Search results for Salicylic acid

737 hits were found for Salicylic acid

# Family MCID Name MIFTS Score
1
c NRF023 Neurofibromatosis, Type Ii 80 0.326
2
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.296
3
P LVR013 Liver Disease 68 0.287
4
MTB004 Metabolic Acidosis 50 0.287
5
P PSR002 Psoriasis 62 0.284
6
PST011 Pustulosis of Palm and Sole 52 0.281
7
FTT001 Fatty Liver Disease 61 0.254
8
OST012 Osteoarthritis 78 0.252
9
ULC004 Ulcerative Colitis 73 0.248
10
48X005 48,xyyy 39 0.248
11
DRM006 Dermatitis 61 0.248
12
P CLR023 Colorectal Cancer 99 0.248
13
CLT003 Colitis 62 0.245
14
P KDN018 Kidney Disease 72 0.242
15
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.242
16
HYP056 Hypoglycemia 66 0.242
17
ENT004 Enthesopathy 49 0.227
18
HLX001 Helix Syndrome 47 0.225
19
RYS001 Reye Syndrome 51 0.223
20
P INF037 Inflammatory Bowel Disease 54 0.221
21
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.220
22
P DRR001 Diarrhea 55 0.218
23
ALL026 Allergic Hypersensitivity Disease 62 0.216
24
RHM001 Rheumatic Fever 60 0.213
25
LVR012 Liver Cirrhosis 62 0.211
26
P SZR006 Seizure Disorder 56 0.206
27
ISC004 Ischemia 58 0.204
28
GT001 Gout 64 0.202
29
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.201
30
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.201
31
P ENC018 Encephalopathy 61 0.201
32
NRL016 Neural Tube Defects 82 0.201
33
P NRB001 Neuroblastoma 72 0.200
34
PLM010 Pulmonary Edema 54 0.199
35
P ART022 Arthritis 69 0.196
36
LPP008 Lipoprotein Quantitative Trait Locus 62 0.195
37
PLM001 Pulmonary Tuberculosis 69 0.195
38
VSL002 Visual Epilepsy 59 0.195
39
P RHM011 Rheumatoid Arthritis 80 0.194
40
HYP066 Hyperglycemia 61 0.193
41
KRT009 Keratosis 51 0.191
42
P CRN300 Coronary Heart Disease 1 63 0.190
43
BNR002 Bone Resorption Disease 48 0.189
44
PPT005 Peptic Ulcer Disease 59 0.187
45
P LKM002 Leukemia 68 0.185
46
P DDN001 Duodenal Ulcer 52 0.185
47
LPD008 Lipid Metabolism Disorder 62 0.184
48
P VSC007 Vascular Disease 63 0.183
49
P GST044 Gastritis 56 0.183
50
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.182
51
P BRS047 Breast Cancer 97 0.181
52
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.178
53
c PRC016 Pre-Eclampsia 63 0.178
54
OCL069 Ocular Motor Apraxia 51 0.178
55
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.178
56
DFC004 Deficiency Anemia 70 0.177
57
SKN016 Skin Disease 63 0.175
58
HRW001 Hair Whorl 36 0.175
59
P DBT009 Diabetes Mellitus 64 0.175
60
ATH013 Atherosclerosis Susceptibility 65 0.174
61
ART140 Arteries, Anomalies of 52 0.172
62
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.172
63
P GLM045 Glioma 63 0.172
64
CRH001 Crohn's Disease 74 0.172
65
P PRS040 Prostate Cancer 97 0.171
66
GLL048 Glial Tumor 45 0.170
67
P MYL006 Myeloid Leukemia 60 0.167
68
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.167
69
ATM095 Autoimmune Disease 62 0.165
70
P HPT023 Hepatocellular Carcinoma 100 0.165
71
CNT047 Contact Dermatitis 58 0.165
72
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.164
73
c DWL002 Dowling-Degos Disease 1 58 0.162
74
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.161
75
PRT037 Pertussis 65 0.157
76
c HYP836 Hypercholesterolemia, Familial, 1 73 0.156
77
P HRT032 Heart Disease 75 0.156
78
GLB015 Glioblastoma Multiforme 75 0.155
79
c HYP595 Hypertension, Essential 84 0.154
80
P CRD246 Cardiovascular System Disease 57 0.154
81
P ADN016 Adenocarcinoma 64 0.153
82
c GLL024 Gallbladder Disease 1 53 0.153
83
P MYC007 Myocardial Infarction 70 0.153
84
c FNC043 Fanconi Anemia, Complementation Group E 62 0.152
85
HYP060 Hyperinsulinism 54 0.152
86
P ALZ034 Alzheimer Disease 88 0.151
87
c CHR684 Chronic Kidney Disease 70 0.151
88
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.150
89
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.150
90
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.150
91
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.150
92
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.150
