Search results for eosinophilic myeloproliferative disorder

206 hits were found for eosinophilic myeloproliferative disorder

# Family MCID Name MIFTS Score
1
MYL015 Myeloproliferative Disorder with Eosinophilia 34 6.026
2
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 17 4.282
3
MYL031 Myeloproliferative Neoplasm 58 0.453
4
P LKM002 Leukemia 71 0.425
5
P ESP024 Esophagitis 61 0.396
6
P AST005 Asthma 82 0.320
7
P HYP098 Hypereosinophilic Syndrome 63 0.273
8
P MNN013 Meningitis 67 0.224
9
ESN006 Eosinophilic Meningitis 33 0.216
10
LKC003 Leukocyte Disease 43 0.215
11
P MYL005 Myelofibrosis 67 0.212
12
P LYM118 Lymphoma 69 0.206
13
THR024 Thrombosis 57 0.205
14
P MYL006 Myeloid Leukemia 66 0.200
15
BNM001 Bone Marrow Cancer 51 0.200
16
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.197
17
MYL009 Myelodysplastic Syndrome 73 0.196
18
THR004 Thrombocytosis 55 0.196
19
DWN001 Down Syndrome 66 0.192
20
MRG013 Mirage Syndrome 29 0.190
21
CHR563 Chronic Eosinophilic Leukemia 46 0.186
22
P PLY018 Polycythemia 58 0.178
23
END072 Endotheliitis 42 0.178
24
WLL006 Wells Syndrome 59 0.175
25
PRM243 Primary Bone Cancer 29 0.168
26
BNS002 Bone Structure Disease 37 0.164
27
MYL004 Myelodysplastic Myeloproliferative Cancer 45 0.161
28
DRM006 Dermatitis 66 0.158
29
BNC003 Bone Cancer 58 0.156
30
c ACT073 Acute Leukemia 60 0.155
31
P HPT021 Hepatitis 69 0.155
32
HMT002 Hematologic Cancer 64 0.151
33
CHR285 Chronic Myelomonocytic Leukemia 56 0.144
34
P ATP001 Atopic Dermatitis 62 0.143
35
PLY125 Polycythemia Vera, Somatic 63 0.139
36
c CHR418 Chronic Leukemia 47 0.133
37
BLD053 Blood Platelet Disease 46 0.132
38
VSC011 Vasculitis 62 0.132
39
P LKM068 Leukemia, Chronic Myeloid, Somatic 68 0.131
40
ALR002 Al-Raqad Syndrome 36 0.127
41
P MST009 Mastocytosis 56 0.126
42
PHY002 Physical Disorder 43 0.126
43
ACD009 Acid-Labile Subunit, Deficiency of 45 0.125
44
c LKM061 Leukemia, Acute Myeloid 73 0.125
45
ALL026 Allergic Hypersensitivity Disease 52 0.123
46
INC022 Inclusion-Cell Disease 46 0.122
47
CRB009 Cerebritis 39 0.121
48
LRN003 Learning Disability 49 0.120
49
c AST039 Asthma 2 28 0.118
50
P LYM026 Lymphoblastic Leukemia 62 0.117
51
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.116
52
P MYS005 Myositis 57 0.115
53
ATN002 Autonomic Nervous System Disease 48 0.115
54
CHL071 Child Syndrome 58 0.115
55
KDS001 Kid Syndrome 53 0.114
56
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 49 0.114
57
CSY001 C Syndrome 50 0.110
58
PLM035 Pulmonary Eosinophilia 46 0.110
59
ALN001 Aland Island Eye Disease 45 0.109
60
ADL002 Adult Syndrome 52 0.107
61
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.106
62
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.106
63
PDG001 Pdgfra-Associated Chronic Eosinophilic Leukemia 12 0.105
64
c SYS004 Systemic Mastocytosis 60 0.105
65
DSS003 Disseminated Eosinophilic Collagen Disease 15 0.104
66
BLD054 Blood Protein Disease 37 0.101
67
LNG099 Lung Disease 64 0.098
68
