Search results for Isoniazid

456 hits were found for Isoniazid

# Family MCID Name MIFTS Score
1
ISN002 Isoniazide Allergy 7 3.902
2
ACT133 Acetylation, Slow 23 2.912
3
PLM001 Pulmonary Tuberculosis 69 0.916
4
P MYC084 Mycobacterium Tuberculosis 1 68 0.638
5
TBR011 Tuberculous Meningitis 48 0.379
6
P MNN013 Meningitis 66 0.377
7
MLT006 Multidrug-Resistant Tuberculosis 48 0.273
8
P NRP001 Neuropathy 56 0.247
9
IMM167 Immune Deficiency Disease 78 0.226
10
HMN044 Human Immunodeficiency Virus Type 1 71 0.226
11
P LPS004 Lupus Erythematosus 61 0.226
12
ACQ007 Acquired Immunodeficiency Syndrome 60 0.219
13
HNS001 Hansen's Disease 34 0.216
14
P LPR021 Leprosy 3 69 0.214
15
VSL002 Visual Epilepsy 59 0.214
16
P SZR006 Seizure Disorder 56 0.214
17
P HPT021 Hepatitis 67 0.202
18
MTB004 Metabolic Acidosis 50 0.194
19
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.186
20
ALL026 Allergic Hypersensitivity Disease 62 0.178
21
P PRP019 Peripheral Nervous System Disease 58 0.175
22
OCL069 Ocular Motor Apraxia 51 0.175
23
P PLL002 Pellagra 46 0.169
24
NRT004 Neuritis 52 0.160
25
CMR002 Coumarin Resistance 56 0.156
26
P EXN002 Exanthem 57 0.153
27
P LVR013 Liver Disease 68 0.143
28
c RHB024 Rhabdomyosarcoma 2 67 0.143
29
MLR002 Miliary Tuberculosis 49 0.135
30
P ENC018 Encephalopathy 61 0.132
31
LNG099 Lung Disease 60 0.128
32
SLC006 Silicosis 56 0.124
33
EXT033 Extrapulmonary Tuberculosis 46 0.124
34
P PNC044 Pancreatitis 61 0.119
35
48X005 48,xyyy 39 0.119
36
P MLT020 Multiple Sclerosis 72 0.115
37
STT001 Status Epilepticus 60 0.115
38
OCL051 Ocular Tuberculosis 31 0.115
39
CHL079 Children's Interstitial Lung Disease 26 0.115
40
c SYS001 Systemic Lupus Erythematosus 86 0.111
41
DFC004 Deficiency Anemia 70 0.111
42
P TRN020 Turner Syndrome 67 0.111
43
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.111
44
c VRL010 Viral Hepatitis 52 0.111
45
RDC006 Red Cell Aplasia 43 0.111
46
P BLD134 Bladder Cancer 79 0.106
47
P PNM007 Pneumonia 68 0.106
48
ALC007 Alcohol Dependence 66 0.106
49
c HPT003 Hepatitis a 62 0.106
50
c ACT027 Acute Pancreatitis 60 0.106
51
c ACT134 Acute Liver Failure 56 0.106
52
47X002 47,xyy 49 0.106
53
P PRR002 Pure Red-Cell Aplasia 47 0.106
54
P KDN018 Kidney Disease 72 0.101
55
P HNT016 Huntington Disease 72 0.101
56
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.101
57
P TRM003 Tremor 54 0.101
58
PYR009 Pyridoxine Deficiency Anemia 34 0.101
59
PYR016 Pyridoxine Deficiency 30 0.101
60
P HYP098 Hypereosinophilic Syndrome 67 0.096
61
DRM006 Dermatitis 61 0.096
62
END086 End Stage Renal Disease 51 0.096
63
LPR001 Lepromatous Leprosy 50 0.096
64
P SDR003 Sideroblastic Anemia 49 0.096
65
DRG002 Drug-Induced Hepatitis 43 0.096
66
CYT002 Cytokine Deficiency 42 0.096
67
MYC017 Mycobacterium Kansasii 36 0.096
68
P RHM011 Rheumatoid Arthritis 80 0.090
69
c NRF023 Neurofibromatosis, Type Ii 80 0.090
70
P SRC025 Sarcoidosis 1 70 0.090
71
P DBT009 Diabetes Mellitus 64 0.090
72
c HPT001 Hepatitis C 62 0.090
73
CHL068 Cholestasis 61 0.090
74
P OPT006 Optic Nerve Disease 60 0.090
75
P ALC033 Alcohol Use Disorder 58 0.090
76
P OPT009 Optic Neuritis 57 0.090
77
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.090
78
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.090