93
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.150
94
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.150
95
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.150
96
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.150
97
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.150
98
P URT039 Urticaria 58 0.148
99
P OST002 Osteoporosis 74 0.148
100
P OVR042 Ovarian Cancer 88 0.148
101
IRN002 Iron Metabolism Disease 57 0.146
102
DPR016 Depression 63 0.146
103
c LKM061 Leukemia, Acute Myeloid 84 0.144
104
P ACT008 Actinic Keratosis 53 0.144
105
HYP781 Hypoascorbemia 51 0.144
106
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.144
107
GST023 Gastric Ulcer 53 0.144
108
c JVN010 Juvenile Rheumatoid Arthritis 64 0.143
109
HYP266 Hypoxia 57 0.143
110
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.143
111
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.142
112
P RSP003 Respiratory Failure 74 0.142
113
CYT002 Cytokine Deficiency 42 0.141
114
P PNC035 Pancreatic Cancer 84 0.141
115
HMN044 Human Immunodeficiency Virus Type 1 71 0.140
116
ADN018 Adenoma 59 0.140
117
CRB039 Cerebrovascular Disease 67 0.140
118
P NRP001 Neuropathy 56 0.140
119
c ACT071 Acute Kidney Failure 60 0.140
120
NNL006 Non-Alcoholic Steatohepatitis 54 0.139
121
STR067 Stroke, Ischemic 81 0.139
122
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.139
123
47X002 47,xyy 49 0.139
124
THR024 Thrombosis 57 0.137
125
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.135
126
ALL010 Allergic Contact Dermatitis 56 0.135
127
P BLD134 Bladder Cancer 79 0.134
128
P TRN020 Turner Syndrome 67 0.133
129
P DRM053 Dermatitis, Atopic 66 0.133
130
MNT002 Mental Depression 58 0.132
131
c ACT075 Acute Myocardial Infarction 57 0.131
132
HPT004 Hepatic Coma 45 0.131
133
P PRD008 Periodontitis 64 0.131
134
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.131
135
c PCH010 Pachyonychia Congenita 3 44 0.130
136
P HPT021 Hepatitis 67 0.130
137
MYL069 Myeloma, Multiple 85 0.130
138
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.129
139
PRT036 Peritonitis 64 0.129
140
P SKN015 Skin Carcinoma 66 0.128
141
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.127
142
CHL014 Cholera 59 0.127
143
P THR014 Thrombocytopenia 67 0.126
144
PPL022 Papilloma 54 0.125
145
c THR092 Thrombophilia Due to Thrombin Defect 73 0.124
146
CNG034 Congestive Heart Failure 69 0.124
147
STT001 Status Epilepticus 60 0.124
148
c RHB024 Rhabdomyosarcoma 2 67 0.124
149
P HYP086 Hypothyroidism 69 0.124
150
ANX004 Anoxia 40 0.124
151
c DBT099 Diabetes Mellitus, Type I 65 0.124
152
SPN186 Spinal Cord Injury 60 0.123
153
LNG099 Lung Disease 60 0.123
154
ACT094 Acute Articular Rheumatism 26 0.123
155
P NTR004 Neutropenia 63 0.123
156
P CTR002 Cataract 60 0.123
157
HPT019 Hepatic Encephalopathy 60 0.123
158
AGN016 Aging 56 0.122
159
ALC007 Alcohol Dependence 66 0.121
160
URM002 Uremia 49 0.121
161
P ECL001 Eclampsia 50 0.120
162
PLM033 Pulmonary Embolism 59 0.120
163
ADL002 Adult Syndrome 70 0.119
164
P MJR001 Major Depressive Disorder 68 0.119
165
P MLN008 Melanoma 69 0.119
166
BCT022 Bacterial Infectious Disease 56 0.119
167
CRB004 Cerebral Artery Occlusion 45 0.118
168
MYL009 Myelodysplastic Syndrome 70 0.118
169
SQM002 Squamous Cell Papilloma 46 0.118
170
P OVR082 Overgrowth Syndrome 50 0.118
171
c ACT027 Acute Pancreatitis 60 0.118
172
GLC003 Glucose Intolerance 54 0.118
173
END086 End Stage Renal Disease 51 0.118
174
P PNC044 Pancreatitis 61 0.117
175
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.117
176
AST005 Asthma 76 0.117
177
NTR005 Nutritional Deficiency Disease 62 0.117
178
P HRP006 Herpes Simplex 65 0.117
179
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.116
180
HYP005 Hypokalemia 55 0.116
181
P MNN013 Meningitis 66 0.116
182
P GST053 Gastric Cancer 83 0.116
183
PPL052 Papillomatosis, Confluent and Reticulated 33 0.116
184
SQM006 Squamous Cell Carcinoma 60 0.115
185
P SCH015 Schizophrenia 74 0.115
186
P MYP004 Myopathy 70 0.114
