Search results for eosinophilic myeloproliferative disorder

171 hits were found for eosinophilic myeloproliferative disorder

# Family MCID Name MIFTS Score
1
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 27 6.018
2
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 29 4.397
3
MYL031 Myeloproliferative Neoplasm 64 0.577
4
P LKM002 Leukemia 75 0.489
5
P ESP024 Esophagitis 64 0.405
6
AST005 Asthma 83 0.338
7
P MYL005 Myelofibrosis 75 0.267
8
P HYP098 Hypereosinophilic Syndrome 65 0.250
9
P LYM118 Lymphoma 71 0.246
10
THR024 Thrombosis 61 0.244
11
P MYL006 Myeloid Leukemia 69 0.241
12
MYL009 Myelodysplastic Syndrome 75 0.239
13
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.238
14
THR004 Thrombocytosis 55 0.237
15
P MNN013 Meningitis 71 0.227
16
DWN001 Down Syndrome 70 0.227
17
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.223
18
PLY001 Polycythemia Vera 75 0.222
19
ESN006 Eosinophilic Meningitis 38 0.221
20
P PLY018 Polycythemia 60 0.217
21
LKC003 Leukocyte Disease 34 0.213
22
CHR563 Chronic Eosinophilic Leukemia 51 0.201
23
P ESS003 Essential Thrombocythemia 71 0.194
24
c LKM061 Leukemia, Acute Myeloid 81 0.192
25
END072 Endotheliitis 46 0.192
26
P CHR285 Chronic Myelomonocytic Leukemia 63 0.188
27
c LKM063 Leukemia, Chronic Myeloid 80 0.174
28
P HPT021 Hepatitis 75 0.170
29
HYP810 Hypereosinophilic Syndrome, Idiopathic 57 0.170
30
DRM006 Dermatitis 67 0.166
31
LNG099 Lung Disease 67 0.154
32
AGN016 Aging 65 0.153
33
P DRM053 Dermatitis, Atopic 68 0.152
34
c JVN004 Juvenile Myelomonocytic Leukemia 70 0.148
35
BNM001 Bone Marrow Cancer 52 0.147
36
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.147
37
HMT002 Hematologic Cancer 64 0.145
38
CRB009 Cerebritis 41 0.144
39
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.141
40
VSC011 Vasculitis 66 0.140
41
P ANR048 Aniridia 1 68 0.138
42
ANR038 Anorexia Nervosa 1 21 0.138
43
BLD137 Blood Group--Ahonen 17 0.137
44
P LYM026 Lymphoblastic Leukemia 66 0.137
45
c ACT073 Acute Leukemia 61 0.137
46
c BLD140 Blood Group, I System 37 0.136
47
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 53 0.134
48
SYS004 Systemic Mastocytosis 65 0.134
49
ATY042 Atypical Chronic Myeloid Leukemia 51 0.129
50
P MYS005 Myositis 63 0.122
51
ALR002 Al-Raqad Syndrome 30 0.118
52
P ART022 Arthritis 77 0.117
53
RFR010 Refractory Anemia 48 0.113
54
BDD001 Budd-Chiari Syndrome 58 0.113
55
DSS003 Disseminated Eosinophilic Collagen Disease 20 0.112
56
P GRF003 Graft-Versus-Host Disease 72 0.108
57
LYM040 Lymphoblastic Lymphoma 58 0.108
58
SPS003 Spastic Diplegia 55 0.107
59
SRC014 Sarcoma 68 0.105
60
HMT018 Hematopoietic Stem Cell Transplantation 58 0.104
61
P KDN018 Kidney Disease 69 0.103
62
ALL026 Allergic Hypersensitivity Disease 59 0.103
63
SPL018 Splenomegaly 45 0.102
64
PLY150 Polykaryocytosis Inducer 20 0.101
65
LYM024 Lymphatic System Disease 45 0.099
66
c PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 25 0.095
67
ACT119 Acute Promyelocytic Leukemia 64 0.094
68
P MLT020 Multiple Sclerosis 85 0.091
69
LYM067 Lymphoid Leukemia 43 0.090
70
CHR286 Chronic Neutrophilic Leukemia 49 0.090
71
P THR014 Thrombocytopenia 65 0.089
72
P ENC018 Encephalopathy 58 0.089
73
P LVR013 Liver Disease 76 0.089
74
ATM095 Autoimmune Disease 66 0.088
75
c LKM062 Leukemia, Acute Lymphoblastic 64 0.088
76
ULC004 Ulcerative Colitis 80 0.087
77
HMG002 Hemoglobinuria 52 0.087
78
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.087
79
PRT036 Peritonitis 67 0.085
80
P ACT074 Acute Lymphocytic Leukemia 61 0.084
81
c LKM071 Leukemia, Chronic Lymphocytic 75 0.084
82
BLD163 Blood Group, Dombrock System 23 0.084
83
P PRT013 Portal Hypertension 59 0.083
84
c LKM004 Leukemia, B-Cell, Chronic 37 0.083
85
MST017 Mast Cell Disease 63 0.082
86
P DBT009 Diabetes Mellitus 72 0.082
87