79
PLR008 Pleurisy 50 0.090
80
GYN001 Gynecomastia 49 0.090
81
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.090
82
INF021 Infant Gynecomastia 31 0.090
83
P THR014 Thrombocytopenia 67 0.084
84
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.084
85
PLR001 Pleural Tuberculosis 49 0.084
86
RNL012 Renal Tuberculosis 33 0.084
87
HYP056 Hypoglycemia 66 0.078
88
P PSR002 Psoriasis 62 0.078
89
LYM021 Lymphadenitis 57 0.078
90
PST011 Pustulosis of Palm and Sole 52 0.078
91
PLR007 Pleural Empyema 50 0.078
92
ACT055 Actinomycosis 47 0.078
93
GRN017 Granulocytopenia 44 0.078
94
URG001 Urogenital Tuberculosis 28 0.078
95
AST005 Asthma 76 0.071
96
P HYD006 Hydrocephalus 66 0.071
97
PRT036 Peritonitis 64 0.071
98
PNM001 Pneumocystosis 59 0.071
99
ERY003 Erythema Multiforme 58 0.071
100
P UVT001 Uveitis 57 0.071
101
BCT022 Bacterial Infectious Disease 56 0.071
102
PRC013 Pericarditis 54 0.071
103
P LCT001 Lactic Acidosis 51 0.071
104
ATX019 Ataxia with Vitamin E Deficiency 42 0.071
105
MYC015 Mycobacterium Fortuitum 32 0.071
106
TBR009 Tuberculous Empyema 24 0.071
107
P EPL164 Epilepsy 71 0.064
108
ADL002 Adult Syndrome 70 0.064
109
P ART022 Arthritis 69 0.064
110
SVR097 Severe Cutaneous Adverse Reaction 69 0.064
111
P OCL013 Oculodentodigital Dysplasia 69 0.064
112
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.064
113
LSH001 Leishmaniasis 63 0.064
114
P NTR004 Neutropenia 63 0.064
115
CLT003 Colitis 62 0.064
116
P ART023 Arthropathy 62 0.064
117
P VSC011 Vasculitis 62 0.064
118
P PRP029 Porphyria 62 0.064
119
NTR005 Nutritional Deficiency Disease 62 0.064
120
c PRT132 Protoporphyria, Erythropoietic, 1 61 0.064
121
c HPT016 Hepatitis B 59 0.064
122
CNT047 Contact Dermatitis 58 0.064
123
PNM008 Pneumothorax 56 0.064
124
P PLY019 Polyneuropathy 56 0.064
125
P SBS003 Substance Abuse 55 0.064
126
PRP030 Purpura 54 0.064
127
NRT001 Neurotic Disorder 53 0.064
128
CHR073 Choreatic Disease 52 0.064
129
HYP014 Hyperuricemia 52 0.064
130
MNN009 Meningoencephalitis 49 0.064
131
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.064
132
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.064
133
KWS001 Kwashiorkor 44 0.064
134
P KLZ004 Kala-Azar 1 41 0.064
135
LYM010 Lymph Node Tuberculosis 41 0.064
136
INT046 Intestinal Tuberculosis 41 0.064
137
TBR008 Tuberculous Peritonitis 35 0.064
138
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.064
139
ERY066 Erythema Multiforme Major 30 0.064
140
ACT228 Acute Radiation Syndrome 29 0.064
141
EXF003 Exfoliative Dermatitis 27 0.064
142
ACT162 Acute Sensory Ataxic Neuropathy 26 0.064
143
MLR004 Malaria 81 0.055
144
CRH001 Crohn's Disease 74 0.055
145
ULC004 Ulcerative Colitis 73 0.055
146
P CNR004 Cone-Rod Dystrophy 2 73 0.055
147
c HPT073 Hepatitis C Virus 72 0.055
148
RCK004 Rickets 68 0.055
149
P PRP003 Porphyria Cutanea Tarda 67 0.055
150
ANG054 Angina Pectoris 66 0.055
151
P PLM036 Pulmonary Fibrosis 65 0.055
152
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.055
153
PRT037 Pertussis 65 0.055
154
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.055
155
BRC012 Brucellosis 64 0.055
156
PRP083 Porphyria, Acute Intermittent 64 0.055
157
c ATM011 Autoimmune Hepatitis 63 0.055
158
ATM095 Autoimmune Disease 62 0.055