187
TXC005 Toxic Shock Syndrome 62 0.113
188
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.113
189
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.112
190
c MGR028 Migraine with or Without Aura 1 67 0.112
191
NPH009 Nephrolithiasis 55 0.112
192
P MCR115 Microvascular Complications of Diabetes 5 66 0.111
193
c ACT068 Acute Cystitis 63 0.111
194
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.111
195
c SYS001 Systemic Lupus Erythematosus 86 0.111
196
ATX019 Ataxia with Vitamin E Deficiency 42 0.110
197
c MCR120 Microvascular Complications of Diabetes 7 47 0.110
198
P LPS004 Lupus Erythematosus 61 0.110
199
c MCR113 Microvascular Complications of Diabetes 3 52 0.110
200
TRM010 Traumatic Brain Injury 51 0.110
201
STM007 Stomatitis 50 0.110
202
c MCR130 Microvascular Complications of Diabetes 6 41 0.109
203
c MCR133 Microvascular Complications of Diabetes 4 41 0.109
204
DBT010 Diabetic Neuropathy 54 0.109
205
P PRP019 Peripheral Nervous System Disease 58 0.109
206
DWN001 Down Syndrome 70 0.109
207
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.108
208
P RHN004 Rhinitis 57 0.108
209
PNG002 Pain Agnosia 51 0.108
210
PRP030 Purpura 54 0.107
211
P ART021 Arteriosclerosis 54 0.107
212
BLR008 Bilirubin Metabolic Disorder 57 0.106
213
SBC016 Subacute Delirium 44 0.106
214
ALL014 Allergic Encephalomyelitis 38 0.106
215
P TRM003 Tremor 54 0.106
216
P RTN024 Retinoblastoma 73 0.105
217
P EXN002 Exanthem 57 0.105
218
IMM167 Immune Deficiency Disease 78 0.105
219
c FML008 Familial Retinoblastoma 53 0.105
220
P HYP076 Hyperthyroidism 55 0.104
221
P ADL010 Adult Respiratory Distress Syndrome 65 0.104
222
c LKM063 Leukemia, Chronic Myeloid 72 0.104
223
P INF032 Infertility 57 0.103
224
P HDC001 Headache 57 0.103
225
P CHR345 Chronic Pain 44 0.103
226
P AST007 Astrocytoma 51 0.103
227
P LKM071 Leukemia, Chronic Lymphocytic 79 0.103
228
c PSR017 Psoriasis 2 53 0.102
229
c PSR023 Psoriasis 1 52 0.102
230
c PSR032 Psoriasis 11 47 0.102
231
c PSR028 Psoriasis 7 42 0.102
232
c PSR018 Psoriasis 13 41 0.102
233
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.102
234
P ART023 Arthropathy 62 0.101
235
CLN015 Colon Adenocarcinoma 65 0.101
236
VCC001 Vaccinia 49 0.101
237
DWR001 Dwarfism 44 0.100
238
PRP027 Peripheral Vascular Disease 71 0.100
239
c BRN108 Branchiootic Syndrome 1 62 0.100
240
RSC001 Rosacea 54 0.100
241
c ACT073 Acute Leukemia 58 0.099
242
P BCL017 B-Cell Lymphoma 58 0.099
243
ANG054 Angina Pectoris 66 0.099
244
P CNR004 Cone-Rod Dystrophy 2 73 0.099
245
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.098
246
P ENC004 Encephalitis 61 0.098
247
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.098
248
c VRL010 Viral Hepatitis 52 0.098
249
THY029 Thyroid Carcinoma 59 0.098
250
P TMP001 Temporal Lobe Epilepsy 50 0.098
251
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.097
252
SYN007 Synovitis 54 0.097
253
PLC002 Plica Syndrome 36 0.097
254
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.097
255
P PRP029 Porphyria 62 0.097
256
ANX010 Anxiety 73 0.097
257
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.097
258
P PLY019 Polyneuropathy 56 0.096
259
c ACT134 Acute Liver Failure 56 0.096
260
KWS002 Kawasaki Disease 65 0.096
261
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.096
262
ACQ007 Acquired Immunodeficiency Syndrome 60 0.096
263
URL001 Urolithiasis 45 0.096
264
BRN024 Bronchitis 68 0.096
265
DNT012 Dental Caries 53 0.095
266
CLF027 Cleft Palate, Isolated 64 0.094
267
P END033 Endocarditis 57 0.094
268
KRT013 Keratolytic Winter Erythema 46 0.094
269
MLR004 Malaria 81 0.094
270
P MLT020 Multiple Sclerosis 72 0.094
271
P LNG064 Lung Cancer Susceptibility 3 78 0.093
272
P INS002 in Situ Carcinoma 53 0.093
273
GNG013 Gingivitis 59 0.093
274
GST050 Gastrointestinal System Disease 56 0.092
276
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.092
277
ESP021 Esophageal Cancer 90 0.092
278
P SNS001 Sensorineural Hearing Loss 60 0.091
279
