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Search results for Methimazole

295 hits were found for Methimazole

# Family MCID Name MIFTS Score
1
MTH070 Methimazole Antenatal Exposure 17 8.293
2
P HYP076 Hyperthyroidism 55 0.600
3
P GRV001 Graves' Disease 55 0.579
4
P HYP086 Hypothyroidism 69 0.363
5
GRN017 Granulocytopenia 44 0.315
6
c GRV008 Graves Disease 1 56 0.292
7
GTR002 Goiter 53 0.270
8
P THY032 Thyroiditis 52 0.194
9
P VSC011 Vasculitis 62 0.183
10
P NTR004 Neutropenia 63 0.180
11
ATM095 Autoimmune Disease 62 0.159
12
HRT040 Hirata Disease 38 0.159
13
P APL001 Aplastic Anemia 74 0.145
15
CHN065 Choanal Atresia, Posterior 49 0.140
16
HYP344 Hyperthyroidism, Familial Gestational 39 0.140
17
CHL068 Cholestasis 61 0.135
18
HSH003 Hashimoto Thyroiditis 62 0.130
19
ESP020 Esophageal Atresia 62 0.124
20
P LPS004 Lupus Erythematosus 61 0.118
21
APL023 Aplasia Cutis Congenita, Nonsyndromic 45 0.118
22
DFC004 Deficiency Anemia 70 0.112
23
P HPT021 Hepatitis 67 0.112
24
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.112
25
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.112
26
P PNC044 Pancreatitis 61 0.112
27
c ACT027 Acute Pancreatitis 60 0.112
28
EXP004 Exophthalmos 52 0.112
29
PLM011 Plummer's Disease 35 0.112
30
HYP056 Hypoglycemia 66 0.106
31
ANC002 Anca-Associated Vasculitis 41 0.106
32
c SYS001 Systemic Lupus Erythematosus 86 0.099
33
P ART022 Arthritis 69 0.099
34
ALL026 Allergic Hypersensitivity Disease 62 0.099
35
THY030 Thyroid Gland Disease 52 0.099
36
NDL007 Nodular Goiter 47 0.099
37
P MLT008 Multinodular Goiter 42 0.099
38
P EXN002 Exanthem 57 0.092
39
P LPR021 Leprosy 3 69 0.084
40
P GLM007 Glomerulonephritis 57 0.084
41
49X006 49, Xxxxy Syndrome 41 0.084
42
48X005 48,xyyy 39 0.084
43
ATM052 Autoimmune Disease 1 37 0.084
44
HNS001 Hansen's Disease 34 0.084
45
P RHM011 Rheumatoid Arthritis 80 0.075
46
INS024 Insulin-Like Growth Factor I 79 0.075
47
PND002 Pendred Syndrome 65 0.075
48
c CNG006 Congenital Hypothyroidism 64 0.075
49
DPR016 Depression 63 0.075
50
EYD002 Eye Disease 58 0.075
51
c DWL002 Dowling-Degos Disease 1 58 0.075
52
P MYS005 Myositis 56 0.075
53
CLB010 Coloboma of Macula 52 0.075
54
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.075
55
c BRS108 Breasts and/or Nipples, Aplasia or Hypoplasia of, 1 22 0.075
56
LYM053 Lymphomatous Thyroiditis 22 0.075
57
RTN123 Retinochoroidal Coloboma 20 0.075
58
CRB177 Carbimazole Sensitivity 7 0.075
59
P MYP004 Myopathy 70 0.065
60
P MYS003 Myasthenia Gravis 68 0.065
61
P TRN020 Turner Syndrome 67 0.065
62
P HYP098 Hypereosinophilic Syndrome 67 0.065
63
P DRM010 Dermatomyositis 61 0.065
64
INS001 Insulinoma 60 0.065
65
INC002 Inclusion Body Myositis 58 0.065
66
DSS008 Disease of Mental Health 58 0.065
67
MNT002 Mental Depression 58 0.065
68
P PLY041 Polymyositis 57 0.065
69
P CRD246 Cardiovascular System Disease 57 0.065
70
PNC001 Pancytopenia 54 0.065
71
P MSC003 Muscular Atrophy 52 0.065
72
RTN020 Retinal Vascular Disease 46 0.065
73
MYX004 Myxedema 43 0.065
74
c SYS043 Systemic Lupus Erythematosus 1 38 0.065
75
P OVR096 Overlap Myositis 27 0.065
76
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.053
77
P GLM040 Glioma Susceptibility 1 81 0.053
78
GLB015 Glioblastoma Multiforme 75 0.053
