Search results for Baricitinib

132 hits were found for Baricitinib

# Family MCID Name MIFTS Score
1
P RHM011 Rheumatoid Arthritis 80 0.398
2
P ART022 Arthritis 69 0.380
3
CVD001 Covid-19 44 0.257
4
P DRM053 Dermatitis, Atopic 66 0.243
5
DRM006 Dermatitis 61 0.228
6
ADL002 Adult Syndrome 70 0.223
7
c DRM054 Dermatitis, Atopic, 2 44 0.206
8
c SYS001 Systemic Lupus Erythematosus 86 0.194
9
P LPS004 Lupus Erythematosus 61 0.194
10
c SVR001 Severe Acute Respiratory Syndrome 62 0.188
11
CYT002 Cytokine Deficiency 42 0.175
12
HRP004 Herpes Zoster 60 0.168
13
P PNM007 Pneumonia 68 0.146
14
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.137
15
c JVN010 Juvenile Rheumatoid Arthritis 64 0.137
16
c JVN061 Juvenile Arthritis 60 0.137
17
c SYS043 Systemic Lupus Erythematosus 1 38 0.137
18
P ALP009 Alopecia Areata 60 0.129
19
P ALP008 Alopecia 54 0.129
20
P PSR002 Psoriasis 62 0.119
21
PST011 Pustulosis of Palm and Sole 52 0.119
22
P GRF003 Graft-Versus-Host Disease 72 0.109
23
c RHB024 Rhabdomyosarcoma 2 67 0.109
24
SKN016 Skin Disease 63 0.109
25
c SPN225 Spondyloarthropathy 1 73 0.097
26
P TMP003 Temporal Arteritis 68 0.097
27
ATM095 Autoimmune Disease 62 0.097
28
ALL026 Allergic Hypersensitivity Disease 62 0.097
29
PSR001 Psoriatic Arthritis 61 0.097
30
VRL011 Viral Infectious Disease 61 0.097
31
PLM033 Pulmonary Embolism 59 0.097
32
P EXN002 Exanthem 57 0.097
33
c PSR017 Psoriasis 2 53 0.097
34
c PSR023 Psoriasis 1 52 0.097
35
c PSR032 Psoriasis 11 47 0.097
36
c STN011 Sting-Associated Vasculopathy with Onset in Infancy 45 0.097
37
c PSR028 Psoriasis 7 42 0.097
38
P STN012 Sting-Associated Vasculopathy, Infantile-Onset 42 0.097
39
c PSR018 Psoriasis 13 41 0.097
40
PSR016 Psoriatic Juvenile Idiopathic Arthritis 40 0.097
41
P PLY187 Polyarticular Juvenile Idiopathic Arthritis 37 0.097
44
HML018 Homologous Wasting Disease 22 0.097
45
PCR003 Pauciarticular Onset Juvenile Idiopathic Arthritis 12 0.097
46
P KDN018 Kidney Disease 72 0.084
47
P MYP004 Myopathy 70 0.084
48
P SKN015 Skin Carcinoma 66 0.084
49
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.084
50
P DRM010 Dermatomyositis 61 0.084
51
INC002 Inclusion Body Myositis 58 0.084
52
CHL028 Childhood Type Dermatomyositis 58 0.084
53
P MYS005 Myositis 56 0.084
54
c PRM038 Primary Agammaglobulinemia 44 0.084
55
DVR002 Diverticulitis 43 0.084
56
P OVR096 Overlap Myositis 27 0.084
57
P RSP003 Respiratory Failure 74 0.069
58
P LVR013 Liver Disease 68 0.069
59
P MYC084 Mycobacterium Tuberculosis 1 68 0.069
60
P LKM002 Leukemia 68 0.069
61
FCT007 Factor Vii Deficiency 67 0.069
62
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.069
63
P ADL010 Adult Respiratory Distress Syndrome 65 0.069
64
P ACR001 Aicardi-Goutieres Syndrome 62 0.069
65
P PRM006 Primary Biliary Cirrhosis 62 0.069
66
LVR012 Liver Cirrhosis 62 0.069
67
P ENC018 Encephalopathy 61 0.069
68
INT066 Interstitial Lung Disease 60 0.069
69
