Search results for methanol

496 hits were found for methanol

# Family MCID Name MIFTS Score
1
MTH047 Methanol Poisoning 30 4.234
2
MTB004 Metabolic Acidosis 50 0.381
3
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.257
4
OCL069 Ocular Motor Apraxia 52 0.204
5
P OPT006 Optic Nerve Disease 58 0.190
6
P DRR001 Diarrhea 56 0.185
7
GST023 Gastric Ulcer 53 0.171
8
P NRP001 Neuropathy 57 0.163
9
RPD005 Rapidly Involuting Congenital Hemangioma 39 0.157
10
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.157
11
ETH012 Ethylene Glycol Poisoning 22 0.157
12
RHM027 Rheumatic Disease 56 0.151
13
ENT004 Enthesopathy 49 0.151
14
HYP066 Hyperglycemia 61 0.144
15
P GST044 Gastritis 56 0.141
16
HRW001 Hair Whorl 36 0.141
17
DYS015 Dysentery 50 0.138
18
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 66 0.134
19
P ALC033 Alcohol Use Disorder 59 0.127
20
BCT022 Bacterial Infectious Disease 56 0.123
21
HLX001 Helix Syndrome 48 0.123
22
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.119
23
P HPT023 Hepatocellular Carcinoma 100 0.115
24
BRN024 Bronchitis 69 0.115
25
ALC007 Alcohol Dependence 67 0.111
26
47X002 47,xyy 49 0.111
27
c DNT047 Dentinogenesis Imperfecta Type 2 33 0.107
28
TXC008 Toxic Optic Neuropathy 23 0.107
29
SKN016 Skin Disease 63 0.102
30
MTH071 Methane Production 26 0.102
31
QFV001 Q Fever 58 0.097
32
48X005 48,xyyy 39 0.097
33
PRT036 Peritonitis 65 0.092
34
CLF027 Cleft Palate, Isolated 65 0.092
35
c PCH010 Pachyonychia Congenita 3 44 0.092
36
P LVR013 Liver Disease 68 0.087
37
ALL026 Allergic Hypersensitivity Disease 64 0.087
38
ORL011 Oral Cancer 60 0.087
39
NRT004 Neuritis 54 0.087
40
EXN003 Exencephaly 31 0.087
41
P CLR023 Colorectal Cancer 99 0.081
42
P BRS047 Breast Cancer 97 0.081
43
LPD008 Lipid Metabolism Disorder 63 0.081
44
P OPT009 Optic Neuritis 57 0.081
45
c PLM127 Pulmonary Hypertension, Primary, 3 33 0.081
46
P SKN015 Skin Carcinoma 67 0.075
47
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.075
48
DRM006 Dermatitis 62 0.075
49
AMN003 Amnestic Disorder 55 0.075
50
P TRM003 Tremor 54 0.075
51
WTH001 Withdrawal Disorder 49 0.075
52
KLB003 Klebsiella Pneumonia 39 0.075
53
GLB015 Glioblastoma Multiforme 75 0.069
54
P RSP003 Respiratory Failure 75 0.069
55
HYP056 Hypoglycemia 66 0.069
56
GT001 Gout 64 0.069
57
P CTR002 Cataract 61 0.069
58
P BRS044 Breast Adenocarcinoma 59 0.069
59
PPT005 Peptic Ulcer Disease 59 0.069
60
P BCL017 B-Cell Lymphoma 58 0.069
61
CNT047 Contact Dermatitis 58 0.069
62
SCH014 Schistosomiasis 57 0.069
63
P FBR017 Fibrosarcoma 57 0.069
64
P LCT001 Lactic Acidosis 51 0.069
65
BNR002 Bone Resorption Disease 49 0.069
66
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.069
67
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.069
68
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 25 0.069
69
P LNG032 Lung Cancer 98 0.062
70
MLR004 Malaria 81 0.062
71
CRV035 Cervical Cancer 76 0.062
72
P OST002 Osteoporosis 74 0.062
73
c HYP836 Hypercholesterolemia, Familial, 1 73 0.062