79
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.053
80
P LYM118 Lymphoma 68 0.053
81
RCK004 Rickets 68 0.053
82
P THR014 Thrombocytopenia 67 0.053
83
P MSC005 Muscular Dystrophy 66 0.053
84
P ATR011 Atrial Fibrillation 66 0.053
85
MSC007 Muscle Hypertrophy 64 0.053
86
c ATM011 Autoimmune Hepatitis 63 0.053
87
CLT003 Colitis 62 0.053
88
P PSR002 Psoriasis 62 0.053
89
c HPT003 Hepatitis a 62 0.053
90
P HYP750 Hypertriglyceridemia, Familial 62 0.053
91
FTT001 Fatty Liver Disease 61 0.053
92
P SJG008 Sjogren Syndrome 61 0.053
93
P NPH012 Nephrotic Syndrome 60 0.053
94
P VNT002 Ventricular Septal Defect 60 0.053
95
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.053
96
P OPT006 Optic Nerve Disease 60 0.053
97
PRT013 Portal Hypertension 59 0.053
98
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.053
99
P URT039 Urticaria 58 0.053
100
BLR008 Bilirubin Metabolic Disorder 57 0.053
101
P NRP001 Neuropathy 56 0.053
102
HYP005 Hypokalemia 55 0.053
103
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 55 0.053
104
PRP030 Purpura 54 0.053
105
P INF037 Inflammatory Bowel Disease 54 0.053
106
PRC013 Pericarditis 54 0.053
107
P TRM003 Tremor 54 0.053
108
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.053
109
P CTN003 Cutaneous Lupus Erythematosus 53 0.053
110
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 53 0.053
111
c VRL010 Viral Hepatitis 52 0.053
112
NRT004 Neuritis 52 0.053
113
PST011 Pustulosis of Palm and Sole 52 0.053
114
OLG003 Oligohydramnios 51 0.053
115
P MMB011 Membranous Nephropathy 50 0.053
116
FSC004 Fasciitis 50 0.053
117
P OMP004 Omphalocele 50 0.053
118
HRT011 Heart Septal Defect 50 0.053
119
47X002 47,xyy 49 0.053
120
P PRR002 Pure Red-Cell Aplasia 47 0.053
121
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.053
122
KRT013 Keratolytic Winter Erythema 46 0.053
123
c PRM038 Primary Agammaglobulinemia 44 0.053
124
RDC006 Red Cell Aplasia 43 0.053
125
ORB013 Orbital Disease 42 0.053
126
END028 Endemic Goiter 37 0.053
127
ABD010 Abdominal Wall Defect 36 0.053
128
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.053
129
THY001 Thyroid Crisis 31 0.053
130
c HYP595 Hypertension, Essential 84 0.037
131
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.037
132
AST005 Asthma 76 0.037
133
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.037
134
P HRT032 Heart Disease 75 0.037
135
P RSP003 Respiratory Failure 74 0.037
136
CRH001 Crohn's Disease 74 0.037
137
c SPN225 Spondyloarthropathy 1 73 0.037
138
ANX010 Anxiety 73 0.037
139
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.037
140
P NRB001 Neuroblastoma 72 0.037
141
HMN044 Human Immunodeficiency Virus Type 1 71 0.037
142
c EXD008 Exudative Vitreoretinopathy 1 71 0.037
143
CNG034 Congestive Heart Failure 69 0.037
144
P ASP006 Aspergillosis 69 0.037
145
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.037
146
SVR097 Severe Cutaneous Adverse Reaction 69 0.037
147
LYM133 Lymphoma, Hodgkin, Classic 69 0.037
148
P ANG001 Angelman Syndrome 69 0.037
149
P LVR013 Liver Disease 68 0.037
150
ALL003 Allergic Rhinitis 67 0.037
151
ALC007 Alcohol Dependence 66 0.037
152
P CNJ013 Conjunctivitis 65 0.037
153
BRR014 Barrett Esophagus 65 0.037
154