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.069
70
CNT047 Contact Dermatitis 58 0.069
71
c DWL002 Dowling-Degos Disease 1 58 0.069
72
P UVT001 Uveitis 57 0.069
73
c CHR417 Chronic Graft Versus Host Disease 57 0.069
74
THR024 Thrombosis 57 0.069
75
ALL010 Allergic Contact Dermatitis 56 0.069
76
SYN007 Synovitis 54 0.069
77
PLM010 Pulmonary Edema 54 0.069
78
c MCR113 Microvascular Complications of Diabetes 3 52 0.069
79
c ACR116 Aicardi-Goutieres Syndrome 1 52 0.069
80
c ACT135 Acute Graft Versus Host Disease 52 0.069
81
P CHL066 Cholangitis 51 0.069
82
c INF145 Infantile Liver Failure Syndrome 1 50 0.069
83
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 47 0.069
84
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.069
85
MDD018 Middle East Respiratory Syndrome 43 0.069
86
CRN322 Coronavirus Infectious Disease 40 0.069
87
CRP033 Corpus Callosum, Agenesis of, with Abnormal Genitalia 39 0.069
88
48X005 48,xyyy 39 0.069
89
c CHR682 Chronic Bilirubin Encephalopathy 39 0.069
90
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.069
91
ATM052 Autoimmune Disease 1 37 0.069
92
PLC002 Plica Syndrome 36 0.069
93
ENC065 Encephalitis/encephalopathy, Mild, with Reversible Myelin Vacuolization 33 0.069
94
CYT018 Cytochrome P450 2d6 Variant 27 0.069
95
P HRT032 Heart Disease 75 0.049
96
SVR004 Severe Combined Immunodeficiency 73 0.049
97
c HYP836 Hypercholesterolemia, Familial, 1 73 0.049
98
P SRC025 Sarcoidosis 1 70 0.049
99
CNG034 Congestive Heart Failure 69 0.049
100
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.049
101
P TRN020 Turner Syndrome 67 0.049
102
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.049
103
TTN003 Tetanus 65 0.049
104
GT001 Gout 64 0.049
105
P PRD008 Periodontitis 64 0.049
106
BLL006 Bullous Pemphigoid 62 0.049
107
P ART023 Arthropathy 62 0.049
108
c SCL052 Scleroderma, Familial Progressive 61 0.049
109
DCB001 Decubitus Ulcer 61 0.049
110
PNM010 Pneumothorax, Primary Spontaneous 60 0.049
111
LNG099 Lung Disease 60 0.049
112
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.049
113
P BND020 Bone Disease 59 0.049
114
c HPT016 Hepatitis B 59 0.049
115
GST045 Gastroenteritis 59 0.049
116
ADL030 Adult-Onset Still's Disease 58 0.049
117
PNM008 Pneumothorax 56 0.049
118
OCL020 Ocular Cicatricial Pemphigoid 55 0.049
119
c PRD040 Periodontitis, Chronic 53 0.049
120
P CTN003 Cutaneous Lupus Erythematosus 53 0.049
121
c VRL005 Viral Pneumonia 52 0.049
122
THR004 Thrombocytosis 51 0.049
123
PNN001 Panniculitis 51 0.049
124
MLL001 Molluscum Contagiosum 50 0.049
125
DYS073 Dysphagia 50 0.049
126
BNN003 Bone Inflammation Disease 48 0.049
127
SBC016 Subacute Delirium 44 0.049
128
NSP002 Nasopharyngitis 43 0.049
129
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.049
130
GST020 Gastric Antral Vascular Ectasia 41 0.049
131
PRM329 Premature Aging 35 0.049
132
PRN035 Perniosis 28 0.049
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