159
CTN007 Cutaneous Leishmaniasis 62 0.055
160
PSR001 Psoriatic Arthritis 61 0.055
161
HPT019 Hepatic Encephalopathy 60 0.055
162
c ACT071 Acute Kidney Failure 60 0.055
163
IRN002 Iron Metabolism Disease 57 0.055
164
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.055
165
P CRD246 Cardiovascular System Disease 57 0.055
166
BLR008 Bilirubin Metabolic Disorder 57 0.055
167
P PNM006 Pneumoconiosis 56 0.055
168
AGN016 Aging 56 0.055
169
P DRR001 Diarrhea 55 0.055
170
P ALP008 Alopecia 54 0.055
171
IRD001 Iridocyclitis 53 0.055
172
TXC002 Toxic Encephalopathy 53 0.055
173
OST011 Osteomalacia 52 0.055
174
c ACT078 Acute Porphyria 51 0.055
175
DYS073 Dysphagia 50 0.055
176
PPL021 Papilledema 49 0.055
177
DRG013 Drug-Induced Lupus Erythematosus 48 0.055
178
ANT018 Anthracosis 48 0.055
179
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.055
180
SYN036 Syncope 45 0.055
181
HPT004 Hepatic Coma 45 0.055
182
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.055
183
P PHT010 Photoparoxysmal Response 1 42 0.055
184
GST020 Gastric Antral Vascular Ectasia 41 0.055
185
49X006 49, Xxxxy Syndrome 41 0.055
186
RDN001 Reading Disorder 40 0.055
187
ANG049 Angioedema Induced by Ace Inhibitors 40 0.055
188
CNT007 Central Nervous System Tuberculosis 39 0.055
189
OPT010 Optic Papillitis 38 0.055
190
PHN011 Phenytoin Toxicity 33 0.055
191
c FML324 Familial Porphyria Cutanea Tarda 31 0.055
192
PRT094 Protoporphyria, Erythropoietic, X-Linked 31 0.055
193
LRY007 Laryngeal Tuberculosis 31 0.055
194
CYT018 Cytochrome P450 2d6 Variant 27 0.055
195
CRD217 Cardiac Tuberculosis 26 0.055
196
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.055
197
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.045
198
P RSP003 Respiratory Failure 74 0.045
199
P SCH015 Schizophrenia 74 0.045
200
c HYP836 Hypercholesterolemia, Familial, 1 73 0.045
201
c SPN225 Spondyloarthropathy 1 73 0.045
202
ANX010 Anxiety 73 0.045
203
c CHR684 Chronic Kidney Disease 70 0.045
204
P MLN008 Melanoma 69 0.045
205
P LYM118 Lymphoma 68 0.045
206
SKN019 Skin Melanoma 68 0.045
207
P DMN002 Dementia 66 0.045
208
GRG001 Greig Cephalopolysyndactyly Syndrome 66 0.045
209
KRT019 Keratitis, Hereditary 65 0.045
210
OST017 Osteomyelitis 64 0.045
211
P HML002 Hemolytic Anemia 63 0.045
212
P TRC086 Trichohepatoenteric Syndrome 1 62 0.045
213
LVR012 Liver Cirrhosis 62 0.045
214
MSL001 Measles 62 0.045
215
P NPH012 Nephrotic Syndrome 60 0.045
216
P CYS018 Cystitis 59 0.045
217
CYT008 Cytomegalovirus Infection 57 0.045
218
HYP266 Hypoxia 57 0.045
219
P ANG015 Angioedema 57 0.045
220
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.045
221
c ESS001 Essential Tremor 56 0.045
222
RSC001 Rosacea 54 0.045
223
P PMP001 Pemphigus 54 0.045
224
PRT038 Protein-Energy Malnutrition 54 0.045
225
ANL018 Analbuminemia 54 0.045
226
c PST005 Posterior Uveitis 54 0.045
227
SNS003 Sensory Peripheral Neuropathy 54 0.045
228
PNC001 Pancytopenia 54 0.045
229
P LCH002 Lichen Planus 53 0.045
230
HYP801 Hyperferritinemia with or Without Cataract 53 0.045
231
P CTN003 Cutaneous Lupus Erythematosus 53 0.045
232
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.045
233
PRP016 Paraplegia 52 0.045
234
LGN006 Legionnaire Disease 52 0.045
235
