Search results for Acalabrutinib

103 hits were found for Acalabrutinib

# Family MCID Name MIFTS Score
1
P LYM118 Lymphoma 68 0.446
2
LYM019 Lymphosarcoma 46 0.421
3
P LKM071 Leukemia, Chronic Lymphocytic 79 0.418
4
MNT001 Mantle Cell Lymphoma 69 0.365
5
P LKM002 Leukemia 68 0.337
6
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.316
7
LYM133 Lymphoma, Hodgkin, Classic 69 0.273
8
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.263
9
P BCL017 B-Cell Lymphoma 58 0.263
10
DFF005 Diffuse Large B-Cell Lymphoma 55 0.235
11
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.210
12
CLL014 Cll/sll 45 0.190
13
c PRM038 Primary Agammaglobulinemia 44 0.190
14
RTC005 Reticulosarcoma 47 0.182
15
DWN001 Down Syndrome 70 0.166
16
c RHB024 Rhabdomyosarcoma 2 67 0.166
17
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.166
18
P NTR004 Neutropenia 63 0.149
19
MCR004 Macroglobulinemia 49 0.149
20
FCT007 Factor Vii Deficiency 67 0.139
21
HMT002 Hematologic Cancer 62 0.129
22
MRG003 Marginal Zone B-Cell Lymphoma 52 0.129
23
P THR014 Thrombocytopenia 67 0.118
24
WLD007 Waldenstroem's Macroglobulinemia 61 0.118
25
LYM012 Lymphoplasmacytic Lymphoma 47 0.118
26
MYL069 Myeloma, Multiple 85 0.105
27
ADL002 Adult Syndrome 70 0.105
28
P LVR013 Liver Disease 68 0.105
29
P PNM007 Pneumonia 68 0.105
30
P FLL037 Follicular Lymphoma 67 0.105
31
PLS009 Plasma Cell Neoplasm 51 0.105
32
c INF145 Infantile Liver Failure Syndrome 1 50 0.105
33
c FLL041 Follicular Lymphoma 1 49 0.105
34
RCH001 Richter's Syndrome 45 0.105
35
CVD001 Covid-19 44 0.105
36
CYT002 Cytokine Deficiency 42 0.105
37
P RHM011 Rheumatoid Arthritis 80 0.091
38
P ART022 Arthritis 69 0.091
39
P TRN020 Turner Syndrome 67 0.091
40
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.091
41
P DRR001 Diarrhea 55 0.091
42
48X005 48,xyyy 39 0.091
43
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.091
44
LVR006 Liver Lymphoma 27 0.091
45
P OVR042 Ovarian Cancer 88 0.074
46
P ATX030 Ataxia-Telangiectasia 82 0.074
47
STR067 Stroke, Ischemic 81 0.074
48
P GRF003 Graft-Versus-Host Disease 72 0.074
49
DFC004 Deficiency Anemia 70 0.074
50
P HPT021 Hepatitis 67 0.074
51
BRK010 Burkitt Lymphoma 67 0.074
52
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.074
53
P SKN015 Skin Carcinoma 66 0.074
54
P ATR011 Atrial Fibrillation 66 0.074
55
c FML001 Familial Atrial Fibrillation 65 0.074
56
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.074
57
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.074
58
c HPT001 Hepatitis C 62 0.074
59
ALL026 Allergic Hypersensitivity Disease 62 0.074
60
c HPT016 Hepatitis B 59 0.074
61
P LYM033 Lymphoproliferative Syndrome 59 0.074
62
PRG009 Progressive Multifocal Leukoencephalopathy 59 0.074
63
c CHR417 Chronic Graft Versus Host Disease 57 0.074
64
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 57 0.074
65
ACT058 Active Peptic Ulcer Disease 55 0.074
66
HRY003 Hairy Cell Leukemia 55 0.074
67
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.074
68
PST046 Post-Transplant Lymphoproliferative Disease 53 0.074
69
TLN003 Telangiectasis 52 0.074
70
c CHR418 Chronic Leukemia 49 0.074
71
PRL017 Prolymphocytic Leukemia 47 0.074
72
c DRR009 Diarrhea 6 46 0.074
73
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.074
74
P PRM293 Primary Mediastinal B-Cell Lymphoma 43 0.074
75
ATX019 Ataxia with Vitamin E Deficiency 42 0.074
76
c OVR114 Ovarian Cancer 1 38 0.074
77
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 36 0.074
78
MNT320 Mental Retardation, Autosomal Dominant 6, with or Without Seizures 30 0.074
79
CLS052 Classic Hairy Cell Leukemia 27 0.074
80
c ATS386 Autosomal Dominant Non-Syndromic Intellectual Disability 4 25 0.074
81
HRP008 Herpes Simiae 25 0.074
82
CHR208 Chromosome 17p Deletion 23 0.074
83
c ATS388 Autosomal Dominant Non-Syndromic Intellectual Disability 6 23 0.074
84
AGG011 Aggressive B-Cell Non-Hodgkin Lymphoma 23 0.074
85
HML018 Homologous Wasting Disease 22 0.074
86
P LNG032 Lung Cancer 98 0.053
87
P PNC035 Pancreatic Cancer 84 0.053
88
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.053
89
IMM167 Immune Deficiency Disease 78 0.053
90
c SML038 Small Cell Cancer of the Lung 65 0.053
91
P AGM001 Agammaglobulinemia 65 0.053
92
P PRD008 Periodontitis 64 0.053
93
SQM006 Squamous Cell Carcinoma 60 0.053
94
P EXN002 Exanthem 57 0.053
95
CLL003 Cellulitis 54 0.053
96
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.053
97
BNR002 Bone Resorption Disease 48 0.053
98
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.053
99
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.053
100
SYN036 Syncope 45 0.053
101
IMM136 Immune System Disease 45 0.053
102
P HYP073 Hypersensitivity Reaction Type Iv Disease 44 0.053
103
TMR016 Tumor Suppressor Gene on Chromosome 11 28 0.053
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