Search results for Baricitinib

83 hits were found for Baricitinib

# Family MCID Name MIFTS Score
1
P RHM011 Rheumatoid Arthritis 82 0.397
2
P ART022 Arthritis 71 0.381
3
P DRM053 Dermatitis, Atopic 68 0.266
4
DRM006 Dermatitis 63 0.260
5
ADL002 Adult Syndrome 62 0.241
6
c DRM054 Dermatitis, Atopic, 2 45 0.241
7
c SYS001 Systemic Lupus Erythematosus 88 0.212
8
P LPS004 Lupus Erythematosus 62 0.212
9
HRP004 Herpes Zoster 58 0.180
10
c SYS043 Systemic Lupus Erythematosus 1 39 0.161
11
SKN016 Skin Disease 64 0.127
12
P PSR002 Psoriasis 63 0.127
13
ATM095 Autoimmune Disease 62 0.127
14
P ALP009 Alopecia Areata 61 0.127
15
P ALP008 Alopecia 58 0.127
16
PST011 Pustulosis of Palm and Sole 51 0.127
17
c SPN225 Spondyloarthropathy 1 74 0.114
18
P TMP003 Temporal Arteritis 68 0.114
19
c JVN010 Juvenile Rheumatoid Arthritis 67 0.114
20
PSR001 Psoriatic Arthritis 63 0.114
21
c PSR017 Psoriasis 2 55 0.114
22
c PSR023 Psoriasis 1 50 0.114
23
c RHM021 Rheumatoid Arthritis, Systemic Juvenile 49 0.114
24
c PSR028 Psoriasis 7 40 0.114
25
c PSR018 Psoriasis 13 40 0.114
26
c PSR032 Psoriasis 11 40 0.114
27
PSR016 Psoriatic Juvenile Idiopathic Arthritis 39 0.114
28
P PLY187 Polyarticular Juvenile Idiopathic Arthritis 36 0.114
31
PCR003 Pauciarticular Onset Juvenile Idiopathic Arthritis 12 0.114
32
P KDN018 Kidney Disease 73 0.098
33
P GRF003 Graft-Versus-Host Disease 71 0.098
34
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.098
35
P DRM010 Dermatomyositis 62 0.098
36
CHL028 Childhood Type Dermatomyositis 55 0.098
37
HMT018 Hematopoietic Stem Cell Transplantation 54 0.098
38
c ACR116 Aicardi-Goutieres Syndrome 1 53 0.098
39
CYT002 Cytokine Deficiency 46 0.098
40
P STN012 Sting-Associated Vasculopathy, Infantile-Onset 40 0.098
41
CRP033 Corpus Callosum, Agenesis of, with Abnormal Genitalia 39 0.098
42
ATM052 Autoimmune Disease 1 38 0.098
43
c STN011 Sting-Associated Vasculopathy with Onset in Infancy 27 0.098
44
P LVR013 Liver Disease 71 0.080
45
DWN001 Down Syndrome 70 0.080
46
LVR012 Liver Cirrhosis 67 0.080
47
P SKN015 Skin Carcinoma 67 0.080
48
ALL026 Allergic Hypersensitivity Disease 65 0.080
49
FCT007 Factor Vii Deficiency 65 0.080
50
c RHB024 Rhabdomyosarcoma 2 64 0.080
51
P ENC018 Encephalopathy 64 0.080
52
P ACR001 Aicardi-Goutieres Syndrome 63 0.080
53
PLM033 Pulmonary Embolism 60 0.080
54
c DWL002 Dowling-Degos Disease 1 59 0.080
55
CNT047 Contact Dermatitis 58 0.080
56
PRM236 Primary Biliary Cholangitis 57 0.080
57
ALL010 Allergic Contact Dermatitis 56 0.080
58
c CHR417 Chronic Graft Versus Host Disease 56 0.080
59
SYN007 Synovitis 55 0.080
60
c MCR113 Microvascular Complications of Diabetes 3 55 0.080
61
P PRM006 Primary Biliary Cirrhosis 54 0.080
62
P CHL066 Cholangitis 53 0.080
63
c INF145 Infantile Liver Failure Syndrome 1 50 0.080
64
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.080
65
48X005 48,xyyy 37 0.080
66
CYT018 Cytochrome P450 2d6 Variant 28 0.080
67
HML018 Homologous Wasting Disease 22 0.080
68
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.057
69
P VSC007 Vascular Disease 65 0.057
70
BLL006 Bullous Pemphigoid 63 0.057
71
TTN003 Tetanus 62 0.057
72
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 62 0.057
73
c SCL052 Scleroderma, Familial Progressive 62 0.057
74
BND020 Bone Disease 60 0.057
75
GST045 Gastroenteritis 60 0.057
76
ADL030 Adult-Onset Still's Disease 59 0.057
77
P EXN002 Exanthem 58 0.057
78
OCL020 Ocular Cicatricial Pemphigoid 55 0.057
79
THR004 Thrombocytosis 52 0.057
80
BNN003 Bone Inflammation Disease 51 0.057
81
P CTN003 Cutaneous Lupus Erythematosus 50 0.057
82
MLL001 Molluscum Contagiosum 49 0.057
83
PRN035 Perniosis 28 0.057
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