Search results for Pyrazinamide

151 hits were found for Pyrazinamide

# Family MCID Name MIFTS Score
1
PLM001 Pulmonary Tuberculosis 70 0.702
2
P MYC084 Mycobacterium Tuberculosis 1 68 0.494
3
MLT006 Multidrug-Resistant Tuberculosis 47 0.378
4
HYP014 Hyperuricemia 51 0.225
5
HMN044 Human Immunodeficiency Virus Type 1 71 0.204
6
ALL026 Allergic Hypersensitivity Disease 64 0.193
7
ACQ007 Acquired Immunodeficiency Syndrome 60 0.193
8
CMR002 Coumarin Resistance 56 0.193
9
IMM167 Immune Deficiency Disease 78 0.182
10
P MNN013 Meningitis 65 0.175
11
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.175
12
TBR011 Tuberculous Meningitis 48 0.175
13
GT001 Gout 63 0.169
14
ADL002 Adult Syndrome 69 0.141
15
P THR014 Thrombocytopenia 68 0.133
16
c RHB024 Rhabdomyosarcoma 2 65 0.133
17
DFC004 Deficiency Anemia 75 0.124
18
LNG099 Lung Disease 61 0.124
19
P HPT021 Hepatitis 67 0.115
20
P LPR021 Leprosy 3 67 0.115
21
P EXN002 Exanthem 57 0.115
22
BCT022 Bacterial Infectious Disease 56 0.115
23
47X002 47,xyy 49 0.115
24
DRG002 Drug-Induced Hepatitis 42 0.115
25
48X005 48,xyyy 39 0.115
26
HNS001 Hansen's Disease 34 0.115
27
MYC017 Mycobacterium Kansasii 37 0.105
28
P KDN018 Kidney Disease 70 0.094
29
P ART022 Arthritis 70 0.094
30
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.094
31
P TRN020 Turner Syndrome 65 0.094
32
SLC006 Silicosis 56 0.094
33
P HYP761 Hypouricemia, Renal, 1 42 0.094
34
c HPT003 Hepatitis a 63 0.081
35
NTR005 Nutritional Deficiency Disease 61 0.081
36
VRL011 Viral Infectious Disease 61 0.081
37
CHL068 Cholestasis 60 0.081
38
P SDR003 Sideroblastic Anemia 49 0.081
39
PPL021 Papilledema 48 0.081
40
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.081
41
TRP009 Triple X Syndrome 42 0.081
42
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.081
43
P XNT004 Xanthinuria 41 0.081
44
OPT010 Optic Papillitis 39 0.081
45
c HRD142 Hereditary Xanthinuria 32 0.081
46
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.066
47
P RHM011 Rheumatoid Arthritis 80 0.066
48
P CNR004 Cone-Rod Dystrophy 2 71 0.066
49
DWN001 Down Syndrome 70 0.066
50
P LVR013 Liver Disease 68 0.066
51
P PNM007 Pneumonia 68 0.066
52
GRG001 Greig Cephalopolysyndactyly Syndrome 67 0.066
53
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.066
54
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.066
55
LSH001 Leishmaniasis 63 0.066
56
P NTR004 Neutropenia 63 0.066
57
c ACT068 Acute Cystitis 63 0.066
58
CTN007 Cutaneous Leishmaniasis 61 0.066
59
BRC012 Brucellosis 61 0.066
60
GST045 Gastroenteritis 59 0.066
61
P URT039 Urticaria 58 0.066
62
BLR008 Bilirubin Metabolic Disorder 57 0.066
63
P UVT001 Uveitis 57 0.066
64
P DRR001 Diarrhea 57 0.066
65
PRS047 Prostatitis 56 0.066
66
P NRP001 Neuropathy 56 0.066
67
AGN016 Aging 56 0.066
68
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.066
69
ANL018 Analbuminemia 54 0.066
70
c PST005 Posterior Uveitis 54 0.066
71
c VRL010 Viral Hepatitis 51 0.066
72
c ACT134 Acute Liver Failure 51 0.066
73
LGN006 Legionnaire Disease 50 0.066
74
IRD001 Iridocyclitis 50 0.066
75
P LYM024 Lymphatic System Disease 48 0.066
76
CYT002 Cytokine Deficiency 44 0.066
77
P KLZ004 Kala-Azar 1 41 0.066
78
c LPR022 Leprosy 2 37 0.066
79
RNL012 Renal Tuberculosis 32 0.066