SPN051 Spondylitis 51 0.045
236
MYL001 Myelitis 51 0.045
237
OPT003 Opiate Dependence 50 0.045
238
URM002 Uremia 49 0.045
239
VCC001 Vaccinia 49 0.045
240
WTH001 Withdrawal Disorder 48 0.045
241
P LYM024 Lymphatic System Disease 48 0.045
242
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.045
243
OPD006 Opioid Addiction 48 0.045
244
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.045
245
CHR031 Chromoblastomycosis 47 0.045
246
CRD001 Cardiac Tamponade 47 0.045
247
NSS002 Neisseria Meningitidis Infection 47 0.045
248
MNN020 Meningococcal Infection 46 0.045
249
P MYC033 Myoclonus 46 0.045
250
OPD001 Opioid Abuse 46 0.045
251
ANR004 Anuria 46 0.045
252
c PCH010 Pachyonychia Congenita 3 44 0.045
253
SCT002 Scotoma 44 0.045
254
c SRC023 Sarcoidosis 2 43 0.045
255
TRP009 Triple X Syndrome 42 0.045
256
MRS001 Marasmus 42 0.045
257
DRG024 Drug Allergy 42 0.045
258
BCK006 Back Pain 42 0.045
259
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.045
260
c CHR682 Chronic Bilirubin Encephalopathy 39 0.045
261
ABD004 Abdominal Tuberculosis 38 0.045
262
c LPR022 Leprosy 2 37 0.045
263
c SBC035 Subacute Cutaneous Lupus Erythematosus 32 0.045
264
INF009 Inflammatory Spondylopathy 31 0.045
265
c ACQ016 Acquired Pure Red Cell Aplasia 27 0.045
266
JVN026 Jeavons Syndrome 24 0.045
267
ANT078 Antipyrine Metabolism 24 0.045
268
TXC008 Toxic Optic Neuropathy 23 0.045
269
c IDP048 Idiopathic Posterior Uveitis 14 0.045
270
TBR012 Tuberculous Uveitis 14 0.045
271
P HPT023 Hepatocellular Carcinoma 100 0.032
272
P LNG032 Lung Cancer 98 0.032
273
P PRS040 Prostate Cancer 97 0.032
274
CYS001 Cystic Fibrosis 81 0.032
275
P LNG064 Lung Cancer Susceptibility 3 78 0.032
276
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.032
277
GLB015 Glioblastoma Multiforme 75 0.032
278
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.032
279
MLT157 Multiple System Atrophy 1 70 0.032
280
DWN001 Down Syndrome 70 0.032
281
P MYP004 Myopathy 70 0.032
282
P ASP006 Aspergillosis 69 0.032
283
P SLP006 Sleep Apnea 69 0.032
284
P LKM002 Leukemia 68 0.032
285
P MYS003 Myasthenia Gravis 68 0.032
286
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.032
287
P CHR012 Chronic Granulomatous Disease 67 0.032
288
PSY004 Psychotic Disorder 67 0.032
289
P BLD062 Bile Duct Cancer 67 0.032
290
MYC006 Mycosis Fungoides 66 0.032
291
P SKN015 Skin Carcinoma 66 0.032
292
P CNJ013 Conjunctivitis 65 0.032
293
P DYS154 Dystonia 65 0.032
294
DMN031 Dementia, Lewy Body 65 0.032
295
P PRS038 Personality Disorder 65 0.032
296
CLN015 Colon Adenocarcinoma 65 0.032
297
P THY023 Thymoma 65 0.032
298
GT001 Gout 64 0.032
299
PLG002 Plague 63 0.032
300
TKY002 Takayasu Arteritis 62 0.032
301
P HYP750 Hypertriglyceridemia, Familial 62 0.032
302
HYP066 Hyperglycemia 61 0.032
303
FTT001 Fatty Liver Disease 61 0.032
304
P ENC004 Encephalitis 61 0.032
305
RCT015 Reactive Arthritis 61 0.032
306
P KDN017 Kidney Cancer 60 0.032
307
P TXP001 Toxoplasmosis 60 0.032
308
VRC005 Varicose Veins 60 0.032
309
INS001 Insulinoma 60 0.032
310
P CHR285 Chronic Myelomonocytic Leukemia 60 0.032
311
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.032
312
SPP011 Suppression of Tumorigenicity 12 59 0.032
313
P RBL001 Rubella 59 0.032
314
P MYC008 Myocarditis 59 0.032
