Search results for eosinophilic myeloproliferative disorder

185 hits were found for eosinophilic myeloproliferative disorder

# Family MCID Name MIFTS Score
1
MYL015 Myeloproliferative Disorder with Eosinophilia 35 5.937
2
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 16 4.228
3
MYL031 Myeloproliferative Neoplasm 57 0.481
4
P LKM002 Leukemia 72 0.442
5
P ESP024 Esophagitis 59 0.404
6
P AST005 Asthma 81 0.335
7
P HYP098 Hypereosinophilic Syndrome 61 0.229
8
P MNN013 Meningitis 65 0.227
9
ESN006 Eosinophilic Meningitis 33 0.220
10
P LYM118 Lymphoma 69 0.218
11
THR024 Thrombosis 43 0.212
12
P MYL006 Myeloid Leukemia 64 0.205
13
THR004 Thrombocytosis 52 0.203
14
MYL009 Myelodysplastic Syndrome 71 0.202
15
BNS002 Bone Structure Disease 36 0.202
16
DWN001 Down Syndrome 69 0.197
17
P PLY018 Polycythemia 56 0.188
18
CHR563 Chronic Eosinophilic Leukemia 46 0.188
19
BNM001 Bone Marrow Cancer 51 0.187
20
END072 Endotheliitis 41 0.180
21
LKC003 Leukocyte Disease 46 0.179
22
WLL006 Wells Syndrome 58 0.176
23
MTH009 Mouth Disease 62 0.165
24
DRM006 Dermatitis 63 0.161
25
P HYP729 Hypersensitivity Reaction Disease 43 0.158
26
P HPT021 Hepatitis 68 0.157
27
NLL002 Null Syndrome 26 0.156
28
P CHR285 Chronic Myelomonocytic Leukemia 58 0.156
29
LNG099 Lung Disease 61 0.151
30
ADL002 Adult Syndrome 57 0.150
31
P ATP001 Atopic Dermatitis 60 0.145
32
PHY002 Physical Disorder 43 0.144
33
HMT002 Hematologic Cancer 62 0.143
34
c PRM012 Primary Polycythemia 53 0.139
35
c ACT073 Acute Leukemia 61 0.137
36
VSC011 Vasculitis 62 0.135
37
c CHR418 Chronic Leukemia 43 0.132
38
BLD053 Blood Platelet Disease 46 0.130
39
BRT030 Birth Defects 44 0.128
40
IMM136 Immune System Disease 53 0.127
41
CRB009 Cerebritis 39 0.127
42
PRP019 Peripheral Nervous System Disease 53 0.121
43
P LYM026 Lymphoblastic Leukemia 60 0.118
44
P MYS005 Myositis 56 0.118
45
c LKM061 Leukemia, Acute Myeloid 74 0.118
46
CHL071 Child Syndrome 59 0.117
47
KDS001 Kid Syndrome 57 0.116
48
P ART022 Arthritis 72 0.113
49
ATN002 Autonomic Nervous System Disease 48 0.109
50
BLD054 Blood Protein Disease 39 0.109
51
SYS004 Systemic Mastocytosis 60 0.109
52
PDG001 Pdgfra-Associated Chronic Eosinophilic Leukemia 15 0.107
53
ALR002 Al-Raqad Syndrome 29 0.107
54
DSS003 Disseminated Eosinophilic Collagen Disease 17 0.105
55
c AST039 Asthma 2 31 0.104
56
c MYL058 Myeloproliferative Syndrome, Transient 34 0.104
57
CSY001 C Syndrome 53 0.103
58
P SPS003 Spastic Diplegia 52 0.098
59
P KDN018 Kidney Disease 65 0.094
60
SRC014 Sarcoma 66 0.092
61
HMT018 Hematopoietic Stem Cell Transplantation 40 0.092
62
LYM024 Lymphatic System Disease 49 0.092
63
AND005 Androgen Insensitivity Syndrome, Mild 16 0.091
64
RFR010 Refractory Anemia 45 0.088
65
LYM040 Lymphoblastic Lymphoma 52 0.086
66
SPL018 Splenomegaly 45 0.085
67
ULC004 Ulcerative Colitis 72 0.085
68
MYL052 Myeloproliferative Neoplasms, Familial 19 0.084
69
PRT036 Peritonitis 60 0.084
70
P MYP004 Myopathy 68 0.082
71
ADJ001 Adjustment Disorder 38 0.082
72
P CRD011 Cardiomyopathy 67 0.079
73
P THR014 Thrombocytopenia 63 0.079
74
c PRM149 Primary Hypereosinophilic Syndrome 39 0.079
75
P PRT013 Portal Hypertension 58 0.078
76
ART111 Artery Disease 55 0.078
77
P MSC033 Muscle Disorders 52 0.078
78
c CHR090 Chronic Lymphocytic Leukemia 75 0.078
79
P LVR013 Liver Disease 72 0.077
80
WTH001 Withdrawal Disorder 40 0.076
81
P PSR002 Psoriasis 64 0.076
82
PNN001 Panniculitis 49 0.075
83
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 62 0.074
84
HMG002 Hemoglobinuria 48 0.074
85
P HRT032 Heart Disease 75 0.074
86
LYM019 Lymphosarcoma 53 0.072
87
RPR002 Reproductive System Disease 43 0.072
88
PRN039 Paraneoplastic Syndromes 31 0.071
89
c CHR417 Chronic Graft Versus Host Disease 50 0.070
90
P BRS047 Breast Cancer 100 0.070
91
HYP319 Hypereosinophilic Syndrome, Idiopathic, Resistant to Imatinib 43 0.069
92
SKN023 Skin Tag 46 0.069
93
HYP266 Hypoxia 55 0.069
94
TBR010 Tuberculosis 69 0.069
95
P PLM036 Pulmonary Fibrosis 68 0.069
96
VND001 Vein Disease 49 0.068
97
PRP030 Purpura 57 0.068