74
KRT019 Keratitis, Hereditary 68 0.062
75
P DYS154 Dystonia 65 0.062
76
P ADN016 Adenocarcinoma 64 0.062
77
CLN015 Colon Adenocarcinoma 64 0.062
78
LSH001 Leishmaniasis 64 0.062
79
CLT003 Colitis 63 0.062
80
P PSR002 Psoriasis 63 0.062
81
ISC004 Ischemia 61 0.062
82
P SZR006 Seizure Disorder 59 0.062
83
P HDC001 Headache 58 0.062
84
VSL002 Visual Epilepsy 57 0.062
85
CMM005 Common Cold 56 0.062
86
P PLY019 Polyneuropathy 56 0.062
87
PST011 Pustulosis of Palm and Sole 53 0.062
88
PLR008 Pleurisy 51 0.062
89
P HMR005 Hemorrhoid 46 0.062
90
P KLZ004 Kala-Azar 1 42 0.062
91
MRP001 Morphine Dependence 41 0.062
92
MLC004 Mulchandani-Bhoj-Conlin Syndrome 33 0.062
93
NRL016 Neural Tube Defects 83 0.053
94
BRN028 Brain Cancer 74 0.053
95
ULC004 Ulcerative Colitis 73 0.053
96
ANX010 Anxiety 73 0.053
97
P NRB001 Neuroblastoma 72 0.053
98
P KDN018 Kidney Disease 71 0.053
99
SKN019 Skin Melanoma 68 0.053
100
P HYP098 Hypereosinophilic Syndrome 66 0.053
101
c SML038 Small Cell Cancer of the Lung 66 0.053
102
DPR016 Depression 64 0.053
103
MSL001 Measles 61 0.053
104
ATM095 Autoimmune Disease 61 0.053
105
P TXP001 Toxoplasmosis 61 0.053
106
c ACT027 Acute Pancreatitis 60 0.053
107
P URT039 Urticaria 58 0.053
108
CNS004 Constipation 58 0.053
109
P INF032 Infertility 58 0.053
110
P RHN004 Rhinitis 58 0.053
111
P PRP019 Peripheral Nervous System Disease 58 0.053
112
MNT002 Mental Depression 57 0.053
113
HYP005 Hypokalemia 56 0.053
114
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 56 0.053
115
ECH003 Echinococcosis 53 0.053
116
SPP010 Suppressor of Tumorigenicity 3 51 0.053
117
NNL006 Non-Alcoholic Steatohepatitis 51 0.053
118
SCB001 Scabies 51 0.053
119
GSG001 Gas Gangrene 51 0.053
120
PRS034 Parasitic Helminthiasis Infectious Disease 50 0.053
121
ASP007 Aspiration Pneumonia 48 0.053
122
SXL003 Sexual Disorder 48 0.053
123
NWC001 Newcastle Disease 45 0.053
124
CRB004 Cerebral Artery Occlusion 45 0.053
125
SBC016 Subacute Delirium 44 0.053
126
CYT002 Cytokine Deficiency 44 0.053
127
CHD004 Chudley-Mccullough Syndrome 44 0.053
128
TST015 Testicular Disease 44 0.053
129
ORL015 Oral Squamous Cell Carcinoma 43 0.053
130
STC004 Stachybotrys Chartarum 34 0.053
131
c PLM128 Pulmonary Hypertension, Primary, 2 29 0.053
132
PST092 Posttransplant Acute Limbic Encephalitis 29 0.053
133
OST151 Osteoporosis and Oculocutaneous Hypopigmentation Syndrome 24 0.053
134
OBS532 Obsolete: Ehlers-Danlos Syndrome, Fibronectinemic Type 15 0.053
135
P PRS040 Prostate Cancer 98 0.044
136
c AMY091 Amyotrophic Lateral Sclerosis 1 90 0.044
137
P GST053 Gastric Cancer 84 0.044
138
c LKM061 Leukemia, Acute Myeloid 83 0.044
139
P RHM011 Rheumatoid Arthritis 81 0.044
140
P BLD134 Bladder Cancer 79 0.044
141
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.044
142
P PHC003 Pheochromocytoma 72 0.044
143
GST040 Gastric Adenocarcinoma 71 0.044
144
c MGR028 Migraine with or Without Aura 1 70 0.044
145
P INF038 Influenza 68 0.044
146
ALL003 Allergic Rhinitis 68 0.044