ALL003 Allergic Rhinitis 67 0.091
280
P INF038 Influenza 68 0.091
281
P FBR017 Fibrosarcoma 56 0.091
282
P PLY011 Polycystic Ovary Syndrome 56 0.091
283
P MYC084 Mycobacterium Tuberculosis 1 68 0.091
284
c CHR064 Chronic Monocytic Leukemia 33 0.091
285
PSY004 Psychotic Disorder 67 0.090
286
FDL002 Food Allergy 51 0.090
287
MCS002 Mucositis 56 0.090
288
P ALP008 Alopecia 54 0.090
289
P ATR011 Atrial Fibrillation 66 0.090
290
BRN004 Brain Edema 56 0.089
291
DPH001 Diphtheria 60 0.089
292
P PNM007 Pneumonia 68 0.088
293
P CRD119 Cardiac Arrest 67 0.088
294
P ICH004 Ichthyosis 54 0.088
295
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.088
296
CHL079 Children's Interstitial Lung Disease 26 0.088
297
P ALC033 Alcohol Use Disorder 58 0.087
298
MLN073 Melanosis, Neurocutaneous 45 0.087
299
P AMY004 Amyloidosis 70 0.087
300
CMM005 Common Cold 57 0.087
301
P BRS044 Breast Adenocarcinoma 59 0.087
302
P HYP098 Hypereosinophilic Syndrome 67 0.086
303
CHR073 Choreatic Disease 52 0.086
304
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.086
305
c PRS136 Prostate Cancer, Hereditary, 6 33 0.085
306
c PRS130 Prostate Cancer, Hereditary, 8 32 0.085
307
HYP144 Hyperacusis 23 0.085
308
END057 Endometrial Cancer 74 0.085
309
KRT019 Keratitis, Hereditary 65 0.084
310
HMS001 Hemosiderosis 54 0.083
311
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.083
312
TYP007 Typhoid Fever 63 0.083
313
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.083
314
c HPT003 Hepatitis a 62 0.083
315
NTR046 Neutrophil Migration 50 0.083
316
END040 Endogenous Depression 55 0.083
317
c PNS012 Paine Syndrome 61 0.082
318
CRH005 Crohn's Colitis 53 0.082
319
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.082
320
P RRH023 Rare Hereditary Hemochromatosis 41 0.082
321
LPT014 Leptin Deficiency or Dysfunction 74 0.081
322
P SYS005 Systemic Scleroderma 68 0.081
323
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.081
324
INT007 Intermediate Coronary Syndrome 55 0.081
325
ORL011 Oral Cancer 60 0.080
326
TRN015 Transient Cerebral Ischemia 63 0.080
327
ERY051 Erythroleukemia, Familial 56 0.080
328
LSH001 Leishmaniasis 63 0.080
329
MST005 Mastitis 53 0.080
330
P KLZ004 Kala-Azar 1 41 0.080
331
ALL006 Allergic Asthma 56 0.079
332
NRT001 Neurotic Disorder 53 0.079
333
KWS001 Kwashiorkor 44 0.079
334
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.079
335
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.078
336
ADG002 Audiogenic Seizures 25 0.078
337
DSS009 Disseminated Intravascular Coagulation 57 0.078
338
TLN003 Telangiectasis 52 0.078
339
PRC013 Pericarditis 54 0.078
340
P PLM037 Pulmonary Hypertension 67 0.078
341
P ANG015 Angioedema 57 0.077
342
PLN001 Plantar Wart 34 0.077
343
ORL015 Oral Squamous Cell Carcinoma 43 0.077
344
HYP081 Hypolipoproteinemia 51 0.077
345
P MYC008 Myocarditis 59 0.077
346
CHR100 Chronic Ulcer of Skin 55 0.077
347
PLM031 Poliomyelitis 64 0.077
348
c BSL007 Basal Cell Carcinoma 68 0.077
349
ANR040 Aneurysm 59 0.077
350
P HML002 Hemolytic Anemia 63 0.076
351
AMN006 Aminoaciduria 38 0.076
352
CLR108 Colorectal Adenoma 64 0.076
353
P CND004 Candidiasis 58 0.076
354
CHC001 Chickenpox 60 0.076
355
DSS008 Disease of Mental Health 58 0.076
356
P NRV007 Nervous System Disease 66 0.075
357
MSL001 Measles 62 0.075
358
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.075
359
P SBR004 Seborrheic Dermatitis 45 0.075
360
INT002 Intermittent Claudication 61 0.075
361
P SLP006 Sleep Apnea 69 0.074
362
c MCR129 Microvascular Complications of Diabetes 1 66 0.074
363
P END044 Endometriosis 63 0.074
364
PLC008 Placenta Disease 50 0.074
365
PLR008 Pleurisy 50 0.074
366
PLG002 Plague 63 0.074
367
SKN019 Skin Melanoma 68 0.074
368
P INT068 Intestinal Disease 53 0.073
369
IGR001 Ige Responsiveness, Atopic 59 0.073
370
SPL018 Splenomegaly 48 0.073
371
P KDN017 Kidney Cancer 60 0.072
372
TBR011 Tuberculous Meningitis 48 0.072
373
CHL056 Cheilitis 48 0.072
374
PRP080 Peripheral Artery Disease 53 0.072
375
P SCK005 Sickle Cell Disease 50 0.072
