Search results for arachidonic acid

635 hits were found for arachidonic acid

# Family MCID Name MIFTS Score
1
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.394
2
PRT037 Pertussis 66 0.371
3
P LVR013 Liver Disease 71 0.307
4
P NRB010 Neuroblastoma 1 66 0.301
5
P CLR023 Colorectal Cancer 100 0.298
6
FTT001 Fatty Liver Disease 63 0.290
7
ISC004 Ischemia 62 0.277
8
P GLM045 Glioma 64 0.276
9
GLL048 Glial Tumor 48 0.273
10
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.264
11
LVR012 Liver Cirrhosis 67 0.263
12
P PSR002 Psoriasis 63 0.253
13
48X005 48,xyyy 37 0.249
14
PST011 Pustulosis of Palm and Sole 51 0.248
15
P KDN018 Kidney Disease 73 0.244
16
P INF037 Inflammatory Bowel Disease 57 0.243
17
P BPL003 Bipolar Disorder 59 0.243
18
c MJR024 Major Affective Disorder 9 42 0.242
19
c MJR022 Major Affective Disorder 8 39 0.242
20
P PRS040 Prostate Cancer 97 0.241
21
P CRN300 Coronary Heart Disease 1 59 0.237
22
ATH013 Atherosclerosis Susceptibility 68 0.232
23
P BRS047 Breast Cancer 99 0.232
24
CHL068 Cholestasis 61 0.229
25
BNR002 Bone Resorption Disease 51 0.229
26
P DRR001 Diarrhea 55 0.225
27
LPD008 Lipid Metabolism Disorder 64 0.224
28
c HYP836 Hypercholesterolemia, Familial, 1 74 0.218
29
CLT003 Colitis 63 0.217
30
P SZR006 Seizure Disorder 59 0.217
31
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.216
32
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.216
33
HYP066 Hyperglycemia 63 0.216
34
ALL026 Allergic Hypersensitivity Disease 65 0.215
35
ULC004 Ulcerative Colitis 75 0.214
36
P VSC007 Vascular Disease 65 0.214
37
VSL002 Visual Epilepsy 58 0.211
38
HLX001 Helix Syndrome 46 0.211
39
PLM017 Pulmonary Alveolar Microlithiasis 54 0.210
40
CHL014 Cholera 58 0.208
41
NRL016 Neural Tube Defects 83 0.207
42
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.206
43
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.204
44
P CRN018 Coronary Artery Anomaly 67 0.202
45
DRM006 Dermatitis 63 0.199
46
MTB004 Metabolic Acidosis 48 0.199
47
HYP266 Hypoxia 58 0.198
48
P DBT009 Diabetes Mellitus 66 0.198
49
CYS001 Cystic Fibrosis 84 0.197
50
OST012 Osteoarthritis 80 0.197
51
ART140 Arteries, Anomalies of 60 0.195
52
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.195
53
P ADN016 Adenocarcinoma 65 0.194
54
c ACT210 Acute Respiratory Distress Syndrome 59 0.191
55
GST092 Gastroesophageal Reflux 68 0.189
56
CYT002 Cytokine Deficiency 46 0.188
57
c GLL024 Gallbladder Disease 1 53 0.185
58
P HPT023 Hepatocellular Carcinoma 99 0.185
59
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.185
60
P ENC018 Encephalopathy 64 0.185
61
c PRC016 Pre-Eclampsia 63 0.185
62
HYP056 Hypoglycemia 68 0.184
63
P HYP750 Hypertriglyceridemia, Familial 62 0.184
64
P MYC007 Myocardial Infarction 74 0.183
65
GT001 Gout 63 0.183
66
P ALZ034 Alzheimer Disease 90 0.181
67
P LKM002 Leukemia 69 0.181
68
P HRT032 Heart Disease 78 0.179
69
ADN018 Adenoma 60 0.177
70
P FBR017 Fibrosarcoma 57 0.173
71
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.171
72
HMN044 Human Immunodeficiency Virus Type 1 73 0.171
73
ATM095 Autoimmune Disease 62 0.171
74
P MYL006 Myeloid Leukemia 61 0.169
75
SQM006 Squamous Cell Carcinoma 60 0.169
76
PPT005 Peptic Ulcer Disease 60 0.168
77
GLB002 Glioblastoma 74 0.167
78
CRH001 Crohn's Disease 75 0.167
79
GLB015 Glioblastoma Multiforme 60 0.166
80
c PCH010 Pachyonychia Congenita 3 43 0.165
