Search results for bosutinib

102 hits were found for bosutinib

# Family MCID Name MIFTS Score
1
P MYL006 Myeloid Leukemia 61 0.500
2
c LKM063 Leukemia, Chronic Myeloid 74 0.440
3
P LKM002 Leukemia 69 0.399
4
c CHR064 Chronic Monocytic Leukemia 43 0.306
5
P BRS047 Breast Cancer 99 0.213
6
P EXN002 Exanthem 58 0.177
7
P DRR001 Diarrhea 55 0.169
8
P KDN018 Kidney Disease 73 0.160
9
P TRN020 Turner Syndrome 66 0.151
10
P LKM062 Leukemia, Acute Lymphoblastic 68 0.141
11
ADL002 Adult Syndrome 62 0.141
12
P LYM031 Lymphocytic Leukemia 56 0.141
13
GLB002 Glioblastoma 74 0.131
14
GLB015 Glioblastoma Multiforme 60 0.131
15
P PNC035 Pancreatic Cancer 86 0.119
16
c CHR684 Chronic Kidney Disease 68 0.119
17
P NTR004 Neutropenia 64 0.119
18
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.119
19
c ACT071 Acute Kidney Failure 60 0.119
20
END030 End Stage Renal Failure 60 0.119
21
P GLM040 Glioma Susceptibility 1 68 0.107
22
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.107
23
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.107
24
P PLY014 Polycystic Kidney Disease 61 0.107
25
P CLR023 Colorectal Cancer 100 0.092
26
P LNG032 Lung Cancer 99 0.092
27
DWN001 Down Syndrome 70 0.092
28
P LYM118 Lymphoma 70 0.092
29
P PLM037 Pulmonary Hypertension 69 0.092
30
CHL065 Cholangiocarcinoma 68 0.092
31
P DMN002 Dementia 68 0.092
32
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.092
33
P ADN016 Adenocarcinoma 65 0.092
34
KHL003 Kohlschutter-Tonz Syndrome 63 0.092
35
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 61 0.092
36
INT079 Intrahepatic Cholangiocarcinoma 54 0.092
37
LYM019 Lymphosarcoma 48 0.092
38
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.075
39
P BLD134 Bladder Cancer 79 0.075
40
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.075
41
CRV035 Cervical Cancer 77 0.075
42
BRN028 Brain Cancer 75 0.075
43
P LVR013 Liver Disease 71 0.075
44
PNC129 Pancreatic Adenocarcinoma 69 0.075
45
P PLM036 Pulmonary Fibrosis 66 0.075
46
DMN031 Dementia, Lewy Body 66 0.075
47
IDP011 Idiopathic Interstitial Pneumonia 65 0.075
48
P THY023 Thymoma 64 0.075
49
LPD008 Lipid Metabolism Disorder 64 0.075
50
c SYS004 Systemic Mastocytosis 63 0.075
51
P MST009 Mastocytosis 62 0.075
52
c MST023 Mesothelioma, Malignant 59 0.075
53
SPN041 Spinal Cord Disease 57 0.075
54
c THY107 Thymoma, Familial 55 0.075
55
THY025 Thymus Cancer 55 0.075
56
LYM040 Lymphoblastic Lymphoma 54 0.075
57
c LRG017 Large Intestine Cancer 53 0.075
58
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.075
59
P BNG032 Benign Mesothelioma 47 0.075
60
MRG013 Mirage Syndrome 42 0.075
61
NSP002 Nasopharyngitis 41 0.075
62
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 28 0.075
63
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.075
64
P PRS040 Prostate Cancer 97 0.053
65
P ALZ034 Alzheimer Disease 90 0.053
66
MYL069 Myeloma, Multiple 85 0.053
67
P LNG064 Lung Cancer Susceptibility 3 79 0.053
68
P PRK057 Parkinson Disease, Late-Onset 77 0.053
69
c HYP836 Hypercholesterolemia, Familial, 1 74 0.053
70
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.053
71
P EPL164 Epilepsy 73 0.053
72
P GRF003 Graft-Versus-Host Disease 71 0.053
73
FRN006 Frontotemporal Dementia 70 0.053
74
P HYD006 Hydrocephalus 68 0.053
75
P THR014 Thrombocytopenia 67 0.053
76
c SML038 Small Cell Cancer of the Lung 67 0.053
77
MYL031 Myeloproliferative Neoplasm 66 0.053
78
P NRB010 Neuroblastoma 1 66 0.053
79
ACT119 Acute Promyelocytic Leukemia 63 0.053
80
LNG099 Lung Disease 62 0.053
81
c SCL052 Scleroderma, Familial Progressive 62 0.053
82
INT066 Interstitial Lung Disease 61 0.053
83
c ACT073 Acute Leukemia 59 0.053
84
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.053
85
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.053
86
P GST044 Gastritis 58 0.053
87
BRN004 Brain Edema 57 0.053
88
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 56 0.053
89
c CHR417 Chronic Graft Versus Host Disease 56 0.053
90
P SBS003 Substance Abuse 56 0.053
91
c CNG216 Congenital Hydrocephalus 55 0.053
92
SLC006 Silicosis 55 0.053
93
HMT018 Hematopoietic Stem Cell Transplantation 54 0.053
94
BNR002 Bone Resorption Disease 51 0.053
95
DDN006 Duodenitis 44 0.053
96
DVR002 Diverticulitis 44 0.053
97
c PCH010 Pachyonychia Congenita 3 43 0.053
99
48X005 48,xyyy 37 0.053
101
c DRR018 Diarrhea 9 28 0.053
102
BNG077 Benign Idiopathic Neonatal Seizures 27 0.053
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