Search results for "thrombocythemia 2"

The MalaCard for "thrombocythemia 2" has been retired.
Searching MalaCards for entries containing "thrombocythemia 2"

256 hits were found for 'thrombocythemia 2'

# Family MCID Name MIFTS Score
1
P ESS003 Essential Thrombocythemia 68 0.814
2
P PLY018 Polycythemia 57 0.451
3
P MYL005 Myelofibrosis 67 0.345
4
P LKM002 Leukemia 70 0.277
5
THR004 Thrombocytosis 55 0.238
6
END072 Endotheliitis 42 0.219
7
BLD053 Blood Platelet Disease 46 0.214
8
P HMR003 Hemorrhagic Disease 57 0.204
9
BNM001 Bone Marrow Cancer 52 0.203
10
P BLD051 Blood Coagulation Disease 45 0.200
11
MRG013 Mirage Syndrome 26 0.200
12
TNP003 Tn Polyagglutination Syndrome, Somatic 44 0.200
13
VSC008 Vascular Hemostatic Disease 33 0.199
14
c THR090 Thrombocythemia 1 34 0.192
15
P MYC007 Myocardial Infarction 79 0.191
16
CMP005 Campomelic Dysplasia 72 0.188
17
P LYM118 Lymphoma 70 0.170
18
c THR086 Thrombocythemia 3 28 0.166
19
PLY125 Polycythemia Vera, Somatic 63 0.165
20
c PRM012 Primary Polycythemia 51 0.165
21
c HMG001 Hemoglobin C Disease 47 0.165
22
P MYL006 Myeloid Leukemia 67 0.161
23
CRB009 Cerebritis 38 0.151
24
P LNG032 Lung Cancer 94 0.133
25
P HPT021 Hepatitis 70 0.129
26
P HRT032 Heart Disease 76 0.127
27
BNC003 Bone Cancer 45 0.127
28
RTN023 Retinitis 49 0.126
29
P MLT019 Multiple Myeloma 80 0.126
30
c ACT075 Acute Myocardial Infarction 60 0.125
31
SPL012 Splenic Disease 47 0.121
32
BNS002 Bone Structure Disease 36 0.115
33
WTH001 Withdrawal Disorder 41 0.115
34
HMT002 Hematologic Cancer 64 0.113
35
ALR002 Al-Raqad Syndrome 36 0.111
36
SRC014 Sarcoma 66 0.111
37
ATH003 Atherosclerosis 62 0.109
38
ADJ001 Adjustment Disorder 38 0.109
39
DFC004 Deficiency Anemia 65 0.107
40
MYL009 Myelodysplastic Syndrome 74 0.106
41
c CHR090 Chronic Lymphocytic Leukemia 74 0.105
42
ISC004 Ischemia 59 0.105
43
P RNL014 Renal Cell Carcinoma 81 0.104
44
P ART022 Arthritis 75 0.104
45
SPL018 Splenomegaly 44 0.101
46
c MYC058 Myocardial Infarction 2 29 0.097
47
c ACT073 Acute Leukemia 62 0.096
48
P CRD011 Cardiomyopathy 67 0.095
49
c HPT001 Hepatitis C 68 0.093
50
P RHM011 Rheumatoid Arthritis 88 0.093
51
HPT023 Hepatocellular Carcinoma 91 0.092
52
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 41 0.091
53
PRP027 Peripheral Vascular Disease 69 0.090
54
CRN017 Coronary Thrombosis 48 0.090
55
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.088
56
BLD054 Blood Protein Disease 40 0.088
57
c HMG004 Hemoglobin D Disease 33 0.087
58
ANR040 Aneurysm 57 0.086
59
P THR014 Thrombocytopenia 64 0.085
60
STM006 Stomach Disease 50 0.085
61
c BLD124 Bleeding Disorder, Platelet-Type, 11 42 0.085
62
QBC001 Quebec Platelet Disorder 50 0.084
63
c THR092 Thrombophilia Due to Thrombin Defect 56 0.084
64
P BDD001 Budd-Chiari Syndrome 56 0.083
65