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.037
155
OST017 Osteomyelitis 64 0.037
156
P HML002 Hemolytic Anemia 63 0.037
157
P RNL100 Renal Hypodysplasia/aplasia 1 63 0.037
158
P ANR048 Aniridia 1 63 0.037
159
SKN016 Skin Disease 63 0.037
160
P SHR029 Short Syndrome 63 0.037
161
ANR007 Anorexia Nervosa 63 0.037
162
c FNC043 Fanconi Anemia, Complementation Group E 62 0.037
163
c BRN108 Branchiootic Syndrome 1 62 0.037
164
P ESP024 Esophagitis 62 0.037
165
P TRC086 Trichohepatoenteric Syndrome 1 62 0.037
166
P ART023 Arthropathy 62 0.037
167
P PRM006 Primary Biliary Cirrhosis 62 0.037
168
LVR012 Liver Cirrhosis 62 0.037
169
NTR005 Nutritional Deficiency Disease 62 0.037
170
HYP066 Hyperglycemia 61 0.037
171
P ENC018 Encephalopathy 61 0.037
172
HPT019 Hepatic Encephalopathy 60 0.037
173
ACN002 Acanthosis Nigricans 60 0.037
174
LNG099 Lung Disease 60 0.037
175
c ACT071 Acute Kidney Failure 60 0.037
176
P MYC008 Myocarditis 59 0.037
177
c HPT016 Hepatitis B 59 0.037
178
THY029 Thyroid Carcinoma 59 0.037
179
P GLL022 Guillain-Barre Syndrome 59 0.037
180
ISC004 Ischemia 58 0.037
181
P ALC033 Alcohol Use Disorder 58 0.037
182
ERY003 Erythema Multiforme 58 0.037
183
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.037
184
P UVT001 Uveitis 57 0.037
185
P OPT009 Optic Neuritis 57 0.037
186
P RHN004 Rhinitis 57 0.037
187
P FCL005 Focal Segmental Glomerulosclerosis 57 0.037
188
TNS005 Tonsillitis 57 0.037
189
HYP266 Hypoxia 57 0.037
190
PHR003 Pharyngitis 57 0.037
191
GST050 Gastrointestinal System Disease 56 0.037
192
MCR141 Mucormycosis 56 0.037
193
P GST044 Gastritis 56 0.037
194
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.037
195
MMB001 Membranoproliferative Glomerulonephritis 55 0.037
196
P DRR001 Diarrhea 55 0.037
197
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.037
198
SYN007 Synovitis 54 0.037
199
HYP060 Hyperinsulinism 54 0.037
200
P ALP008 Alopecia 54 0.037
201
THR013 Thoracic Outlet Syndrome 54 0.037
202
PTT009 Pituitary Gland Disease 54 0.037
203
CLL003 Cellulitis 54 0.037
204
GST009 Gastroschisis 53 0.037
205
CRH005 Crohn's Colitis 53 0.037
206
HMC014 Homocysteinemia 53 0.037
207
GST023 Gastric Ulcer 53 0.037
208
P PNC025 Panic Disorder 53 0.037
209
c GLL024 Gallbladder Disease 1 53 0.037
210
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.037
211
P HYP730 Hypogonadotropic Hypogonadism 52 0.037
212
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.037
213
THR004 Thrombocytosis 51 0.037
214
OCL069 Ocular Motor Apraxia 51 0.037
215
ILS001 Ileus 51 0.037
216
PNN001 Panniculitis 51 0.037
217
P CHL066 Cholangitis 51 0.037
218
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.037
219
HYP081 Hypolipoproteinemia 51 0.037
220
DYS073 Dysphagia 50 0.037
221
LPR001 Lepromatous Leprosy 50 0.037
222
HYP080 Hypogonadism 50 0.037
223
GYN001 Gynecomastia 49 0.037
224
P SDR003 Sideroblastic Anemia 49 0.037
225
BNR002 Bone Resorption Disease 48 0.037
226
NCR007 Necrotizing Fasciitis 48 0.037
227
P SCL009 Sclerosing Cholangitis 48 0.037
228
SPL018 Splenomegaly 48 0.037
229
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.037
230
c MLG069 Malignant Hypertension 47 0.037
231
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.037
232