147
CRP001 Carpal Tunnel Syndrome 67 0.044
148
OST159 Osteogenic Sarcoma 67 0.044
149
ATH013 Atherosclerosis Susceptibility 66 0.044
150
P NRV007 Nervous System Disease 66 0.044
151
P HRP006 Herpes Simplex 65 0.044
152
P DBT009 Diabetes Mellitus 65 0.044
153
P MTR014 Motor Neuron Disease 65 0.044
154
LVR012 Liver Cirrhosis 64 0.044
155
TYP007 Typhoid Fever 63 0.044
156
P NTR004 Neutropenia 63 0.044
157
CTN007 Cutaneous Leishmaniasis 62 0.044
158
TXC005 Toxic Shock Syndrome 62 0.044
159
P ENC004 Encephalitis 62 0.044
160
P ENC018 Encephalopathy 61 0.044
161
P PNC044 Pancreatitis 61 0.044
162
PND002 Pendred Syndrome 61 0.044
163
MCR013 Microphthalmia 61 0.044
164
APP008 Appendicitis 60 0.044
165
CHC001 Chickenpox 60 0.044
166
P SLP005 Sleep Disorder 60 0.044
167
c ACT071 Acute Kidney Failure 60 0.044
168
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.044
169
c DNG003 Dengue Disease 60 0.044
170
GST045 Gastroenteritis 60 0.044
171
RBS001 Rabies 58 0.044
172
IRN002 Iron Metabolism Disease 58 0.044
173
TNS005 Tonsillitis 57 0.044
174
PLM031 Poliomyelitis 57 0.044
175
VSC002 Vascular Dementia 57 0.044
176
HYP266 Hypoxia 57 0.044
177
PRS047 Prostatitis 57 0.044
178
c ACT075 Acute Myocardial Infarction 57 0.044
179
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.044
180
P MLN007 Male Infertility 56 0.044
181
P INF037 Inflammatory Bowel Disease 56 0.044
182
GST050 Gastrointestinal System Disease 56 0.044
183
CHL014 Cholera 56 0.044
184
SHG001 Shigellosis 56 0.044
185
VSC003 Visceral Leishmaniasis 55 0.044
186
DBT010 Diabetic Neuropathy 55 0.044
187
FRY006 Fryns Microphthalmia Syndrome 55 0.044
188
P LTR001 Lateral Sclerosis 54 0.044
189
CHR100 Chronic Ulcer of Skin 54 0.044
190
CCC001 Coccidioidomycosis 54 0.044
191
ALC009 Alcoholic Liver Cirrhosis 54 0.044
192
PRS045 Prostatic Hypertrophy 52 0.044
193
P LRY019 Laryngitis 52 0.044
194
PRS021 Prostatic Adenoma 51 0.044
195
PTH003 Pathologic Nystagmus 51 0.044
196
CLR109 Colorectal Adenocarcinoma 51 0.044
197
STM007 Stomatitis 51 0.044
198
P SCK005 Sickle Cell Disease 51 0.044
199
P DDN001 Duodenal Ulcer 50 0.044
200
P AST007 Astrocytoma 50 0.044
201
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 50 0.044
202
BRN071 Brain Injury 50 0.044
203
PRS129 Prostatic Hyperplasia, Benign 49 0.044
204
MCP006 Mucoepidermoid Carcinoma 49 0.044
205
SLP001 Sleeping Sickness 49 0.044
206
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.044
207
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.044
208
P CRV031 Cervical Adenocarcinoma 47 0.044
209
RFT001 Rift Valley Fever 47 0.044
210
RTN023 Retinitis 47 0.044
211
ADR040 Adrenal Gland Pheochromocytoma 46 0.044
212
CYN002 Cyanosis, Transient Neonatal 46 0.044
213
P MYG005 Myoglobinuria 44 0.044
214
NRR001 Neuroretinitis 43 0.044
215
ART006 Arthus Reaction 43 0.044
216
BCK006 Back Pain 42 0.044
217
ANX004 Anoxia 42 0.044
218
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.044
219
ORM002 Oromandibular Dystonia 39 0.044
220