80
ACT162 Acute Sensory Ataxic Neuropathy 26 0.066
81
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.066
82
JVN026 Jeavons Syndrome 24 0.066
83
c IDP048 Idiopathic Posterior Uveitis 14 0.066
84
P LNG032 Lung Cancer 97 0.047
85
CYS001 Cystic Fibrosis 80 0.047
86
c HYP836 Hypercholesterolemia, Familial, 1 72 0.047
87
MLT157 Multiple System Atrophy 1 70 0.047
88
P AMY004 Amyloidosis 70 0.047
89
ABT001 Abetalipoproteinemia 67 0.047
90
P LKM002 Leukemia 66 0.047
91
P HYP098 Hypereosinophilic Syndrome 66 0.047
92
c SML038 Small Cell Cancer of the Lung 65 0.047
93
MYL031 Myeloproliferative Neoplasm 65 0.047
94
PRT036 Peritonitis 65 0.047
95
P MYP004 Myopathy 64 0.047
96
OST017 Osteomyelitis 64 0.047
97
c HPT001 Hepatitis C 63 0.047
98
LPD008 Lipid Metabolism Disorder 62 0.047
99
P VSC011 Vasculitis 62 0.047
100
PSR001 Psoriatic Arthritis 62 0.047
101
c ATM011 Autoimmune Hepatitis 62 0.047
102
DRM006 Dermatitis 61 0.047
103
P LPS004 Lupus Erythematosus 61 0.047
104
P MYC008 Myocarditis 59 0.047
105
P CHR285 Chronic Myelomonocytic Leukemia 59 0.047
106
END030 End Stage Renal Failure 58 0.047
107
ERY003 Erythema Multiforme 57 0.047
108
P HDC001 Headache 57 0.047
109
P PRP019 Peripheral Nervous System Disease 57 0.047
110
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.047
111
CYT008 Cytomegalovirus Infection 56 0.047
112
THR024 Thrombosis 56 0.047
113
HYP266 Hypoxia 56 0.047
114
DFF005 Diffuse Large B-Cell Lymphoma 56 0.047
115
P GST044 Gastritis 55 0.047
116
PRP030 Purpura 55 0.047
117
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.047
118
P MGL001 Megaloblastic Anemia 55 0.047
119
P THY032 Thyroiditis 53 0.047
120
OCL069 Ocular Motor Apraxia 51 0.047
121
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.047
122
ASP003 Aseptic Meningitis 51 0.047
123
HYP081 Hypolipoproteinemia 50 0.047
124
P FNC004 Fanconi Syndrome 50 0.047
125
c INF145 Infantile Liver Failure Syndrome 1 50 0.047
126
P DDN001 Duodenal Ulcer 50 0.047
127
c XNT010 Xanthinuria, Type I 50 0.047
128
LPR001 Lepromatous Leprosy 50 0.047
129
PLR001 Pleural Tuberculosis 50 0.047
130
PLR007 Pleural Empyema 49 0.047
131
MLR002 Miliary Tuberculosis 49 0.047
132
RFR010 Refractory Anemia 48 0.047
133
ATX019 Ataxia with Vitamin E Deficiency 48 0.047
134
INT067 Interstitial Nephritis 46 0.047
135
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 0.047
136
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 46 0.047
137
EXT033 Extrapulmonary Tuberculosis 46 0.047
138
P PLL002 Pellagra 45 0.047
139
P AVS003 Avascular Necrosis 42 0.047
140
ANG049 Angioedema Induced by Ace Inhibitors 40 0.047
141
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.047
142
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.047
143
TBR008 Tuberculous Peritonitis 36 0.047
144
GRN009 Granulomatous Hepatitis 31 0.047
145
CYT004 Cytomegalic Inclusion Disease 31 0.047
146
EXF003 Exfoliative Dermatitis 27 0.047
147
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.047
148
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.047
149
CHL079 Children's Interstitial Lung Disease 27 0.047
150
AST054 Australia Antigen 26 0.047
151
TBR009 Tuberculous Empyema 24 0.047
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