PRP021 Peripheral Nervous System Neoplasm 50 0.083
66
PCK002 Pick Disease 67 0.083
67
SPL011 Spleen Cancer 37 0.081
68
ORL011 Oral Cancer 55 0.081
69
HRY003 Hairy Cell Leukemia 60 0.080
70
c CRN214 Coronary Heart Disease 5 23 0.080
71
RFR010 Refractory Anemia 45 0.080
72
BRT030 Birth Defects 43 0.079
73
c HPT003 Hepatitis a 59 0.079
74
ACR041 Acromelic Frontonasal Dysostosis 46 0.079
75
LYM019 Lymphosarcoma 53 0.078
76
c ADL001 Adult Lymphoma 41 0.077
77
c LKM061 Leukemia, Acute Myeloid 71 0.077
78
CLL008 Cellular Phase Chronic Idiopathic Myelofibrosis 17 0.077
79
P ORL007 Oral Cavity Cancer 58 0.076
80
c HPT016 Hepatitis B 64 0.076
81
P THR015 Thrombophilia 59 0.076
82
LKC003 Leukocyte Disease 47 0.075
83
HDG012 Hodgkin Lymphoma 73 0.074
84
CTS003 Coats Disease 57 0.074
85
c MCL062 Mucolipidosis Ii Alpha/beta 60 0.073
86
PHY001 Physiological Polycythemia 31 0.072
87
HRT007 Heart Cancer 50 0.072
88
HMT018 Hematopoietic Stem Cell Transplantation 41 0.072
89
P HRT017 Heart Tumor 35 0.072
90
c ADL079 Adult Heart Tumor 19 0.072
91
P APL001 Aplastic Anemia 73 0.072
92
FRB001 Farber Lipogranulomatosis 51 0.071
93
BND014 Bone Development Disease 42 0.071
94
VND001 Vein Disease 52 0.071
95
DRG003 Drug Dependence 53 0.071
96
ACR002 Acrocapitofemoral Dysplasia 36 0.070
97
PRP030 Purpura 59 0.069
98
SNS023 Sensory System Cancer 46 0.068
99
ANG054 Angina Pectoris 51 0.068
100
CRD118 Cardiovascular Cancer 47 0.068
101
AND005 Androgen Insensitivity Syndrome, Mild 16 0.067
102
ALP008 Alopecia 55 0.067
103
MGK001 Megakaryocytic Leukemia 53 0.066
104
SPC003 Specific Developmental Disorder 40 0.066
105
P INF032 Infertility 61 0.066
106
P PLM037 Pulmonary Hypertension 79 0.066
107
HPT074 Hepatic Adenoma, Somatic 51 0.066
108
P LKM068 Leukemia, Chronic Myeloid, Somatic 66 0.065
109
ACD009 Acid-Labile Subunit, Deficiency of 48 0.065
110
HNM002 Hinman Syndrome 25 0.065
111
c CHR064 Chronic Monocytic Leukemia 43 0.064
112
VNW001 Von Willebrand's Disease 61 0.064
113
PRD011 Proud Syndrome 42 0.064
114
ACT118 Acute Non Lymphoblastic Leukemia 29 0.064
115
LPD004 Lipoid Nephrosis 48 0.064
116
IMM127 Immune System Cancer 42 0.063
117
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 36 0.063
118
MND006 Mondor Disease 21 0.063
119
P DRR001 Diarrhea 51 0.063
120
ACQ017 Acquired Von Willebrand Syndrome 36 0.063
121
CHR008 Choroiditis 43 0.063
122
P CHR084 Chromosomal Disease 37 0.063
123
P HMP007 Hemophilia 56 0.063
124
SPN051 Spondylitis 50 0.062
125
c CHR418 Chronic Leukemia 48 0.062
126
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.062
127
CGL001 Coagulation Protein Disease 16 0.062
128
PRP016 Paraplegia 49 0.062
129
ANG049 Angioedema Induced by Ace Inhibitors 35 0.061
130
MLG108 Malignant Melanoma, Somatic 67 0.061
131
P SPN301 Spinocerebellar Ataxia 2 63 0.061
132