ACN019 Acanthamoeba Keratitis 31 0.044
221
CRV071 Cervical Rib 24 0.044
222
CRN311 Coronary Ostial Stenosis or Atresia 20 0.044
223
ANT040 Anton's Syndrome 16 0.044
224
ESP021 Esophageal Cancer 91 0.031
225
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.031
226
P ALZ034 Alzheimer Disease 89 0.031
227
c SYS001 Systemic Lupus Erythematosus 87 0.031
228
P ATX030 Ataxia-Telangiectasia 84 0.031
229
STR067 Stroke, Ischemic 80 0.031
230
CYS001 Cystic Fibrosis 80 0.031
231
INS024 Insulin-Like Growth Factor I 80 0.031
232
P LNG064 Lung Cancer Susceptibility 3 78 0.031
233
P RTN008 Retinitis Pigmentosa 78 0.031
234
P PRK057 Parkinson Disease, Late-Onset 77 0.031
235
P NRF023 Neurofibromatosis, Type Ii 77 0.031
236
P HRT032 Heart Disease 76 0.031
237
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.031
238
DFC004 Deficiency Anemia 75 0.031
239
SVR004 Severe Combined Immunodeficiency 74 0.031
240
c SPN225 Spondyloarthropathy 1 74 0.031
241
SCK003 Sickle Cell Anemia 73 0.031
242
P MLT020 Multiple Sclerosis 72 0.031
243
HMN044 Human Immunodeficiency Virus Type 1 71 0.031
244
P MYC007 Myocardial Infarction 71 0.031
245
c HPT073 Hepatitis C Virus 71 0.031
246
P ART022 Arthritis 71 0.031
247
PLM001 Pulmonary Tuberculosis 70 0.031
248
CNG034 Congestive Heart Failure 70 0.031
249
CRB039 Cerebrovascular Disease 69 0.031
250
P HYP086 Hypothyroidism 69 0.031
251
P LKM062 Leukemia, Acute Lymphoblastic 69 0.031
252
P LYM118 Lymphoma 69 0.031
253
P HLP001 Holoprosencephaly 69 0.031
254
OBS002 Obsessive-Compulsive Disorder 69 0.031
255
LYM007 Lymphangioleiomyomatosis 69 0.031
256
P THR014 Thrombocytopenia 68 0.031
257
P PNM007 Pneumonia 68 0.031
258
P MJR001 Major Depressive Disorder 68 0.031
259
c ATS007 Autism Spectrum Disorder 68 0.031
260
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.031
261
P HPT021 Hepatitis 68 0.031
262
P ANG001 Angelman Syndrome 67 0.031
263
c NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 67 0.031
264
MLD001 Melioidosis 67 0.031
265
P LKM002 Leukemia 67 0.031
266
c CHR684 Chronic Kidney Disease 67 0.031
267
P DRM053 Dermatitis, Atopic 67 0.031
268
AND002 Androgen Insensitivity Syndrome 67 0.031
269
UND005 Undifferentiated Pleomorphic Sarcoma 67 0.031
270
LPT001 Leptospirosis 67 0.031
271
ART001 Arterial Tortuosity Syndrome 66 0.031
272
c PRD013 Periodic Fever, Familial, Autosomal Dominant 66 0.031
273
P CNJ013 Conjunctivitis 66 0.031
274
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.031
275
P ATS364 Autism 65 0.031
276
BRR014 Barrett Esophagus 65 0.031
277
TBC004 Tobacco Addiction 64 0.031
278
TTN003 Tetanus 64 0.031
279
IRR002 Irritable Bowel Syndrome 64 0.031
280
P VSC007 Vascular Disease 64 0.031
281
IDP011 Idiopathic Interstitial Pneumonia 64 0.031
282
MSC007 Muscle Hypertrophy 64 0.031
283
P CRN018 Coronary Artery Anomaly 64 0.031
284
P CRN300 Coronary Heart Disease 1 64 0.031
285
c HPT001 Hepatitis C 63 0.031
286
P GLM045 Glioma 63 0.031
287
c ACT068 Acute Cystitis 63 0.031
288