P HRT032 Heart Disease 75 0.098
69
MTH009 Mouth Disease 61 0.095
70
P LYM033 Lymphoproliferative Syndrome 56 0.095
71
LYM040 Lymphoblastic Lymphoma 53 0.094
72
BRT030 Birth Defects 43 0.092
73
CNN005 Connective Tissue Disease 62 0.092
74
HMT018 Hematopoietic Stem Cell Transplantation 41 0.091
75
PRP019 Peripheral Nervous System Disease 55 0.090
76
WTH001 Withdrawal Disorder 37 0.089
77
P SPS003 Spastic Diplegia 52 0.089
78
c PRM149 Primary Hypereosinophilic Syndrome 38 0.089
79
SRC014 Sarcoma 66 0.089
80
ULC004 Ulcerative Colitis 76 0.088
81
ACR041 Acromelic Frontonasal Dysostosis 45 0.087
82
RFR010 Refractory Anemia 45 0.086
83
PRT036 Peritonitis 63 0.085
84
LYM024 Lymphatic System Disease 52 0.085
85
AND005 Androgen Insensitivity Syndrome, Mild 16 0.084
86
P ENC018 Encephalopathy 59 0.084
87
SPL018 Splenomegaly 44 0.083
88
c ACT020 Acute T Cell Leukemia 35 0.081
89
IMM136 Immune System Disease 51 0.081
90
ADJ001 Adjustment Disorder 38 0.080
91
MYL052 Myeloproliferative Neoplasms, Familial 15 0.080
92
SKN016 Skin Disease 66 0.080
93
c SYS001 Systemic Lupus Erythematosus 86 0.079
94
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.078
95
P THR014 Thrombocytopenia 64 0.078
96
P CRD011 Cardiomyopathy 68 0.077
97
P PSR002 Psoriasis 61 0.075
98
VSC006 Vascular Cancer 51 0.075
99
c LYM107 Lymphoproliferative Syndrome 2 50 0.074
100
CHR286 Chronic Neutrophilic Leukemia 43 0.074
101
PNN001 Panniculitis 51 0.074
102
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 62 0.074
103
P PRT013 Portal Hypertension 60 0.074
104
P HML002 Hemolytic Anemia 62 0.072
105
HMG002 Hemoglobinuria 48 0.072
106
HRT007 Heart Cancer 46 0.071
107
P HRT017 Heart Tumor 32 0.071
108
PRD011 Proud Syndrome 42 0.071
109
PRN039 Paraneoplastic Syndromes 32 0.071
110
c ADL079 Adult Heart Tumor 16 0.070
111
SPC003 Specific Developmental Disorder 38 0.070
112
c CHR417 Chronic Graft Versus Host Disease 51 0.070
113
P PLM036 Pulmonary Fibrosis 71 0.069
114
ISC004 Ischemia 61 0.069
115
OCL009 Ocular Cancer 59 0.068
116
MST017 Mast Cell Disease 50 0.068
117
P BRS047 Breast Cancer 100 0.068
118
PRP030 Purpura 58 0.067
119
CRD118 Cardiovascular Cancer 44 0.067
120
TBR010 Tuberculosis 70 0.067
121
VND001 Vein Disease 47 0.067
122
P LVR013 Liver Disease 75 0.066
123
WST001 West Syndrome 57 0.066
124
P SHR029 Short Syndrome 58 0.066
125
c SCN042 Secondary Hypereosinophilic Syndrome 14 0.066
126
c LYM106 Lymphoproliferative Syndrome 1 32 0.065
127
P PLY041 Polymyositis 52 0.064
128
HDG012 Hodgkin Lymphoma 77 0.064
129
NTR005 Nutritional Deficiency Disease 36 0.064
130
HYP266 Hypoxia 56 0.064
131
UPP004 Upper Respiratory Tract Disease 46 0.064
132
WSC001 Wisconsin Syndrome 14 0.063
133
P ACT135 Acute Graft Versus Host Disease 53 0.062
134
P TCL004 T-Cell Leukemia 47 0.062
135
DRG003 Drug Dependence 50 0.062
136
P APL001 Aplastic Anemia 75 0.062
137
GLC077 Glucocorticoid Therapy, Response to 16 0.061
138
P NRV006 Nervous System Cancer 60 0.060
139
P MLT019 Multiple Myeloma 83 0.059