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.082
88
P PSR002 Psoriasis 65 0.081
89
PRN039 Paraneoplastic Syndromes 35 0.078
90
ACT200 Acute Monoblastic Leukemia 47 0.077
91
ACT113 Acute Myeloblastic Leukemia with Maturation 40 0.077
92
PNN001 Panniculitis 48 0.077
93
LYM019 Lymphosarcoma 58 0.077
94
P HRT032 Heart Disease 80 0.077
95
P BRS047 Breast Cancer 100 0.076
96
NTR018 Neutrophilia, Hereditary 46 0.075
97
P RNG031 Ring Chromosome Y Syndrome 29 0.074
98
P MNC007 Monocytic Leukemia 59 0.073
99
HYP266 Hypoxia 61 0.072
100
HPT082 Hepatic Adenomas, Familial 52 0.072
101
MYL003 Myeloid Sarcoma 51 0.071
102
MYL069 Myeloma, Multiple 86 0.070
103
NRF026 Neurofibromatosis, Type Iv, of Riccardi 72 0.070
104
LYM133 Lymphoma, Hodgkin, Classic 78 0.069
105
P RFR008 Refractory Anemia with Excess Blasts 34 0.069
106
P PLY041 Polymyositis 57 0.068
107
c LKM056 Leukemia, Chronic Lymphocytic 2 35 0.068
108
P HRD009 Hereditary Wilms' Tumor 46 0.068
109
MLN008 Melanoma 72 0.067
110
c LKM070 Leukemia, Acute Monocytic 55 0.067
111
MYL013 Myeloperoxidase Deficiency 42 0.067
112
P TCL004 T-Cell Leukemia 50 0.067
113
PST011 Pustulosis of Palm and Sole 47 0.066
114
P MYC084 Mycobacterium Tuberculosis 1 69 0.065
115
P HML002 Hemolytic Anemia 62 0.064
116
ART140 Arteries, Anomalies of 51 0.064
117
ISC004 Ischemia 66 0.063
118
P HYP086 Hypothyroidism 62 0.063
119
P PLM036 Pulmonary Fibrosis 68 0.062
120
VSC007 Vascular Disease 71 0.062
121
c PRM149 Primary Hypereosinophilic Syndrome 35 0.062
122
LYM052 Lymphomatoid Papulosis 45 0.061
123
P TMP003 Temporal Arteritis 67 0.061
124
P PRC012 Pericardial Effusion 52 0.060
125
c TRC078 Trichohepatoenteric Syndrome 2 34 0.060
126
ACT177 Acute Basophilic Leukemia 37 0.060
127
PYD001 Pyoderma Gangrenosum 55 0.059
128
PYD002 Pyoderma 51 0.058
129
P NTR004 Neutropenia 60 0.058
130
P ANT006 Antiphospholipid Syndrome 59 0.057
131
HMP001 Hemopericardium 34 0.057
132
c ANM038 Anemia, Autoimmune Hemolytic 56 0.055
133
LYM143 Lymphoma, Non-Hodgkin, Familial 71 0.055
134
MLL018 Miller-Dieker Lissencephaly Syndrome 47 0.055
135
EWN003 Ewing Sarcoma 72 0.054
136
c LKM060 Leukemia, Acute Lymphoblastic 3 49 0.052
137
ACT103 Acute Lymphoblastic Leukemia, Childhood 53 0.052
138
CNG034 Congestive Heart Failure 74 0.052
139
c SVR003 Severe Congenital Neutropenia 58 0.051
140
c PSR018 Psoriasis 13 39 0.049
141
c WLM011 Wilms Tumor 6 44 0.049
142
HRT015 Heritable Pulmonary Arterial Hypertension 48 0.048
143
DSS009 Disseminated Intravascular Coagulation 56 0.048
144
GST019 Gastrointestinal Stromal Tumor 74 0.047
145
DSM004 Desmoid Tumor 63 0.047
146
CHR178 Chromosomal Triplication 35 0.047
147
PNC001 Pancytopenia 50 0.046
148
P DLT002 Dilated Cardiomyopathy 76 0.046
149
PPL059 Popliteal Pterygium Syndrome, Lethal Type 37 0.045
150
c ACT135 Acute Graft Versus Host Disease 57 0.045
151
CRN273 Corneal Dystrophy, Subepithelial Mucinous 32 0.045
152
IMM158 Immune Suppression 57 0.045
153
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 51 0.045
154
ESP002 Esophageal Varix 46 0.044
155
P EXN002 Exanthem 62 0.044
156
BNF002 Bone Fracture 56 0.043
157
CTN014 Cutaneous Mastocytosis 50 0.043
158
c WLM018 Wilms Tumor 5 49 0.043
159
ATM052 Autoimmune Disease 1 30 0.043
160
LVR012 Liver Cirrhosis 73 0.042
161
LRG008 Large Granular Lymphocyte Leukemia 49 0.042
162
P PLM006 Pulmonary Alveolar Proteinosis 49 0.040
163
P LPR002 Leopard Syndrome 56 0.040
164
PRT011 Protein C Deficiency 48 0.039
165
CRY005 Cryptococcosis 54 0.038
166
MST002 Mast-Cell Leukemia 51 0.037
167
PLM068 Pulmonary Vein Stenosis 43 0.037
168
VSC006 Vascular Cancer 43 0.037
169
MN1001 Mn1 32 0.037
170
ACT234 Acute Myeloid Leukemia with Minimal Differentiation 24 0.037
171
TTR021 Tetrasomy 21 21 0.037
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