376
c INF071 Inflammatory Bowel Disease 1 67 0.071
377
P ANP001 Anaplastic Large Cell Lymphoma 58 0.071
378
OST017 Osteomyelitis 64 0.071
379
P THY032 Thyroiditis 52 0.070
380
P SYP003 Syphilis 58 0.070
381
P PRC031 Preeclampsia/eclampsia 1 38 0.070
382
RFR010 Refractory Anemia 48 0.069
383
c PRD040 Periodontitis, Chronic 53 0.069
384
P ANT006 Antiphospholipid Syndrome 55 0.069
385
c FML035 Familial Hyperlipidemia 55 0.069
386
PRP016 Paraplegia 52 0.068
387
PST092 Posttransplant Acute Limbic Encephalitis 29 0.068
388
CHL067 Cholecystitis 57 0.068
389
HDN002 Head Injury 46 0.068
390
VRC005 Varicose Veins 60 0.067
391
HVY002 Heavy Metal Poisoning 22 0.067
392
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.067
393
HRN029 Hearing Loss, Noise-Induced 37 0.067
394
MSC007 Muscle Hypertrophy 64 0.067
395
MYL031 Myeloproliferative Neoplasm 66 0.067
396
P CHR285 Chronic Myelomonocytic Leukemia 60 0.067
397
c SVR005 Severe Pre-Eclampsia 50 0.067
398
PRD004 Prediabetes Syndrome 47 0.067
399
P MVM001 Movement Disease 63 0.066
400
INT067 Interstitial Nephritis 48 0.066
401
49X006 49, Xxxxy Syndrome 41 0.066
402
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.066
403
P RNL007 Renal Tubular Acidosis 51 0.066
404
RDN001 Reading Disorder 40 0.066
405
P SRC025 Sarcoidosis 1 70 0.066
406
ANR007 Anorexia Nervosa 63 0.065
407
CNN005 Connective Tissue Disease 68 0.065
408
c SPN225 Spondyloarthropathy 1 73 0.065
409
P PLM034 Pulmonary Emphysema 55 0.065
410
P VSC011 Vasculitis 62 0.064
411
P RHB003 Rhabdomyosarcoma 63 0.064
412
CLR109 Colorectal Adenocarcinoma 51 0.064
413
c HNT004 Huntington Disease-Like 2 50 0.064
414
c HNT011 Huntington Disease-Like 3 38 0.064
415
DRM011 Dermatophytosis 52 0.064
416
LNT004 Lentigines 50 0.064
417
CRT017 Cartilage Disease 54 0.064
418
c GRV008 Graves Disease 1 56 0.063
419
CLF001 Cleft Lip 53 0.063
420
OVR094 Ovarian Epithelial Cancer 38 0.062
421
NNT012 Neonatal Jaundice 53 0.062
422
P FNC004 Fanconi Syndrome 50 0.062
423
HND015 Hand Skill, Relative 33 0.062
424
BNM001 Bone Marrow Cancer 43 0.061
425
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.061
426
SPN051 Spondylitis 51 0.061
427
INF009 Inflammatory Spondylopathy 31 0.061
428
VRL011 Viral Infectious Disease 61 0.060
429
P FNC034 Fanconi Renotubular Syndrome 2 40 0.060
430
PLC007 Placental Abruption 48 0.060
431
MYC015 Mycobacterium Fortuitum 32 0.060
432
HYD002 Hydronephrosis 60 0.060
433
P OPN001 Open-Angle Glaucoma 49 0.060
434
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.060
435
HYP017 Hypophosphatemia 50 0.060
436
c FML001 Familial Atrial Fibrillation 65 0.059
437
c BCT007 Bacterial Meningitis 55 0.059
438
THR004 Thrombocytosis 51 0.059
439
P BRB001 Beriberi 46 0.059
441
IRR003 Irritant Dermatitis 49 0.059
442
FBR047 Fibromyalgia 58 0.058
443
P LCH002 Lichen Planus 53 0.058
444
THY030 Thyroid Gland Disease 52 0.058
445
MLL001 Molluscum Contagiosum 50 0.058
446
INT030 Intracranial Aneurysm 56 0.058
447
P ATX030 Ataxia-Telangiectasia 82 0.058
448
PNM008 Pneumothorax 56 0.058
449
ATN004 Autonomic Neuropathy 45 0.058
450
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.058
451
ASP030 Aspirin Resistance 39 0.057
452
TNS005 Tonsillitis 57 0.057
453
PPL049 Papillon-Lefevre Syndrome 65 0.057
454
YLL002 Yellow Fever 61 0.057
455
GLS018 Glass Syndrome 57 0.057
456
c SBR001 Seborrheic Infantile Dermatitis 30 0.057
457
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.057
458
TRD006 Tardive Dyskinesia 54 0.057
459
SLP001 Sleeping Sickness 54 0.057
460
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.057
461
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.057
462
MLC004 Mulchandani-Bhoj-Conlin Syndrome 44 0.057
463
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.056
464
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.056
465
SDD001 Sudden Infant Death Syndrome 61 0.056
466
LMB062 Limb Ischemia 55 0.056
467
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.056
468