CHR285 Chronic Myelomonocytic Leukemia 55 0.061
133
RFR004 Refractory Hematologic Cancer 29 0.060
134
HYP037 Hyperhomocysteinemia 50 0.060
135
ACT095 Acute Biphenotypic Leukemia 33 0.060
136
HPR003 Heparin-Induced Thrombocytopenia 46 0.060
137
c HMP029 Hemophilia a 64 0.060
138
ALN001 Aland Island Eye Disease 45 0.059
139
VSC006 Vascular Cancer 54 0.059
140
P MST009 Mastocytosis 54 0.058
141
MYL004 Myelodysplastic Myeloproliferative Cancer 47 0.058
142
CNT098 Central Core Disease 66 0.057
143
LNS003 Lens Disease 38 0.057
144
PLS009 Plasma Cell Neoplasm 48 0.057
145
c DLT002 Dilated Cardiomyopathy 75 0.057
146
GLM011 Glomerulosclerosis 44 0.056
147
OCL009 Ocular Cancer 62 0.055
148
MYC006 Mycosis Fungoides 66 0.055
149
c SYS004 Systemic Mastocytosis 59 0.054
150
MYL003 Myeloid Sarcoma 48 0.054
151
BNL002 Bone Lymphoma 33 0.054
152
MYC002 Mycobacterium Avium Complex Disease 51 0.054
153
CRD001 Cardiac Tamponade 44 0.054
154
GST019 Gastrointestinal Stromal Tumor 72 0.053
155
PLM012 Pulmonary Sarcoidosis 54 0.052
156
P FCL005 Focal Segmental Glomerulosclerosis 59 0.052
157
CHL067 Cholecystitis 56 0.052
158
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.052
159
IRN001 Iron Deficiency Anemia 51 0.052
160
P RNV001 Renovascular Hypertension 47 0.052
161
CNT010 Central Nervous System Hematologic Cancer 21 0.052
162
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 44 0.050
163
P RTN022 Retinal Vein Occlusion 37 0.050
164
P NTR004 Neutropenia 59 0.050
165
c THR037 Thrombocytopenia 2 37 0.050
166
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.049
167
PRT018 Portal Vein Thrombosis 49 0.049
168
c ACQ014 Acquired Hemophilia 42 0.049
169
c ACQ042 Acquired Hemophilia a 39 0.049
170
c CNT016 Central Retinal Vein Occlusion 35 0.049
171
P SHR029 Short Syndrome 60 0.048
172
STR037 Stress Cardiomyopathy 36 0.048
173
CRD119 Cardiac Arrest 63 0.048
174
FXF002 Fox-Fordyce Disease 39 0.048
175
P ESN007 Eosinophilia 61 0.048
176
P HMR012 Hemorrhagic Fever 55 0.047
177
ALP001 Alopecia Universalis 57 0.047
178
ACR007 Acromegaly 65 0.046
179
P MSC007 Muscle Hypertrophy 59 0.046
180
PLS025 Plasmablastic Lymphoma 45 0.045
181
P RTN014 Retinal Artery Occlusion 43 0.045
182
LRG008 Large Granular Lymphocyte Leukemia 38 0.045
183
PRM151 Primary Bone Lymphoma 27 0.045
184
MGR028 Migraine with or Without Aura 1 50 0.045
185
CHY002 Chylomicron Retention Disease 59 0.044
186
c SRC023 Sarcoidosis 2 33 0.044
187
NVS001 Neovascular Glaucoma 43 0.044
188
IRN004 Iron-Refractory Iron Deficiency Anemia 38 0.044
189
MYL045 Myelofibrosis with Myeloid Metaplasia, Somatic 36 0.044
190
c CNT028 Central Retinal Artery Occlusion 35 0.044
191
P LMY004 Leiomyosarcoma 53 0.043
192
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 34 0.043
193
c SPN225 Spondyloarthropathy 1 63 0.042
194
P PNC001 Pancytopenia 52 0.042
