Search results for "megakaryoblastic leukemia"

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

76 hits were found for 'megakaryoblastic leukemia'

# Family MCID Name MIFTS Score
1
MGK001 Megakaryocytic Leukemia 53 8.538
2
MGK005 Megakaryoblastic Acute Myeloid Leukemia with T(1;22)(p13;q13) 13 3.335
3
ACT186 Acute Megakaryoblastic Leukemia in Down Syndrome 15 2.709
4
LKM059 Leukemia, Megakaryoblastic, with or Without Down Syndrome, Somatic 26 2.666
5
ACT165 Acute Megakaryoblastic Leukemia Without Down Syndrome 14 2.648
6
P LKM002 Leukemia 70 1.831
7
P MYL006 Myeloid Leukemia 67 0.788
8
P LYM026 Lymphoblastic Leukemia 60 0.585
9
c ACT073 Acute Leukemia 62 0.555
10
c LKM061 Leukemia, Acute Myeloid 71 0.419
11
c CHR064 Chronic Monocytic Leukemia 43 0.392
12
P LYM118 Lymphoma 70 0.390
13
ACT118 Acute Non Lymphoblastic Leukemia 29 0.380
14
LYM067 Lymphoid Leukemia 43 0.354
15
BNM001 Bone Marrow Cancer 52 0.336
16
CHL061 Childhood Leukemia 48 0.333
17
DWN001 Down Syndrome 65 0.319
18
MRG013 Mirage Syndrome 26 0.305
19
MYL009 Myelodysplastic Syndrome 74 0.300
20
BNC003 Bone Cancer 45 0.262
21
c ACT020 Acute T Cell Leukemia 39 0.255
22
LYM019 Lymphosarcoma 53 0.243
23
CMP005 Campomelic Dysplasia 72 0.238
24
c ADL001 Adult Lymphoma 41 0.237
25
c ACT009 Acute Monocytic Leukemia 52 0.220
26
P MYL005 Myelofibrosis 67 0.211
27
RFR004 Refractory Hematologic Cancer 29 0.199
28
BNL002 Bone Lymphoma 33 0.195
29
ACT098 Acute Erythroid Leukemia 48 0.183
30
SRC014 Sarcoma 66 0.179
31
PRM151 Primary Bone Lymphoma 27 0.174
32
ADL002 Adult Syndrome 53 0.171
33
ACT113 Acute Myeloblastic Leukemia with Maturation 40 0.171
34
ACT114 Acute Myeloblastic Leukemia Without Maturation 30 0.170
35
RFR010 Refractory Anemia 45 0.161
36
MYL003 Myeloid Sarcoma 48 0.147
37
BLD053 Blood Platelet Disease 46 0.143
38
CHL071 Child Syndrome 58 0.140
39
KDS001 Kid Syndrome 53 0.140
40
END072 Endotheliitis 42 0.131
41
P THR014 Thrombocytopenia 64 0.117
42
ALN001 Aland Island Eye Disease 45 0.117
43
THR004 Thrombocytosis 55 0.112
44
P ESS003 Essential Thrombocythemia 68 0.105
45
P PLY018 Polycythemia 57 0.104
46
c RTN162 Retinitis Pigmentosa 2 51 0.095
47
HPT023 Hepatocellular Carcinoma 91 0.093
48
DSS009 Disseminated Intravascular Coagulation 51 0.093
49
P PNC001 Pancytopenia 52 0.090
50
TTR021 Tetrasomy 21 19 0.089
51
RBR001 Roberts Syndrome 59 0.086
52
GNG013 Gingivitis 60 0.083
53
c ACT195 Acute Myeloid Leukemia with T(9;11)(p22;q23) 23 0.083
54
ACT176 Acute Panmyelosis with Myelofibrosis 19 0.080
55
NRN002 Neuronitis 42 0.078
56
MYL055 Myeloid/lymphoid or Mixed Lineage Leukemia 30 0.072
57
KLN001 Klinefelter's Syndrome 55 0.071
58
BNF002 Bone Fracture 47 0.064
59
P DMN001 Diamond-Blackfan Anemia 68 0.062
60
CRD119 Cardiac Arrest 63 0.062
61
GNG006 Gingival Hypertrophy 32 0.062
62
P RTT002 Rett Syndrome 78 0.061
63
DCH001 Duchenne Muscular Dystrophy 80 0.059
64
P CRN211 Coronary Artery Disease 75 0.057
65
ART111 Artery Disease 57 0.057
66
c HRD015 Hereditary Night Blindness 40 0.054
67
c NGH019 Night Blindness, Congenital Stationary , 1a, X-Linked 35 0.054
68
P XLN012 X-Linked Congenital Stationary Night Blindness 26 0.054
69
c NGH018 Night Blindness, Congenital Stationary , 1e, Autosomal Recessive 26 0.054
70
BCK001 Becker Muscular Dystrophy 68 0.051
71
P NGH001 Night Blindness 49 0.051
72
GLY014 Glycerol Kinase Deficiency 45 0.051
73
ADR026 Adrenal Hypoplasia, Congenital, with Hypogonadotropic Hypogonadism 41 0.051
74
PNL002 Pineal Parenchymal Tumor of Intermediate Differentiation 31 0.051
75
CHR387 Chromosome Xp21 Deletion Syndrome 27 0.051
76
MYL053 Myeloid Proliferations Related to Down Syndrome 3 0.051