ATY042 Atypical Chronic Myeloid Leukemia 49 0.056
469
P OVR046 Ovarian Cyst 47 0.055
470
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.055
471
HYP043 Hyperandrogenism 48 0.055
472
c PLY105 Polycystic Ovary Syndrome 1 38 0.055
473
BLD053 Blood Platelet Disease 49 0.055
474
ACT088 Acute Insulin Response 41 0.055
475
SPP011 Suppression of Tumorigenicity 12 59 0.055
476
ACT003 Acute Kidney Tubular Necrosis 45 0.055
477
P DRM010 Dermatomyositis 61 0.054
478
ALP077 Alpha-Methylacetoacetic Aciduria 55 0.054
479
c LPM012 Lipomatosis, Multiple 60 0.054
480
CRB086 Cerebral Aneurysms 40 0.054
481
P MYS003 Myasthenia Gravis 68 0.054
482
ETN001 Eating Disorder 60 0.054
483
RSP006 Respiratory System Disease 50 0.054
484
SCH003 Schizophreniform Disorder 56 0.054
485
P FBR031 Febrile Seizures 53 0.054
487
P PRG092 Pregnancy Loss, Recurrent 1 40 0.054
488
ERY003 Erythema Multiforme 58 0.054
489
P MMP001 Mumps 58 0.053
490
PTH003 Pathologic Nystagmus 52 0.053
491
BCK006 Back Pain 42 0.053
492
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.053
493
SPT004 Septic Arthritis 58 0.053
494
HMR039 Hemorrhage, Intracerebral 57 0.053
495
PFF001 Pfeiffer Syndrome 79 0.053
496
c GLC092 Glaucoma, Primary Open Angle 62 0.052
497
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.052
498
FNG017 Fungal Infectious Disease 53 0.052
499
P CLL015 Collagen Disease 47 0.052
500
HRT012 Heart Valve Disease 53 0.052
501
TST014 Testicular Cancer 46 0.052
502
P RBL001 Rubella 59 0.052
503
ATN005 Autonomic Dysfunction 46 0.052
504
RNL012 Renal Tuberculosis 33 0.052
505
PSR001 Psoriatic Arthritis 61 0.052
506
THY122 Thyroid Gland Cancer 57 0.052
507
P MRC003 Mercury Poisoning 48 0.052
508
SVR097 Severe Cutaneous Adverse Reaction 69 0.052
509
RHM028 Rheumatic Heart Disease 53 0.052
510
THR016 Thrombophlebitis 51 0.052
511
GST020 Gastric Antral Vascular Ectasia 41 0.052
512
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.051
513
P INT070 Intestinal Obstruction 58 0.051
514
P VTR007 Vitreoretinopathy 46 0.051
515
P MLG056 Malignant Hyperthermia 67 0.051
516
c JVN061 Juvenile Arthritis 60 0.051
517
P HYP040 Hypospadias 51 0.051
518
ERY066 Erythema Multiforme Major 30 0.051
519
PRC003 Proctitis 47 0.051
520
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 37 0.051
521
c CHR418 Chronic Leukemia 49 0.051
522
NRM005 Neuromuscular Disease 64 0.050
523
RTN020 Retinal Vascular Disease 46 0.050
524
HYP457 Hypertrophic Scars 42 0.050
525
c HMP029 Hemophilia a 67 0.050
526
P VNW001 Von Willebrand's Disease 65 0.050
527
P PTS002 Ptosis 53 0.050
528
c OVR114 Ovarian Cancer 1 38 0.050
529
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.050
530
P PRM002 Primary Hyperoxaluria 62 0.050
531
TXC002 Toxic Encephalopathy 53 0.050
532
P TCD001 Tic Disorder 53 0.050
533
TRP009 Triple X Syndrome 42 0.049
534
P MST009 Mastocytosis 64 0.048
535
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.048
536
BWN001 Bowen-Conradi Syndrome 52 0.048
537
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.048
538
TTH007 Tooth Erosion 31 0.048
539
INF034 Infective Endocarditis 53 0.048
540
TTH006 Tooth Disease 46 0.048
541
FRZ001 Frozen Shoulder 53 0.048
542
QDR001 Quadriplegia 48 0.048
543
MYL005 Myelofibrosis 70 0.048
544
CRN017 Coronary Thrombosis 47 0.048
545
CLN045 Colonic Benign Neoplasm 46 0.048
546
MNG007 Manganese Poisoning 29 0.048
547
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.047
548
CLS047 Classic Progressive Supranuclear Palsy Syndrome 31 0.047
549
LYM021 Lymphadenitis 57 0.047
550
APN008 Apnea, Obstructive Sleep 64 0.047
551
ICH001 Ichthyosis Vulgaris 55 0.047
552
P VNS003 Venous Insufficiency 55 0.047
553
DCT002 Ductal Carcinoma in Situ 59 0.046
554
P DBT005 Diabetes Insipidus 55 0.046
555
SNL007 Senile Cataract 42 0.046
556
c ATS307 Autosomal Recessive Cerebellar Ataxia 42 0.046
557
MST020 Mast Cell Activation Syndrome 26 0.046
558
BRS064 Bursitis 48 0.046
559
CHK001 Chikungunya 57 0.046
560
ORL005 Oral Candidiasis 56 0.046
561