315
PRT013 Portal Hypertension 59 0.032
316
P SYP003 Syphilis 58 0.032
317
GLB001 Gilbert Syndrome 58 0.032
318
CCC001 Coccidioidomycosis 58 0.032
319
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.032
320
EYD002 Eye Disease 58 0.032
321
P PTY003 Pityriasis Rubra Pilaris 58 0.032
322
P CND004 Candidiasis 58 0.032
323
P GLM007 Glomerulonephritis 57 0.032
324
c ANM036 Anemia, Sideroblastic, 1 57 0.032
325
P HDC001 Headache 57 0.032
326
DSS009 Disseminated Intravascular Coagulation 57 0.032
327
THR024 Thrombosis 57 0.032
328
TRN018 Transitional Cell Carcinoma 56 0.032
329
ORL005 Oral Candidiasis 56 0.032
330
c GRV008 Graves Disease 1 56 0.032
331
HST011 Histoplasmosis 55 0.032
332
HYP005 Hypokalemia 55 0.032
333
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.032
334
P STR020 Strabismus 55 0.032
335
HDR002 Hidradenitis Suppurativa 55 0.032
336
P HYP076 Hyperthyroidism 55 0.032
337
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.032
338
SYN007 Synovitis 54 0.032
339
HYP060 Hyperinsulinism 54 0.032
340
TRD006 Tardive Dyskinesia 54 0.032
341
BRN014 Bronchopneumonia 54 0.032
342
THR013 Thoracic Outlet Syndrome 54 0.032
343
P INF037 Inflammatory Bowel Disease 54 0.032
344
HMS001 Hemosiderosis 54 0.032
345
PRC002 Paracoccidioidomycosis 54 0.032
346
NNL006 Non-Alcoholic Steatohepatitis 54 0.032
347
PLM012 Pulmonary Sarcoidosis 53 0.032
348
KRT006 Keratoconjunctivitis 53 0.032
349
P MNC007 Monocytic Leukemia 53 0.032
350
FNG017 Fungal Infectious Disease 53 0.032
351
HYP063 Hypersplenism 53 0.032
352
c MCR113 Microvascular Complications of Diabetes 3 52 0.032
353
DMY004 Demyelinating Disease 52 0.032
354
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.032
355
P RCT021 Rectum Cancer 52 0.032
356
c THY107 Thymoma, Familial 52 0.032
357
PTH003 Pathologic Nystagmus 52 0.032
358
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.032
359
CLR109 Colorectal Adenocarcinoma 51 0.032
360
c PRM108 Primary Progressive Multiple Sclerosis 51 0.032
361
ESP002 Esophageal Varix 51 0.032
362
P AST007 Astrocytoma 51 0.032
363
P ESN008 Eosinophilic Pneumonia 50 0.032
364
c INF145 Infantile Liver Failure Syndrome 1 50 0.032
365
P TMP001 Temporal Lobe Epilepsy 50 0.032
366
BTY001 Butyrylcholinesterase Deficiency 50 0.032
367
ENT004 Enthesopathy 49 0.032
368
HDR003 Hidradenitis 49 0.032
369
MCR004 Macroglobulinemia 49 0.032
370
CHL004 Cholelithiasis 49 0.032
371
c BCT013 Bacterial Pneumonia 48 0.032
372
c ACT150 Acute Adrenal Insufficiency 48 0.032
373
CRY014 Cryptococcal Meningitis 48 0.032
374
VTM033 Vitamin K Deficiency Bleeding 48 0.032
375
SPL018 Splenomegaly 48 0.032
376
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.032
377
P KRT005 Keratoacanthoma 48 0.032
378
P TRT019 Torticollis 48 0.032
379
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.032
380
MCR018 Microcytic Anemia 47 0.032
381
PPL002 Papillary Carcinoma 47 0.032
382
c MCR120 Microvascular Complications of Diabetes 7 47 0.032
383
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.032
384
RYN005 Raynaud Phenomenon 47 0.032
385
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.032
386
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.032
387
P BNG032 Benign Mesothelioma 46 0.032
388
