Search results for jak2

187 hits were found for jak2

# Family MCID Name MIFTS Score
1
P MYL005 Myelofibrosis 75 5.754
2
PLY001 Polycythemia Vera 75 5.666
3
BDD001 Budd-Chiari Syndrome 58 4.908
4
P PLY018 Polycythemia 60 4.454
5
c THR086 Thrombocythemia 3 18 4.305
6
P LKM002 Leukemia 75 4.236
7
MYL031 Myeloproliferative Neoplasm 64 4.211
8
P ESS003 Essential Thrombocythemia 71 4.064
9
THR004 Thrombocytosis 55 3.702
10
c LKM061 Leukemia, Acute Myeloid 81 3.577
11
THR024 Thrombosis 61 3.545
12
c ACT073 Acute Leukemia 61 3.403
13
P ERY058 Erythrocytosis, Familial, 1 55 3.403
14
c LKM063 Leukemia, Chronic Myeloid 80 3.117
15
SPL018 Splenomegaly 45 3.060
16
BNM001 Bone Marrow Cancer 52 3.044
17
P THR015 Thrombophilia 58 3.026
18
c SVR003 Severe Congenital Neutropenia 58 3.008
19
ATY042 Atypical Chronic Myeloid Leukemia 51 3.008
20
SYS004 Systemic Mastocytosis 65 2.988
21
P PRT013 Portal Hypertension 59 2.965
22
RFR010 Refractory Anemia 48 2.817
23
MYL009 Myelodysplastic Syndrome 75 2.732
24
P LYM026 Lymphoblastic Leukemia 66 2.732
25
PRT018 Portal Vein Thrombosis 50 2.688
26
P CHR285 Chronic Myelomonocytic Leukemia 63 2.616
27
c PRM012 Primary Polycythemia 53 2.616
28
MGK001 Megakaryocytic Leukemia 63 2.593
29
P INF037 Inflammatory Bowel Disease 52 2.593
30
HMT002 Hematologic Cancer 64 2.568
31
ACT098 Acute Erythroid Leukemia 52 2.568
32
c ACQ010 Acquired Polycythemia 33 2.568
33
MYL004 Myelodysplastic Myeloproliferative Cancer 45 2.175
34
PRM163 Primary Mediastinal Large B-Cell Lymphoma 42 2.175
35
c JVN004 Juvenile Myelomonocytic Leukemia 70 2.152
36
BDY004 Body Mass Index Quantitative Trait Locus 11 75 2.127
37
CRB138 Core Binding Factor Acute Myeloid Leukemia 46 2.127
38
EPS023 Epstein-Barr Virus-Associated Gastric Carcinoma 42 2.127
39
THR009 Thrombocytopenia-Absent Radius Syndrome 58 2.097
40
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 46 2.097
41
ISL114 Isolated Growth Hormone Deficiency, Type Ii 46 2.097
42
c MYS078 Myasthenic Syndrome, Congenital, 14 40 2.097
43
ACQ017 Acquired Von Willebrand Syndrome 40 2.097
44
ISC015 Ischemic Colitis 39 2.097
45
HPT020 Hepatic Vascular Disease 36 2.097
46
MDS019 Mediastinal Malignant Lymphoma 36 2.097
47
LCT003 Lactocele 32 2.097
48
MDS006 Mediastinal Gray Zone Lymphoma 32 2.097
49
MYL002 Myelophthisic Anemia 32 2.097
50
MYL059 Myeloid and Lymphoid Neoplasms with Eosinophilia and Abnormalities of Pdgfra, Pdgfrb, and Fgfr1 31 2.097
51
RGL001 Regular Astigmatism 27 2.097
52
P DMN001 Diamond-Blackfan Anemia 70 1.522
53
BHC003 Behcet Syndrome 68 1.522
54
P BLD051 Blood Coagulation Disease 38 1.522
55
IMM136 Immune System Disease 57 1.483
56
BLD053 Blood Platelet Disease 45 1.483
57
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.372
58
P MYL006 Myeloid Leukemia 69 0.222
59
P LYM118 Lymphoma 71 0.206
60
c THR092 Thrombophilia Due to Thrombin Defect 61 0.189
61
c BLD140 Blood Group, I System 37 0.189
62
c PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 25 0.189
63
P BRS047 Breast Cancer 100 0.134
64
END072 Endotheliitis 46 0.134
65
LYM138 Lymphoblastic Leukemia, Acute, with Lymphomatous Features 24 0.134
66
P BCL006 B-Cell Lymphomas 70 0.125
67
MDS022 Mediastinitis 44 0.125
68
GST053 Gastric Cancer 84 0.116
69
c LKM071 Leukemia, Chronic Lymphocytic 75 0.116
70
DWN001 Down Syndrome 70 0.116
71
c LKM004 Leukemia, B-Cell, Chronic 37 0.116
72
c LKM056 Leukemia, Chronic Lymphocytic 2 35 0.116
73
MYL069 Myeloma, Multiple 86 0.106
74
LYM133 Lymphoma, Hodgkin, Classic 78 0.106
75
AGN016 Aging 65 0.106
76
CHR286 Chronic Neutrophilic Leukemia 49 0.106
77
CRB009 Cerebritis 41 0.106
78
P PNC044 Pancreatitis 64 0.095
79
HMT018 Hematopoietic Stem Cell Transplantation 58 0.095
80
P PNC035 Pancreatic Cancer 89 0.082
81
P MYC007 Myocardial Infarction 81 0.082
82
CRH001 Crohn's Disease 80 0.082
83
ULC004 Ulcerative Colitis 80 0.082
84
P ADN016 Adenocarcinoma 71 0.082
85
P THR014 Thrombocytopenia 65 0.082
86
CLT003 Colitis 63 0.082
87
P NTR004 Neutropenia 60 0.082
88
ALL026 Allergic Hypersensitivity Disease 59 0.082
89
RTN023 Retinitis 52 0.082
90
NTR018 Neutrophilia, Hereditary 46 0.082
91
P PRS040 Prostate Cancer 88 0.067
92
c PLM164 Pulmonary Hypertension, Primary, 1 67 0.067
93
P THL005 Thalassemia 65 0.067
94
c ADL017 Adult T-Cell Leukemia 63 0.067
