Search results for "megakaryoblastic leukemia"

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

81 hits were found for 'megakaryoblastic leukemia'

# Family MCID Name MIFTS Score
1
MGK001 Megakaryocytic Leukemia 53 8.527
2
MGK005 Megakaryoblastic Acute Myeloid Leukemia with T(1;22)(p13;q13) 12 3.331
3
ACT186 Acute Megakaryoblastic Leukemia in Down Syndrome 14 2.723
4
ACT165 Acute Megakaryoblastic Leukemia Without Down Syndrome 13 2.644
5
LKM059 Leukemia, Megakaryoblastic, with or Without Down Syndrome, Somatic 13 2.586
6
P LKM002 Leukemia 70 1.818
7
P MYL006 Myeloid Leukemia 67 0.789
8
P LYM026 Lymphoblastic Leukemia 60 0.580
9
c ACT073 Acute Leukemia 61 0.550
10
c LKM061 Leukemia, Acute Myeloid 71 0.415
11
P LYM118 Lymphoma 68 0.387
12
c CHR064 Chronic Monocytic Leukemia 42 0.387
13
ACT118 Acute Non Lymphoblastic Leukemia 27 0.375
14
LYM067 Lymphoid Leukemia 38 0.351
15
CHL061 Childhood Leukemia 47 0.341
16
BNM001 Bone Marrow Cancer 56 0.332
17
DWN001 Down Syndrome 65 0.326
18
SPN041 Spinal Cord Disease 50 0.305
19
MYL009 Myelodysplastic Syndrome 73 0.300
20
P MNC007 Monocytic Leukemia 52 0.276
21
BNC003 Bone Cancer 44 0.273
22
c ACT020 Acute T Cell Leukemia 38 0.253
23
c ADL001 Adult Lymphoma 40 0.248
24
LYM019 Lymphosarcoma 52 0.239
25
c CHR092 Chronic Myeloproliferative Disease 50 0.237
26
TNP003 Tn Polyagglutination Syndrome, Somatic 30 0.232
27
P MYL005 Myelofibrosis 67 0.214
28
RFR004 Refractory Hematologic Cancer 27 0.196
29
BNL002 Bone Lymphoma 34 0.194
30
SRC014 Sarcoma 66 0.183
31
ACT098 Acute Erythroid Leukemia 34 0.182
32
ADL002 Adult Syndrome 53 0.182
33
PRM151 Primary Bone Lymphoma 26 0.172
34
ACT113 Acute Myeloblastic Leukemia with Maturation 40 0.170
35
ACT114 Acute Myeloblastic Leukemia Without Maturation 29 0.168
36
RFR010 Refractory Anemia 43 0.163
37
MYL003 Myeloid Sarcoma 48 0.150
38
BLD053 Blood Platelet Disease 44 0.142
39
ALN001 Aland Island Eye Disease 45 0.141
40
CHL071 Child Syndrome 58 0.139
41
KDS001 Kid Syndrome 53 0.139
42
END072 Endotheliitis 41 0.135
43
MGK002 Megakaryocytic Tumor 32 0.133
44
P THR014 Thrombocytopenia 63 0.122
45
THR004 Thrombocytosis 55 0.114
46
c RTN162 Retinitis Pigmentosa 2 50 0.110
47
P ESS003 Essential Thrombocythemia 66 0.108
48
P PLY018 Polycythemia 58 0.108
49
c ACT195 Acute Myeloid Leukemia with T(9;11)(p22;q23) 24 0.106
50
DSS009 Disseminated Intravascular Coagulation 52 0.099
51
HPT023 Hepatocellular Carcinoma 90 0.095
52
P PNC001 Pancytopenia 53 0.095
53
MYL055 Myeloid/lymphoid or Mixed Lineage Leukemia 29 0.092
54
TTR021 Tetrasomy 21 20 0.091
55
GNG013 Gingivitis 61 0.089
56
EMN001 Emanuel Syndrome 38 0.089
57
LKM001 Leukemoid Reaction 46 0.087
58
RBR001 Roberts Syndrome 61 0.086
59
DCH001 Duchenne Muscular Dystrophy 81 0.083
60
ACT176 Acute Panmyelosis with Myelofibrosis 19 0.082
61
NRN002 Neuronitis 40 0.080
62
c HRD015 Hereditary Night Blindness 39 0.076
63
c NGH018 Night Blindness, Congenital Stationary , 1e, Autosomal Recessive 26 0.076
64
P XLN012 X-Linked Congenital Stationary Night Blindness 25 0.076
65
BCK001 Becker Muscular Dystrophy 68 0.074
66
KLN001 Klinefelter's Syndrome 52 0.071
67
GLY014 Glycerol Kinase Deficiency 46 0.071
68
ADR026 Adrenal Hypoplasia, Congenital, with Hypogonadotropic Hypogonadism 36 0.071
69
CNR028 Cone-Rod Dystropy, X-Linked, 3 23 0.071
70
c NGH020 Night Blindness, Congenital Stationary , 2a, X-Linked 24 0.071
71
P NGH001 Night Blindness 49 0.071
72
CHR387 Chromosome Xp21 Deletion Syndrome 27 0.071
73
NNS032 Non-Syndromic X-Linked Intellectual Disability 30 0.071
74
PNL002 Pineal Parenchymal Tumor of Intermediate Differentiation 29 0.071
75
P RTT002 Rett Syndrome 77 0.068
76
CRD119 Cardiac Arrest 63 0.067
77
GNG006 Gingival Hypertrophy 29 0.064
78
BNF002 Bone Fracture 46 0.064
79
P CRN211 Coronary Artery Disease 74 0.063
80
P DMN001 Diamond-Blackfan Anemia 69 0.063
81
ART111 Artery Disease 56 0.058