OST011 Osteomalacia 52 0.046
562
ABD010 Abdominal Wall Defect 36 0.046
563
P PRC012 Pericardial Effusion 51 0.045
564
HMP001 Hemopericardium 48 0.045
565
CYN002 Cyanosis, Transient Neonatal 45 0.045
566
MRS001 Marasmus 42 0.045
567
BRY001 Berylliosis 40 0.045
568
P LRY019 Laryngitis 52 0.045
569
BRN014 Bronchopneumonia 54 0.044
570
DDN006 Duodenitis 49 0.044
571
INT078 Intracranial Thrombosis 49 0.044
572
AMN014 Aminopterin Syndrome Sine Aminopterin 33 0.044
573
ART002 Arts Syndrome 64 0.044
574
DCB001 Decubitus Ulcer 61 0.044
575
LTH004 Lathyrism 16 0.044
576
P PLY041 Polymyositis 57 0.043
577
APH001 Aphthous Stomatitis 57 0.043
578
ASP003 Aseptic Meningitis 51 0.043
579
CRV040 Cervix Carcinoma 51 0.043
580
ANT066 Anterior Cutaneous Nerve Entrapment Syndrome 34 0.043
581
P HRD008 Hereditary Hemorrhagic Telangiectasia 63 0.043
582
P CYS039 Cystic Kidney Disease 54 0.043
583
PYD002 Pyoderma 50 0.043
584
c BCT013 Bacterial Pneumonia 48 0.043
585
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 40 0.043
586
GLL008 Gilles De La Tourette Syndrome 66 0.042
587
c LKM070 Leukemia, Acute Monocytic 57 0.042
588
FLL008 Folliculitis 46 0.042
589
SKN005 Skin Atrophy 43 0.042
590
MTH086 Methotrexate Toxicity 33 0.042
591
c HYP768 Hyperlipoproteinemia, Type I 67 0.042
592
P STR020 Strabismus 55 0.042
593
P LCT002 Lactose Intolerance 53 0.042
594
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.042
595
RTR008 Root Resorption 45 0.042
596
MYF002 Myofascial Pain Syndrome 42 0.042
597
MCH006 Mechanical Strabismus 42 0.042
598
DRR014 Darier-White Disease 60 0.042
599
P BRT004 Bartter Disease 52 0.042
600
P HRD144 Hereditary Mixed Polyposis Syndrome 51 0.042
601
FSR001 Fusariosis 42 0.042
602
EPC002 Epicondylitis 41 0.042
603
c ATS013 Autosomal Recessive Congenital Ichthyosis 63 0.041
604
STP011 Stapes Ankylosis with Broad Thumbs and Toes 49 0.041
605
AST052 Asthma, Nasal Polyps, and Aspirin Intolerance 43 0.041
606
CRL001 Cerulean Cataract 27 0.041
607
ACT162 Acute Sensory Ataxic Neuropathy 26 0.041
608
TRG002 Trigeminal Neuralgia 60 0.041
609
P PTY003 Pityriasis Rubra Pilaris 58 0.041
610
OCL051 Ocular Tuberculosis 31 0.041
611
AYM001 Ayme-Gripp Syndrome 57 0.040
612
AMB002 Amblyopia 49 0.040
613
ART006 Arthus Reaction 44 0.040
614
SPP007 Suppression Amblyopia 39 0.040
615
PRC051 Paracetamol Poisoning 30 0.040
616
BRN038 Bronchial Disease 53 0.039
617
P RTN014 Retinal Artery Occlusion 47 0.039
618
BRN026 Branch Retinal Artery Occlusion 40 0.039
619
LYM017 Lyme Disease 64 0.039
620
P PTN014 Patent Ductus Arteriosus 1 60 0.039
621
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.039
622
GST009 Gastroschisis 53 0.039
623
CHR005 Chorioamnionitis 51 0.039
624
PLP001 Pulpitis 49 0.039
625
ANV001 Anovulation 47 0.039
626
AND014 Androgenic Alopecia 46 0.039
627
DRG024 Drug Allergy 42 0.039
628
FCL001 Facial Dermatosis 31 0.039
629
c SYS004 Systemic Mastocytosis 63 0.038
630
MTN003 Motion Sickness 53 0.038
631
MGK001 Megakaryocytic Leukemia 64 0.038
632
P ALP061 Alopecia, Androgenetic, 1 49 0.038
633
MLR002 Miliary Tuberculosis 49 0.038
634
TNP001 Tinea Pedis 46 0.038
636
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.038
637
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.037
638
KRT071 Keratosis, Seborrheic 58 0.037
639
CLC006 Calcinosis 48 0.037
640
DRM009 Dermatomycosis 36 0.037
641
MLG164 Malignant Epithelial Tumor of Ovary 26 0.037
642
c SBC007 Subacute Thyroiditis 45 0.037
643
PHT004 Photoallergic Dermatitis 28 0.037
644
P OVR049 Ovarian Disease 52 0.036
645
PRP017 Periapical Periodontitis 46 0.036
646
c CNT028 Central Retinal Artery Occlusion 43 0.036
647
ART008 Arteriosclerosis Obliterans 40 0.036
648
TMP019 Temporomandibular Joint Anomaly 28 0.036
649
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.035
650
AND020 Androgen Insensitivity, Partial 56 0.035
651
GLS007 Glossitis 47 0.035
652
c PRM093 Premature Ovarian Failure 7 47 0.035
653
STL007 Steel Syndrome 43 0.035
654
PYL002 Pylorospasm 27 0.035
