Hemoglobinuria 49 0.072
121
P PSR002 Psoriasis 63 0.072
122
OCL009 Ocular Cancer 61 0.071
123
P HRT032 Heart Disease 64 0.071
124
HRT007 Heart Cancer 51 0.070
125
c SCN042 Secondary Hypereosinophilic Syndrome 15 0.070
126
c CRN214 Coronary Heart Disease 5 22 0.070
127
P PLM037 Pulmonary Hypertension 78 0.070
128
P HRT017 Heart Tumor 34 0.070
129
c ADL079 Adult Heart Tumor 17 0.070
130
c CNG401 Congenital Heart Disease 67 0.069
131
LYM019 Lymphosarcoma 52 0.067
132
PRN039 Paraneoplastic Syndromes 42 0.066
133
NTR018 Neutrophilia, Hereditary 32 0.065
134
P SHR029 Short Syndrome 60 0.065
135
SKN023 Skin Tag 48 0.065
136
c ACT009 Acute Monocytic Leukemia 46 0.065
137
P APL001 Aplastic Anemia 74 0.065
138
P HYP071 Hypersensitivity Reaction Type Ii Disease 46 0.065
139
c MLT019 Multiple Myeloma 77 0.064
140
RPR002 Reproductive System Disease 45 0.064
141
P TCL004 T-Cell Leukemia 44 0.063
142
VND001 Vein Disease 51 0.063
143
WSC001 Wisconsin Syndrome 16 0.063
144
c ATM010 Autoimmune Hemolytic Anemia 59 0.063
145
P PLY041 Polymyositis 49 0.063
146
c LYM106 Lymphoproliferative Syndrome 1 33 0.063
147
WST001 West Syndrome 61 0.063
148
P NRV006 Nervous System Cancer 62 0.062
149
ACT200 Acute Monoblastic Leukemia 44 0.062
150
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.062
151
P MSC005 Muscular Dystrophy 64 0.061
152
GLC077 Glucocorticoid Therapy, Response to 17 0.060
153
HYP266 Hypoxia 55 0.059
154
P NRF002 Neurofibromatosis 66 0.059
155
CRY005 Cryptococcosis 50 0.059
156
P EXN002 Exanthem 57 0.058
157
c LYM107 Lymphoproliferative Syndrome 2 32 0.058
158
FML039 Female Reproductive System Disease 49 0.058
159
PRC012 Pericardial Effusion 50 0.058
160
c NRF018 Neurofibromatosis, Type 1 69 0.058
161
ISC004 Ischemia 56 0.057
162
PRM025 Primary Bacterial Infectious Disease 42 0.056
163
c DLT002 Dilated Cardiomyopathy 75 0.056
164
c CRN173 Coronary Heart Disease 8 19 0.055
165
OLV001 Olivopontocerebellar Atrophy 53 0.055
166
HRT029 Heart Tumor of the Child 16 0.055
167
LVR012 Liver Cirrhosis 71 0.054
168
c CNN010 Connective Tissue Benign Neoplasm 31 0.054
169
c RNL016 Renal Infectious Disease 22 0.053
170
P CRN211 Coronary Artery Disease 74 0.052
171
c TRC078 Trichohepatoenteric Syndrome 2 30 0.052
172
ART111 Artery Disease 56 0.051
173
PRP036 Peripheral T-Cell Lymphoma 44 0.051
174
P HMR012 Hemorrhagic Fever 55 0.051
175
c ADL017 Adult T-Cell Leukemia 59 0.051
176
PRT011 Protein C Deficiency 52 0.050
177
URN008 Urinary Bladder Cancer 64 0.050
178
PYD001 Pyoderma Gangrenosum 48 0.050
179
CNG034 Congestive Heart Failure 72 0.050
180
ACT058 Active Peptic Ulcer Disease 44 0.049
181
ACT177 Acute Basophilic Leukemia 34 0.049
182
PYD002 Pyoderma 46 0.049
183
MVD001 Moved to 60 0.048
184
MLN008 Melanoma 61 0.048
185
c THR092 Thrombophilia Due to Thrombin Defect 56 0.048
186
MNC004 Monoclonal Paraproteinemia 35 0.047
187
P HNT016 Huntington Disease 80 0.046
188
c ESN023 Eosinophilia, Familial 19 0.046
189
MYL003 Myeloid Sarcoma 48 0.045
190
MYL013 Myeloperoxidase Deficiency 46 0.045
191
NVS004 Nova Syndrome 18 0.045
192
INT253 Intestinal Benign Neoplasm 48 0.044
193
DRF001 Dirofilariasis 38 0.043
194
BLD044 Bladder Disease 50 0.043
195
P TRT010 Teratoma 49 0.042
196
WRT001 Worth's Syndrome 37 0.040
197
GLC037 Glucocorticoid Resistance 57 0.039
198
HYP319 Hypereosinophilic Syndrome, Idiopathic, Resistant to Imatinib 39 0.038
199
AGG002 Aggressive Systemic Mastocytosis 42 0.035
200
c DLT001 Delta Chain Disease 14 0.035