98
P LYM033 Lymphoproliferative Syndrome 54 0.068
99
P PLY041 Polymyositis 52 0.067
100
HDG012 Hodgkin Lymphoma 73 0.066
101
MST017 Mast Cell Disease 61 0.066
102
HRT007 Heart Cancer 46 0.065
103
P LKM068 Leukemia, Chronic Myeloid, Somatic 64 0.065
104
P ENC018 Encephalopathy 52 0.064
105
SXL003 Sexual Disorder 42 0.064
106
P HRT017 Heart Tumor 34 0.064
107
c TRC078 Trichohepatoenteric Syndrome 2 34 0.064
108
P HML002 Hemolytic Anemia 61 0.062
109
P ACT135 Acute Graft Versus Host Disease 52 0.062
110
ISC004 Ischemia 59 0.061
111
ACT200 Acute Monoblastic Leukemia 42 0.061
112
c LYM106 Lymphoproliferative Syndrome 1 36 0.061
113
P LNG032 Lung Cancer 94 0.060
114
P MLT019 Multiple Myeloma 82 0.060
115
c ATM010 Autoimmune Hemolytic Anemia 60 0.059
116
GLC077 Glucocorticoid Therapy, Response to 18 0.059
117
PRC012 Pericardial Effusion 50 0.058
118
c SCN042 Secondary Hypereosinophilic Syndrome 16 0.058
119
MLN008 Melanoma 70 0.058
120
CNT098 Central Core Disease 66 0.058
121
LYM052 Lymphomatoid Papulosis 40 0.058
122
HPT074 Hepatic Adenoma, Somatic 44 0.058
123
c AST051 Asthma Susceptibility, Phf11-Related 20 0.058
124
MYL013 Myeloperoxidase Deficiency 46 0.057
125
P MSC005 Muscular Dystrophy 65 0.056
126
P TCL004 T-Cell Leukemia 46 0.055
127
VSC007 Vascular Disease 65 0.055
128
P NRF018 Neurofibromatosis, Type 1 78 0.055
129
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.054
130
PYD001 Pyoderma Gangrenosum 50 0.054
131
c LYM107 Lymphoproliferative Syndrome 2 53 0.053
132
PYD002 Pyoderma 47 0.053
133
CNG034 Congestive Heart Failure 70 0.052
134
PLM033 Pulmonary Embolism 59 0.052
135
UPP004 Upper Respiratory Tract Disease 46 0.052
136
ACT177 Acute Basophilic Leukemia 33 0.049
137
ANG054 Angina Pectoris 49 0.049
138
MYL003 Myeloid Sarcoma 47 0.049
139
NRL004 Neuroleptic Malignant Syndrome 40 0.048
140
ATM012 Autoimmune Disease of Blood 37 0.048
141
THR035 Thrombasthenia 41 0.048
142
LVR012 Liver Cirrhosis 66 0.046
143
MLG056 Malignant Hyperthermia 57 0.045
144
GLC037 Glucocorticoid Resistance 59 0.044
145
P HML001 Hemolytic-Uremic Syndrome 49 0.044
146
BLD044 Bladder Disease 50 0.043
147
DCH001 Duchenne Muscular Dystrophy 79 0.043
148
c DLT002 Dilated Cardiomyopathy 74 0.042
149
P EXN002 Exanthem 57 0.042
150
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 29 0.041
151
c ACT075 Acute Myocardial Infarction 59 0.041
152
c CNG464 Congenital Myopathy 50 0.041
153
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 43 0.041
154
ASP004 Asphyxia Neonatorum 38 0.040
155
DRF001 Dirofilariasis 38 0.040
156
c PSR019 Psoriasis Susceptibility 13 29 0.040
157
PSR005 Psoriasis, Protection Against 24 0.040
158
MYT003 Myotonic Disease 32 0.040
159
c HPT003 Hepatitis a 56 0.040
160
MSC051 Muscular Dystrophy, Rigid Spine, 1 45 0.039
161
c RNL016 Renal Infectious Disease 23 0.039
162
MNC004 Monoclonal Paraproteinemia 36 0.038
163
CRD119 Cardiac Arrest 59 0.038
164
c HRD009 Hereditary Wilms' Tumor 40 0.038
165
c THR092 Thrombophilia Due to Thrombin Defect 50 0.038
166
P RPP002 Rippling Muscle Disease 42 0.038
167
DST004 Distal Muscular Dystrophy 38 0.038
168
THR016 Thrombophlebitis 52 0.037
169
P CNG046 Congenital Fiber-Type Disproportion 49 0.037
170
PRX075 Proximal Myopathy and Ophthalmoplegia 33 0.037
171
P CNT004 Centronuclear Myopathy 52 0.037
172
INT007 Intermediate Coronary Syndrome 50 0.037
173
PRT011 Protein C Deficiency 49 0.037
174
URN008 Urinary Bladder Cancer 63 0.036
175
c VNT013 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1 53 0.036
176
c MSC124 Muscular Dystrophy, Congenital 54 0.036
177
ORB010 Orbital Granuloma 25 0.036
178
P ULL002 Ullrich Congenital Muscular Dystrophy 1 46 0.035
179
ISC002 Ischemic Optic Neuropathy 44 0.035
180
CLD011 Cold Urticaria 30 0.035
181
CRY005 Cryptococcosis 50 0.035
182
P BTH005 Bethlem Myopathy 1 46 0.035
183
FML036 Familial Periodic Paralysis 41 0.035
184
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 52 0.034
185
CTN014 Cutaneous Mastocytosis 47 0.034
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