OBS004 Obstructive Hydrocephalus 46 0.032
389
P TRN034 Transverse Myelitis 45 0.032
390
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.032
391
NRS003 Neurosyphilis 45 0.032
392
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.032
393
P CMM008 Communicating Hydrocephalus 45 0.032
394
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.032
395
MLC004 Mulchandani-Bhoj-Conlin Syndrome 44 0.032
396
SBC016 Subacute Delirium 44 0.032
397
TBR006 Tuberculoid Leprosy 44 0.032
398
TNS014 Tenosynovitis 44 0.032
399
HPT082 Hepatic Adenomas, Familial 44 0.032
400
BCT021 Bacterial Sepsis 44 0.032
401
P SYR001 Syringomyelia 44 0.032
402
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.032
403
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.032
404
CRS001 Crescentic Glomerulonephritis 43 0.032
405
MYC013 Mycobacterium Abscessus 43 0.032
406
OPP002 Opportunistic Mycosis 43 0.032
407
DSC009 Discoid Lupus Erythematosus 42 0.032
408
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.032
409
P AVS003 Avascular Necrosis 42 0.032
410
CRV043 Cervical Dystonia 42 0.032
411
GLC096 Galactorrhea 42 0.032
412
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.032
413
MCH006 Mechanical Strabismus 42 0.032
414
LMB024 Limbic Encephalitis 41 0.032
415
c MCR130 Microvascular Complications of Diabetes 6 41 0.032
416
c MCR133 Microvascular Complications of Diabetes 4 41 0.032
417
PRS063 Paresthesia 41 0.032
418
P RRH023 Rare Hereditary Hemochromatosis 41 0.032
419
BBN001 Bubonic Plague 41 0.032
420
ASY002 Asymptomatic Neurosyphilis 41 0.032
421
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.032
422
CHL045 Choline Deficiency Disease 39 0.032
423
WLL004 Wallerian Degeneration 39 0.032
424
ADP007 Adie Pupil 39 0.032
425
MTR007 Motor Peripheral Neuropathy 39 0.032
426
HYP001 Hypochromic Microcytic Anemia 38 0.032
427
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.032
428
P SLP003 Salpingitis 38 0.032
429
NST002 Nestor-Guillermo Progeria Syndrome 38 0.032
430
ACT167 Acute Generalized Exanthematous Pustulosis 37 0.032
431
SYR010 Syringomyelia, Noncommunicating Isolated 37 0.032
432
PLC002 Plica Syndrome 36 0.032
433
EPD005 Epidural Abscess 35 0.032
434
CHR178 Chromosomal Triplication 35 0.032
435
ECH002 Echolalia 34 0.032
436
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.032
437
GRN009 Granulomatous Hepatitis 33 0.032
438
CYT004 Cytomegalic Inclusion Disease 31 0.032
439
BLN009 Balanoposthitis 31 0.032
440
GRN004 Granulomatous Amebic Encephalitis 30 0.032
441
SKL001 Skeletal Tuberculosis 30 0.032
442
MTG001 Metagonimiasis 29 0.032
443
OCC001 Occupational Dermatitis 29 0.032
444
SGM008 Segmental Dystonia 28 0.032
445
SPP001 Suppurative Lymphadenitis 27 0.032
446
HNM002 Hinman Syndrome 27 0.032
447
ACT038 Acute Retrobulbar Neuritis 27 0.032
448
MYC018 Mycobacterium Malmoense 26 0.032
449
TBR002 Tuberculous Salpingitis 26 0.032
450
AST054 Australia Antigen 26 0.032
451
DST016 Distomatosis 24 0.032
452
PHL001 Phlyctenulosis 21 0.032
453
PRN068 Paraneoplastic Limbic Encephalitis 21 0.032
454
c PLL014 Pellagra-Like Syndrome 18 0.032
455
HMR013 Hemorrhagic Proctocolitis 17 0.032
456
XLN067 X-Linked Protoporphyria 16 0.032
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