195
SCT005 Scott Syndrome 50 0.042
196
P ERY048 Erythrocytosis, Familial, 2 42 0.042
197
P LFR001 Li-Fraumeni Syndrome 75 0.040
198
P PRP029 Porphyria 58 0.040
199
EWN002 Ewing's Family of Tumors 45 0.039
200
P CHR562 Chronic Myelocytic Leukemia 41 0.039
201
c DLT001 Delta Chain Disease 16 0.039
202
c PRM225 Primary Thrombocytopenia 42 0.039
203
c THR048 Thrombocytopenia 4 29 0.039
204
c SVR003 Severe Congenital Neutropenia 56 0.038
205
P HYP098 Hypereosinophilic Syndrome 51 0.038
206
PLS016 Plasma Cell Leukemia 42 0.038
207
c DRR009 Diarrhea 6 31 0.038
208
P DMN001 Diamond-Blackfan Anemia 68 0.037
209
ACT098 Acute Erythroid Leukemia 48 0.037
210
LYM051 Lymphomatoid Granulomatosis 46 0.037
211
P ARC016 Auriculocondylar Syndrome 1 44 0.037
212
CYC007 Cyclic Thrombocytopenia 37 0.037
213
CHR028 Chronic Wasting Disease 34 0.037
214
PRM053 Primary Release Disorder of Platelets 14 0.037
215
CRN073 Coronary Arteries Congenital Malformation 13 0.037
216
PGT001 Paget's Disease of Bone 59 0.035
217
PBL001 Piebaldism 57 0.035
218
ACR008 Acrocallosal Syndrome 51 0.035
219
FBR002 Fibrosarcoma of Bone 41 0.035
220
ACT113 Acute Myeloblastic Leukemia with Maturation 40 0.035
221
ALK015 Alk-Positive Anaplastic Large Cell Lymphoma 36 0.035
222
NNT011 Neonatal Anemia 34 0.035
223
c THR110 Thrombocytopenia 6 22 0.035
224
P PRP003 Porphyria Cutanea Tarda 64 0.034
225
MCK005 Mckusick-Kaufman Syndrome 52 0.034
226
P HYP237 Hypercalcemia, Infantile 51 0.034
227
HMR002 Hemarthrosis 48 0.034
228
MLT113 Multicentric Castleman Disease 47 0.034
229
FBR032 Fibromuscular Dysplasia 45 0.034
230
SND002 Sneddon Syndrome 44 0.034
231
ANM001 Anemia of Prematurity 43 0.034
232
HYP458 Hyper Ige Syndrome 41 0.034
233
CRN055 Carney Triad 39 0.034
234
URT008 Urticaria Pigmentosa 38 0.034
235
CST005 Castleman Disease 38 0.034
236
AMR003 Amaurosis Fugax 38 0.034
237
c ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 35 0.034
238
P PSR004 Psoriasis Susceptibility 1 33 0.034
239
LKM066 Leukemia, Acute Myelomonocytic, Somatic, Somatic 62 0.032
240
MNK001 Menkes Disease 61 0.032
241
PRP032 Porphyria Variegata 52 0.032
242
MST017 Mast Cell Disease 52 0.032
243
CHR563 Chronic Eosinophilic Leukemia 47 0.032
244
MST001 Mast-Cell Sarcoma 46 0.032
245
NTR018 Neutrophilia, Hereditary 45 0.032
246
c NTR038 Neutropenia, Severe Congenital 3, Autosomal Recessive 41 0.032
247
LNG013 Lung Lymphoma 40 0.032
248
ERY045 Erythrocytosis, Somatic 35 0.032
249
SPN060 Spondylocarpotarsal Synostosis Syndrome 35 0.032
250
TRN030 Transient Erythroblastopenia of Childhood 33 0.032
251
HRT003 Heart Lymphoma 31 0.032
252
c ACQ010 Acquired Polycythemia 31 0.032
253
SQM005 Squamous Papillomatosis 31 0.032
254
FLS001 Fils Syndrome 28 0.032
255
VSC001 Vascular Myelopathy 25 0.032
256
PNG002 Pain Agnosia 25 0.032