ANR007 Anorexia Nervosa 63 0.031
289
c HPT003 Hepatitis a 63 0.031
290
P ANR048 Aniridia 1 63 0.031
291
P HML002 Hemolytic Anemia 63 0.031
292
c GLC092 Glaucoma, Primary Open Angle 62 0.031
293
MDD011 Mood Disorder 62 0.031
294
P BLD124 Bleeding Disorder, Platelet-Type, 11 62 0.031
295
P PLM036 Pulmonary Fibrosis 62 0.031
296
NTR005 Nutritional Deficiency Disease 62 0.031
297
c BRN108 Branchiootic Syndrome 1 61 0.031
298
P LPS004 Lupus Erythematosus 61 0.031
299
OST003 Osteonecrosis 61 0.031
300
LNG099 Lung Disease 61 0.031
301
P SNS001 Sensorineural Hearing Loss 61 0.031
302
LBR030 Leber Optic Atrophy 61 0.031
303
ACN002 Acanthosis Nigricans 61 0.031
304
RGH009 Right Atrial Isomerism 61 0.031
305
P MYL006 Myeloid Leukemia 60 0.031
306
RTN017 Retinal Detachment 60 0.031
307
SQM006 Squamous Cell Carcinoma 60 0.031
308
ASP002 Aspartylglucosaminuria 60 0.031
309
HYD002 Hydronephrosis 60 0.031
310
P MLN069 Melanoma, Uveal 60 0.031
311
P SCL018 Scoliosis 60 0.031
312
STT001 Status Epilepticus 60 0.031
313
P WLF004 Wolfram Syndrome 60 0.031
314
P CYS018 Cystitis 60 0.031
315
P BND020 Bone Disease 60 0.031
316
P SYP003 Syphilis 60 0.031
317
P TRC086 Trichohepatoenteric Syndrome 1 59 0.031
318
CRY035 Cryptorchidism, Unilateral or Bilateral 59 0.031
319
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 59 0.031
320
CHL123 Chlamydia 59 0.031
321
PLM033 Pulmonary Embolism 59 0.031
322
HLC007 Helicobacter Pylori Infection 59 0.031
323
ANT024 Anthrax Disease 59 0.031
324
IRN001 Iron Deficiency Anemia 59 0.031
325
ADN018 Adenoma 59 0.031
326
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 59 0.031
327
EYD002 Eye Disease 59 0.031
328
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 59 0.031
329
P AXN002 Axenfeld-Rieger Syndrome 58 0.031
330
END030 End Stage Renal Failure 58 0.031
331
c DWL002 Dowling-Degos Disease 1 58 0.031
332
P CND004 Candidiasis 58 0.031
333
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 58 0.031
334
LYM027 Lymphopenia 58 0.031
335
EMB004 Embryonal Carcinoma 58 0.031
336
P DNG005 Dengue Virus 58 0.031
337
BLR008 Bilirubin Metabolic Disorder 58 0.031
338
PLG002 Plague 57 0.031
339
P SHR029 Short Syndrome 57 0.031
340
P GLM007 Glomerulonephritis 57 0.031
341
AGN016 Aging 56 0.031
342
SML019 Smallpox 56 0.031
343
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.031
344
P PLY011 Polycystic Ovary Syndrome 56 0.031
345
MTH009 Mouth Disease 56 0.031
346
HPT022 Hepatoblastoma 56 0.031
347
SYN007 Synovitis 56 0.031
348
BRN004 Brain Edema 56 0.031
349
c SVR001 Severe Acute Respiratory Syndrome 56 0.031
350
ICH001 Ichthyosis Vulgaris 56 0.031
351
HRY003 Hairy Cell Leukemia 55 0.031
352
ACT058 Active Peptic Ulcer Disease 55 0.031
353
FLR002 Filariasis 55 0.031
354
P FTL001 Fetal Alcohol Syndrome 55 0.031
355
ACT200 Acute Monoblastic Leukemia 55 0.031
356
TNG003 Tongue Cancer 55 0.031
357
P LYM031 Lymphocytic Leukemia 55 0.031
358
P SBS003 Substance Abuse 55 0.031
359
PRT038 Protein-Energy Malnutrition 55 0.031
360