655
HMR013 Hemorrhagic Proctocolitis 17 0.035
656
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 65 0.035
657
ORC001 Orchitis 46 0.035
658
FCL012 Facial Paralysis 46 0.035
659
ENM001 Enamel Caries 28 0.035
660
APL002 Aplasia of Lacrimal and Salivary Glands 57 0.034
661
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 55 0.034
662
EXF003 Exfoliative Dermatitis 27 0.034
663
THY020 Thyroid Hyalinizing Trabecular Adenoma 21 0.034
664
SCL001 Scalp Dermatosis 38 0.034
665
c CLR066 Ciliary Dyskinesia, Primary, 2 34 0.034
666
GRG001 Greig Cephalopolysyndactyly Syndrome 66 0.033
667
c HYP794 Hyperoxaluria, Primary, Type I 63 0.033
668
BLL003 Bell's Palsy 51 0.033
669
BRX001 Bruxism 50 0.033
670
c CHR431 Chronic Venous Insufficiency 49 0.033
671
OCL066 Oculogyric Crisis 38 0.033
672
PYR041 Pyruvate Kinase Deficiency of Red Cells 57 0.032
673
PLM029 Palmoplantar Keratosis 47 0.032
674
ESP027 Esophagus Squamous Cell Carcinoma 45 0.032
675
P DVL012 Developmental Dysplasia of the Hip 1 38 0.032
676
CNT060 Central Serous Chorioretinopathy 38 0.032
677
WLD005 Wild Type Attr Amyloidosis 32 0.032
678
EXT064 Extraoral Halitosis Due to Methanethiol Oxidase Deficiency 30 0.032
679
PND002 Pendred Syndrome 65 0.031
680
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 48 0.031
681
BP1002 Bap1 Tumor Predisposition Syndrome 42 0.031
682
PTY002 Pityriasis Versicolor 38 0.031
683
P DNT007 Dentin Sensitivity 36 0.031
684
DNT010 Dentin Caries 32 0.031
685
MTN002 Mite Infestation 32 0.031
686
BLP006 Blepharoconjunctivitis 31 0.031
687
P PRK001 Porokeratosis 55 0.030
688
P TRT019 Torticollis 48 0.030
689
ANL022 Anal Fistula 46 0.030
690
DNT014 Dental Pulp Disease 42 0.030
691
BKS003 Beukes Hip Dysplasia 41 0.030
692
DNT006 Dental Pulp Necrosis 41 0.030
693
BBN001 Bubonic Plague 41 0.030
694
TQP001 Taqi Polymorphism 32 0.030
695
c PCH015 Pachyonychia Congenita 1 59 0.029
696
MCR141 Mucormycosis 56 0.029
697
CPL003 Capillary Leak Syndrome 55 0.029
698
LMB002 Lambert-Eaton Myasthenic Syndrome 53 0.029
699
c ADM005 Adams-Oliver Syndrome 1 39 0.029
700
OST160 Osteoid Osteoma 37 0.029
701
HMR014 Hemorrhagic Shock and Encephalopathy Syndrome 17 0.029
702
P NNN008 Noonan Syndrome 1 76 0.027
703
P ECT006 Ectodermal Dysplasia 62 0.027
704
c LNG048 Long Qt Syndrome 3 53 0.027
705
MYC012 Mycetoma 49 0.027
706
MLT152 Multiple Self-Healing Squamous Epithelioma 47 0.027
707
c CHR056 Chronic Tic Disorder 43 0.027
708
PLG004 Plagiocephaly 41 0.027
709
TRC020 Tracheitis 36 0.027
710
P YWS001 Yaws 36 0.027
711
PPT002 Peptic Ulcer Perforation 36 0.027
712
HYP029 Hyperthyroxinemia 31 0.027
713
ASP036 Aspirin Allergy 30 0.027
714
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 68 0.026
715
TTH002 Tooth Agenesis 60 0.026
716
CHL028 Childhood Type Dermatomyositis 58 0.026
717
IND002 Indolent Systemic Mastocytosis 39 0.026
718
FCL011 Facial Nerve Disease 35 0.026
719
LMN011 Laminopathy 33 0.026
720
c ADM007 Adams-Oliver Syndrome 2 33 0.026
721
HYP645 Hyperthyroxinemia, Dystransthyretinemic 31 0.026
722
HRD216 Hereditary Palmoplantar Keratoderma 28 0.026
723
GNC005 Geniculate Ganglionitis 26 0.026
724
c PSD047 Pseudo-Turner Syndrome 21 0.026
725
CNG184 Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects 49 0.024
726
AND001 Anodontia 43 0.024
727
EPD070 Epidermoid Cysts 37 0.024
728
HMM002 Haim-Munk Syndrome 36 0.024
729
KNC002 Knuckle Pads 33 0.024
730
ALK023 Al Kaissi Syndrome 30 0.024
731
HYP823 Hypotonia, Ataxia, Developmental Delay, and Tooth Enamel Defect Syndrome 28 0.024
732
UTR057 Uterus Bicornis Bicollis with Partial Vaginal Septum and Unilateral Hematocolpos with Ipsilateral Renal Agenesis 28 0.024
733
P PNC113 Punctate Palmoplantar Keratoderma 24 0.024
734
AND017 Anodontia of Permanent Dentition 23 0.024
735
CHL131 Chlorpropamide-Alcohol Flushing 22 0.024
736
DBL008 Double Uterus-Hemivagina-Renal Agenesis 17 0.024
737
AQG004 Aquagenic Syringeal Acrokeratoderma 16 0.024
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