140
ACT200 Acute Monoblastic Leukemia 42 0.059
141
c ATM010 Autoimmune Hemolytic Anemia 60 0.059
142
ART111 Artery Disease 55 0.058
143
c CRN214 Coronary Heart Disease 5 22 0.058
144
P CRN211 Coronary Artery Disease 74 0.058
145
HRT029 Heart Tumor of the Child 15 0.058
146
HPT074 Hepatic Adenoma, Somatic 50 0.057
147
NTR018 Neutrophilia, Hereditary 42 0.057
148
MLN008 Melanoma 62 0.056
149
PRC012 Pericardial Effusion 51 0.056
150
c RNL016 Renal Infectious Disease 20 0.056
151
c TRC078 Trichohepatoenteric Syndrome 2 29 0.055
152
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.055
153
ESN023 Eosinophilia, Familial 17 0.055
154
c CRN173 Coronary Heart Disease 8 18 0.055
155
SKN023 Skin Tag 44 0.054
156
LYM019 Lymphosarcoma 53 0.054
157
PRP027 Peripheral Vascular Disease 68 0.054
158
P NRF002 Neurofibromatosis 71 0.053
159
MYL013 Myeloperoxidase Deficiency 46 0.052
160
c NRF018 Neurofibromatosis, Type 1 67 0.051
161
c CNN010 Connective Tissue Benign Neoplasm 32 0.051
162
SPN369 Spinal Disease 39 0.050
163
P HNT016 Huntington Disease 80 0.050
164
ANG054 Angina Pectoris 50 0.050
165
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.049
166
MYL003 Myeloid Sarcoma 48 0.049
167
c ADL017 Adult T-Cell Leukemia 60 0.049
168
ATM012 Autoimmune Disease of Blood 35 0.049
169
PRP036 Peripheral T-Cell Lymphoma 45 0.048
170
P PNC001 Pancytopenia 52 0.048
171
c BNG076 Benign Exophthalmos Syndrome 15 0.048
172
ACT177 Acute Basophilic Leukemia 34 0.048
173
PLM033 Pulmonary Embolism 60 0.048
174
P HYP086 Hypothyroidism 64 0.048
175
PRT011 Protein C Deficiency 52 0.047
176
c THR092 Thrombophilia Due to Thrombin Defect 54 0.047
177
CNG034 Congestive Heart Failure 72 0.047
178
PYD001 Pyoderma Gangrenosum 51 0.047
179
PYD002 Pyoderma 48 0.047
180
P HML001 Hemolytic-Uremic Syndrome 51 0.046
181
THR035 Thrombasthenia 39 0.046
182
OLV001 Olivopontocerebellar Atrophy 53 0.046
183
NVS004 Nova Syndrome 13 0.045
184
LVR012 Liver Cirrhosis 67 0.045
185
WLL001 Williams-Beuren Syndrome 60 0.044
186
GLC037 Glucocorticoid Resistance 62 0.043
187
ENG004 Engraftment Syndrome 32 0.043
188
BLD044 Bladder Disease 51 0.042
189
PRM025 Primary Bacterial Infectious Disease 41 0.042
190
c DLT002 Dilated Cardiomyopathy 76 0.040
191
P EXN002 Exanthem 57 0.040
192
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.040
193
c HPT003 Hepatitis a 59 0.039
194
c PSR017 Psoriasis 2 37 0.039
195
PSR005 Psoriasis, Protection Against 32 0.039
196
c PSR019 Psoriasis Susceptibility 13 32 0.039
197
DRF001 Dirofilariasis 37 0.038
198
WRT001 Worth's Syndrome 34 0.038
199
MNC004 Monoclonal Paraproteinemia 34 0.037
200
c DLT001 Delta Chain Disease 13 0.037
201
THR016 Thrombophlebitis 53 0.035
202
P AFB001 Afibrinogenemia 48 0.035
203
CRY005 Cryptococcosis 50 0.035
204
CTN014 Cutaneous Mastocytosis 49 0.034
205
HYP319 Hypereosinophilic Syndrome, Idiopathic, Resistant to Imatinib 39 0.034
206
URN008 Urinary Bladder Cancer 66 0.033
Content
Loading form....