CLL003 Cellulitis 55 0.031
361
HYP060 Hyperinsulinism 55 0.031
362
P MCR010 Microcephaly 55 0.031
363
JPN002 Japanese Encephalitis 54 0.031
364
P LRY044 Larynx Cancer 54 0.031
365
c CNT035 Central Nervous System Disease 54 0.031
366
P MNC007 Monocytic Leukemia 54 0.031
367
c LKM070 Leukemia, Acute Monocytic 54 0.031
368
KRT006 Keratoconjunctivitis 54 0.031
369
MST005 Mastitis 53 0.031
370
HMC014 Homocysteinemia 53 0.031
371
TRM010 Traumatic Brain Injury 53 0.031
372
CLF001 Cleft Lip 53 0.031
373
THR013 Thoracic Outlet Syndrome 53 0.031
374
c MCR113 Microvascular Complications of Diabetes 3 53 0.031
375
DRM011 Dermatophytosis 53 0.031
376
P SML001 Small Cell Carcinoma 53 0.031
377
P PTS002 Ptosis 53 0.031
378
IMP005 Impotence 52 0.031
379
TXC002 Toxic Encephalopathy 52 0.031
380
HYP014 Hyperuricemia 52 0.031
381
P NRC002 Narcolepsy 52 0.031
382
THR016 Thrombophlebitis 52 0.031
383
MYL001 Myelitis 51 0.031
384
RTN003 Retinal Ischemia 51 0.031
385
ADT003 Auditory System Disease 51 0.031
386
AZS001 Azoospermia 51 0.031
387
c HLP024 Holoprosencephaly 2 51 0.031
388
CYS008 Cystic Echinococcosis 51 0.031
389
CCC002 Coccidiosis 50 0.031
390
FLR001 Filarial Elephantiasis 50 0.031
391
TRY001 Trypanosomiasis 50 0.031
392
P CHR345 Chronic Pain 50 0.031
393
CRV040 Cervix Carcinoma 50 0.031
394
P RNL007 Renal Tubular Acidosis 50 0.031
395
AMB002 Amblyopia 50 0.031
396
HYP017 Hypophosphatemia 50 0.031
397
P KRT007 Keratoconus 50 0.031
398
PLC008 Placenta Disease 50 0.031
399
AMB001 Amebiasis 49 0.031
400
P OPN001 Open-Angle Glaucoma 49 0.031
401
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 49 0.031
402
PPL021 Papilledema 49 0.031
403
RDC002 Radiculopathy 49 0.031
404
P CMP008 Compartment Syndrome 49 0.031
405
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.031
406
CCN002 Cocaine Abuse 48 0.031
407
P ALP106 Alport Syndrome 1, X-Linked 48 0.031
408
P END046 Endometritis 48 0.031
409
c MCR120 Microvascular Complications of Diabetes 7 47 0.031
410
P TCL004 T-Cell Leukemia 47 0.031
411
HYP082 Hypopharynx Cancer 47 0.031
412
P BLD051 Blood Coagulation Disease 47 0.031
413
LYM009 Lymphocytic Choriomeningitis 47 0.031
414
P MYC033 Myoclonus 46 0.031
415
ENC010 Encephalocraniocutaneous Lipomatosis 46 0.031
416
P MTH007 Methemoglobinemia 46 0.031
417
P TRN034 Transverse Myelitis 46 0.031
418
CHL147 Chlamydia Pneumonia 46 0.031
419
GLL048 Glial Tumor 46 0.031
420
HDN002 Head Injury 46 0.031
421
PRL019 Prolidase Deficiency 46 0.031
422
P BNG032 Benign Mesothelioma 45 0.031
423
RTR001 Retrograde Amnesia 45 0.031
424
CLD007 Cold Agglutinin Disease 45 0.031
426
CRB008 Cerebral Atherosclerosis 44 0.031
427
CRT015 Carotid Artery Occlusion 44 0.031
428
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.031
429
CHL109 Childhood Apraxia of Speech 44 0.031
430
c RTN047 Retinitis Pigmentosa 18 44 0.031
431
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 44 0.031
432
VRL003 Variola Major 44 0.031
433
SCT002 Scotoma 43 0.031
434