95
P GLM045 Glioma 61 0.067
96
PRS047 Prostatitis 59 0.067
97
P TCL004 T-Cell Leukemia 50 0.067
98
c ERY048 Erythrocytosis, Familial, 2 48 0.067
99
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.067
100
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 29 0.067
101
P MLT020 Multiple Sclerosis 85 0.047
102
AST005 Asthma 83 0.047
103
P OVR042 Ovarian Cancer 82 0.047
104
P PLM037 Pulmonary Hypertension 79 0.047
105
P HPT021 Hepatitis 75 0.047
106
SQM006 Squamous Cell Carcinoma 74 0.047
107
P FML018 Familial Mediterranean Fever 73 0.047
108
PLM134 Pulmonary Fibrosis, Idiopathic 73 0.047
109
P GRF003 Graft-Versus-Host Disease 72 0.047
110
NRF026 Neurofibromatosis, Type Iv, of Riccardi 72 0.047
111
P NSP012 Nasopharyngeal Carcinoma 71 0.047
112
c SPN225 Spondyloarthropathy 1 71 0.047
113
BRC012 Brucellosis 71 0.047
114
P PNM007 Pneumonia 70 0.047
115
c HMP029 Hemophilia a 69 0.047
116
P PLM036 Pulmonary Fibrosis 68 0.047
117
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.047
118
SRC014 Sarcoma 68 0.047
119
LNG099 Lung Disease 67 0.047
120
ISC004 Ischemia 66 0.047
121
P PSR002 Psoriasis 65 0.047
122
P HYP098 Hypereosinophilic Syndrome 65 0.047
123
DFF005 Diffuse Large B-Cell Lymphoma 64 0.047
124
HYP066 Hyperglycemia 64 0.047
125
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.047
126
c ACT075 Acute Myocardial Infarction 64 0.047
127
P ESP024 Esophagitis 64 0.047
128
ACT119 Acute Promyelocytic Leukemia 64 0.047
129
P SRC025 Sarcoidosis 1 63 0.047
130
LNG108 Langerhans Cell Histiocytosis 63 0.047
131
c NRF024 Neurofibromatosis, Type I 63 0.047
132
P HMP007 Hemophilia 61 0.047
133
P HMR003 Hemorrhagic Disease 61 0.047
134
P FBR017 Fibrosarcoma 61 0.047
135
P HST010 Histiocytosis 60 0.047
136
P INF032 Infertility 59 0.047
137
LYM040 Lymphoblastic Lymphoma 58 0.047
138
GLC003 Glucose Intolerance 58 0.047
139
c ACT135 Acute Graft Versus Host Disease 57 0.047
140
EXT034 Extrinsic Allergic Alveolitis 57 0.047
141
SPN051 Spondylitis 55 0.047
142
P HRD011 Hereditary Spherocytosis 55 0.047
143
PYD001 Pyoderma Gangrenosum 55 0.047
144
P PNM006 Pneumoconiosis 55 0.047
145
c OVR114 Ovarian Cancer 1 54 0.047
146
PRP080 Peripheral Artery Disease 54 0.047
147
P RTN022 Retinal Vein Occlusion 53 0.047
148
HMG002 Hemoglobinuria 52 0.047
149
PYD002 Pyoderma 51 0.047
150
ART140 Arteries, Anomalies of 51 0.047
151
c ACQ014 Acquired Hemophilia 51 0.047
152
PLS009 Plasma Cell Neoplasm 51 0.047
153
CHR563 Chronic Eosinophilic Leukemia 51 0.047
154
VCC001 Vaccinia 50 0.047
155
LYM012 Lymphoplasmacytic Lymphoma 50 0.047
156
c CNT016 Central Retinal Vein Occlusion 50 0.047
157
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.047
158
CHR074 Choriocarcinoma 49 0.047
159
CHR635 Chromosome 5q Deletion Syndrome 49 0.047
160
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.047
161
PST011 Pustulosis of Palm and Sole 47 0.047
162
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.047
163
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.047
164
NSP002 Nasopharyngitis 46 0.047
165
DDN006 Duodenitis 46 0.047
166
P HRD009 Hereditary Wilms' Tumor 46 0.047
167
P RTN014 Retinal Artery Occlusion 45 0.047
168
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.047
169
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.047
170
c ACQ042 Acquired Hemophilia a 44 0.047
171
P BRY005 Beryllium Disease 43 0.047
172
c CHR576 Chronic Beryllium Disease 42 0.047
173
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.047
174
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.047
175
BRY001 Berylliosis 42 0.047
176
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 41 0.047
177
c CNT028 Central Retinal Artery Occlusion 40 0.047
178
ANT018 Anthracosis 39 0.047
179
PPL059 Popliteal Pterygium Syndrome, Lethal Type 37 0.047
180
VSC008 Vascular Hemostatic Disease 36 0.047
181
PLC006 Placental Choriocarcinoma 35 0.047
182
INF009 Inflammatory Spondylopathy 32 0.047
183
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.047
184
PLY150 Polykaryocytosis Inducer 20 0.047
185
RFR001 Refractory Plasma Cell Neoplasm 19 0.047
186
ERY007 Erythropoietin Polycythemia 14 0.047
187
INH014 Inherited Predisposition to Essential Thrombocythemia 8 0.047
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