Search results for "megakaryoblastic leukemia"

The MalaCard for "megakaryoblastic leukemia" has been retired.
Searching MalaCards for entries containing "megakaryoblastic leukemia"

71 hits were found for 'megakaryoblastic leukemia'

# Family MCID Name MIFTS Score
1
MGK001 Megakaryocytic Leukemia 55 8.533
2
MGK005 Megakaryoblastic Acute Myeloid Leukemia with T(1;22)(p13;q13) 13 3.340
3
ACT186 Acute Megakaryoblastic Leukemia in Down Syndrome 14 2.713
4
LKM059 Leukemia, Megakaryoblastic, with or Without Down Syndrome, Somatic 26 2.668
5
ACT165 Acute Megakaryoblastic Leukemia Without Down Syndrome 14 2.651
6
P LKM002 Leukemia 71 1.810
7
P MYL006 Myeloid Leukemia 66 0.782
8
P LYM026 Lymphoblastic Leukemia 62 0.571
9
c ACT073 Acute Leukemia 60 0.545
10
c LKM061 Leukemia, Acute Myeloid 73 0.424
11
c CHR064 Chronic Monocytic Leukemia 42 0.386
12
ACT118 Acute Non Lymphoblastic Leukemia 30 0.374
13
P LYM118 Lymphoma 69 0.368
14
LYM067 Lymphoid Leukemia 44 0.347
15
BNM001 Bone Marrow Cancer 51 0.330
16
DWN001 Down Syndrome 66 0.323
17
CHL061 Childhood Leukemia 49 0.312
18
MYL009 Myelodysplastic Syndrome 73 0.309
19
MRG013 Mirage Syndrome 29 0.296
20
PRM243 Primary Bone Cancer 29 0.284
21
c ACT020 Acute T Cell Leukemia 35 0.251
22
BNC003 Bone Cancer 58 0.248
23
MYL031 Myeloproliferative Neoplasm 58 0.238
24
c ADL001 Adult Lymphoma 39 0.229
25
LYM019 Lymphosarcoma 53 0.219
26
P MYL005 Myelofibrosis 67 0.210
27
RFR004 Refractory Hematologic Cancer 28 0.198
28
BNL002 Bone Lymphoma 32 0.193
29
ACT098 Acute Erythroid Leukemia 47 0.180
30
SRC014 Sarcoma 66 0.177
31
PRM151 Primary Bone Lymphoma 26 0.173
32
ADL002 Adult Syndrome 52 0.167
33
ACT113 Acute Myeloblastic Leukemia with Maturation 37 0.167
34
ACT114 Acute Myeloblastic Leukemia Without Maturation 29 0.166
35
RFR010 Refractory Anemia 45 0.158
36
MYL003 Myeloid Sarcoma 48 0.145
37
BLD053 Blood Platelet Disease 46 0.141
38
KDS001 Kid Syndrome 53 0.138
39
CHL071 Child Syndrome 58 0.138
40
END072 Endotheliitis 42 0.130
41
P THR014 Thrombocytopenia 64 0.116
42
ALN001 Aland Island Eye Disease 45 0.113
43
THR004 Thrombocytosis 55 0.112
44
P ESS003 Essential Thrombocythemia 70 0.105
45
P PLY018 Polycythemia 58 0.102
46
c RTN162 Retinitis Pigmentosa 2 48 0.096
47
P HPT023 Hepatocellular Carcinoma 92 0.093
48
DSS009 Disseminated Intravascular Coagulation 51 0.092
49
P PNC001 Pancytopenia 52 0.090
50
TTR021 Tetrasomy 21 20 0.090
51
RBR001 Roberts Syndrome 60 0.086
52
GNG013 Gingivitis 61 0.082
53
ACT176 Acute Panmyelosis with Myelofibrosis 19 0.081
54
NRN002 Neuronitis 41 0.078
55
KLN001 Klinefelter's Syndrome 50 0.070
56
CRD119 Cardiac Arrest 61 0.066
57
P DMN001 Diamond-Blackfan Anemia 69 0.064
58
BNF002 Bone Fracture 50 0.064
59
P RTT002 Rett Syndrome 77 0.063
60
GNG006 Gingival Hypertrophy 32 0.063
61
DCH001 Duchenne Muscular Dystrophy 79 0.061
62
P CRN211 Coronary Artery Disease 74 0.059
63
ART111 Artery Disease 55 0.057
64
BCK001 Becker Muscular Dystrophy 69 0.052
65
GLY014 Glycerol Kinase Deficiency 44 0.052
66
ADR026 Adrenal Hypoplasia, Congenital, with Hypogonadotropic Hypogonadism 38 0.052
67
c HRD015 Hereditary Night Blindness 36 0.052
68
P XLN012 X-Linked Congenital Stationary Night Blindness 29 0.052
69
c NGH018 Night Blindness, Congenital Stationary , 1e, Autosomal Recessive 27 0.052
70
CHR387 Chromosome Xp21 Deletion Syndrome 27 0.052
71
MYL053 Myeloid Proliferations Related to Down Syndrome 3 0.052