c FTL006 Fetal Alcohol Spectrum Disorder 43 0.031
435
HMP009 Haemophilus Influenzae 43 0.031
436
ALC010 Alcoholic Cardiomyopathy 43 0.031
437
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.031
438
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.031
439
MLK003 Melkersson-Rosenthal Syndrome 42 0.031
440
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.031
441
P CRN035 Cranial Nerve Palsy 42 0.031
442
c PST022 Posterior Uveal Melanoma 42 0.031
443
c MCR130 Microvascular Complications of Diabetes 6 41 0.031
444
c MCR133 Microvascular Complications of Diabetes 4 41 0.031
445
ACT088 Acute Insulin Response 41 0.031
446
ADJ001 Adjustment Disorder 41 0.031
447
PSD001 Pseudobulbar Palsy 41 0.031
448
ACT209 Acatalasemia 40 0.031
449
ELP001 Elephantiasis 40 0.031
450
KLD004 Keloid Disorder 40 0.031
451
P TRC031 Trichorhinophalangeal Syndrome 40 0.031
452
DBT007 Diabetic Cataract 40 0.031
453
PRM020 Premenstrual Tension 39 0.031
454
LYM014 Lymphangitis 39 0.031
455
ALC005 Alcoholic Pancreatitis 39 0.031
456
SPP007 Suppression Amblyopia 39 0.031
457
NDL024 Nodal Marginal Zone Lymphoma 39 0.031
458
SPS019 Spastic Paraparesis 39 0.031
459
PRM024 Primary Angle-Closure Glaucoma 39 0.031
460
MCP033 Mucopolysaccharidoses 38 0.031
461
FST001 Foster-Kennedy Syndrome 38 0.031
462
STR077 Streptococcal Toxic-Shock Syndrome 37 0.031
463
MYC017 Mycobacterium Kansasii 37 0.031
464
PCD001 Pica Disease 37 0.031
465
ATX010 Ataxia Neuropathy Spectrum 37 0.031
466
SYS071 Systemic Autoimmune Disease 37 0.031
467
LCH001 Leech Infestation 36 0.031
468
CRB009 Cerebritis 36 0.031
469
P PLM149 Palmoplantar Keratoderma and Congenital Alopecia 2 36 0.031
471
c CHR087 Chronic Cystitis 35 0.031
472
P HRD217 Hereditary Optic Neuropathy 35 0.031
473
PPL052 Papillomatosis, Confluent and Reticulated 34 0.031
474
c ART068 Aortic Aneurysm, Familial Thoracic 2 34 0.031
475
AMN014 Aminopterin Syndrome Sine Aminopterin 33 0.031
476
ALR002 Al-Raqad Syndrome 33 0.031
477
ACT064 Acute Necrotizing Encephalitis 32 0.031
478
NRN002 Neuronitis 32 0.031
479
MYC015 Mycobacterium Fortuitum 31 0.031
480
MYC088 Mycobacterium Avium Complex Infections 30 0.031
481
c BLD140 Blood Group, I System 29 0.031
482
ACT038 Acute Retrobulbar Neuritis 29 0.031
483
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.031
484
BNG077 Benign Idiopathic Neonatal Seizures 27 0.031
485
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.031
486
EPL050 Epilepsy, Partial, with Pericentral Spikes 25 0.031
487
SST003 Sister Chromatid Exchange, Frequency of 24 0.031
488
GNT018 Gianotti Crosti Syndrome 24 0.031
489
P SLF001 Sulfhemoglobinemia 23 0.031
490
PLS037 Plasma Cell Tumor 22 0.031
491
BLD165 Blood Group, Colton System 21 0.031
492
AND005 Androgen Insensitivity Syndrome, Mild 19 0.031
493
PNT023 Pontine Hemorrhage 17 0.031
494
BLD137 Blood Group--Ahonen 16 0.031
495
OBS524 Obsolete: Benign Exophthalmos Syndrome 13 0.031
496
FRM006 Formaldehyde Poisoning 11 0.031
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