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.037
233
P RTN014 Retinal Artery Occlusion 47 0.037
234
RYN005 Raynaud Phenomenon 47 0.037
235
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.037
236
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.037
237
FLL008 Folliculitis 46 0.037
238
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.037
239
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.037
240
HPT004 Hepatic Coma 45 0.037
241
TWN001 Twin-to-Twin Transfusion Syndrome 45 0.037
242
SYN005 Synostosis 45 0.037
243
MLN073 Melanosis, Neurocutaneous 45 0.037
244
c ATM099 Autoimmune Uveitis 45 0.037
245
CNT046 Central Nervous System Vasculitis 44 0.037
246
P CHR345 Chronic Pain 44 0.037
247
PTT037 Pituitary Tumors 44 0.037
248
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.037
249
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.037
250
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.037
251
CRS001 Crescentic Glomerulonephritis 43 0.037
252
c CNT028 Central Retinal Artery Occlusion 43 0.037
253
MCR103 Microtia 43 0.037
254
CYT002 Cytokine Deficiency 42 0.037
255
P PRT026 Parotitis 42 0.037
256
GTR011 Goiter, Multinodular 1, with or Without Sertoli-Leydig Cell Tumors 42 0.037
257
P BLL007 Bullous Skin Disease 41 0.037
258
BRN026 Branch Retinal Artery Occlusion 40 0.037
259
PPL035 Papillary Thyroid Microcarcinoma 39 0.037
260
c CHR682 Chronic Bilirubin Encephalopathy 39 0.037
261
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.037
262
MCK029 Meckel Diverticulum 38 0.037
263
SPL006 Splenic Infarction 38 0.037
264
PTT002 Potter's Syndrome 38 0.037
265
ACT167 Acute Generalized Exanthematous Pustulosis 37 0.037
266
HYP026 Hypoglycemic Coma 36 0.037
267
HRW001 Hair Whorl 36 0.037
268
PLC002 Plica Syndrome 36 0.037
269
ASC009 Ascites, Chylous 35 0.037
270
c ATM022 Autoimmune Myocarditis 35 0.037
271
c NNS007 Nonsyndromic Deafness 35 0.037
272
ATX010 Ataxia Neuropathy Spectrum 34 0.037
273
ACT064 Acute Necrotizing Encephalitis 33 0.037
274
NNT003 Neonatal Thyrotoxicosis 33 0.037
275
GRN009 Granulomatous Hepatitis 33 0.037
276
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.037
277
INF021 Infant Gynecomastia 31 0.037
278
ERY066 Erythema Multiforme Major 30 0.037
279
PCM002 Pauci-Immune Glomerulonephritis 30 0.037
280
MYC088 Mycobacterium Avium Complex Infections 29 0.037
281
c PSR024 Psoriasis 3 28 0.037
282
HYP855 Hyperpigmentation of the Skin 27 0.037
283
P CRY006 Cryofibrinogenemia 27 0.037
284
ECT089 Ectodermal Dysplasia, Hypohidrotic, with Hypothyroidism and Ciliary Dyskinesia 27 0.037
285
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.037
286
VSC052 Vasculitis, Lymphocytic, Nodular 25 0.037
287
ESN022 Eosinophilic Colitis 25 0.037
288
URT049 Urate Oxidase, Pseudogene 25 0.037
289
c DMN005 Diamond-Blackfan Anemia 2 25 0.037
290
c CHR686 Chronic Cutaneous Lupus Erythematosus 19 0.037
291
AND005 Androgen Insensitivity Syndrome, Mild 19 0.037
292
DRG017 Drug-Induced Vasculitis 17 0.037
293
BLD137 Blood Group--Ahonen 16 0.037
294
c GRV009 Graves Disease 2 15 0.037
295
BMF002 Bamforth Syndrome 13 0.037
The MalaCards human disease database index: 1-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
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