81
HYP060 Hyperinsulinism 55 0.164
82
c ACT075 Acute Myocardial Infarction 59 0.164
83
OST159 Osteogenic Sarcoma 67 0.163
84
47X002 47,xyy 49 0.163
85
LNG099 Lung Disease 62 0.162
86
P LNG032 Lung Cancer 99 0.161
87
c HYP595 Hypertension, Essential 87 0.160
88
P PHC003 Pheochromocytoma 71 0.160
89
ADR040 Adrenal Gland Pheochromocytoma 51 0.160
90
c CHR684 Chronic Kidney Disease 68 0.159
91
CRB039 Cerebrovascular Disease 71 0.159
92
DFC004 Deficiency Anemia 77 0.158
93
P DRM053 Dermatitis, Atopic 68 0.158
94
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.157
95
P OVR042 Ovarian Cancer 89 0.156
96
P OST002 Osteoporosis 79 0.155
97
P ESP024 Esophagitis 62 0.155
98
HRW001 Hair Whorl 36 0.154
99
P ATS364 Autism 68 0.153
100
SKN016 Skin Disease 64 0.153
101
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.152
102
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.152
103
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.152
104
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.152
105
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.152
106
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.152
107
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.152
108
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.152
109
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.152
110
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.152
111
BRN071 Brain Injury 51 0.151
112
THR024 Thrombosis 58 0.151
113
PLM001 Pulmonary Tuberculosis 72 0.150
114
AST005 Asthma 80 0.149
115
P GLM007 Glomerulonephritis 58 0.149
116
PLM010 Pulmonary Edema 56 0.149
117
P PNC035 Pancreatic Cancer 86 0.149
118
c FTL070 Fetal Akinesia Deformation Sequence 2 33 0.148
119
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.148
120
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.148
121
CRB004 Cerebral Artery Occlusion 38 0.148
122
c ATS007 Autism Spectrum Disorder 69 0.147
123
PHN003 Phenylketonuria 73 0.147
124
STR067 Stroke, Ischemic 82 0.147
125
ANX004 Anoxia 44 0.146
126
BRN004 Brain Edema 57 0.146
127
P THR014 Thrombocytopenia 67 0.146
128
P GST044 Gastritis 58 0.145
129
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.145
130
c DNT047 Dentinogenesis Imperfecta Type 2 34 0.144
131
PPL052 Papillomatosis, Confluent and Reticulated 34 0.144
132
NNL006 Non-Alcoholic Steatohepatitis 53 0.143
133
P PLM037 Pulmonary Hypertension 69 0.143
134
P SCH015 Schizophrenia 76 0.143
135
STT001 Status Epilepticus 61 0.142
136
c ACT071 Acute Kidney Failure 60 0.142
137
P RHM011 Rheumatoid Arthritis 82 0.142
138
DPR016 Depression 64 0.140
139
NTR005 Nutritional Deficiency Disease 61 0.140
140
ALC007 Alcohol Dependence 68 0.139
141
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.139
142
AGN016 Aging 58 0.138
143
IRN002 Iron Metabolism Disease 58 0.137
144
MYL069 Myeloma, Multiple 85 0.136
145
PRT036 Peritonitis 66 0.136
146
SPN186 Spinal Cord Injury 63 0.135
147
CLF027 Cleft Palate, Isolated 67 0.135
148
TRM010 Traumatic Brain Injury 54 0.135
149
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.135
150
CNG034 Congestive Heart Failure 69 0.135
151
OCL069 Ocular Motor Apraxia 53 0.135
152
P BLD134 Bladder Cancer 79 0.134
153
TXC005 Toxic Shock Syndrome 63 0.134
154
CLN015 Colon Adenocarcinoma 65 0.133
155
URM002 Uremia 50 0.133
156
BRN024 Bronchitis 70 0.133
157
P RHN004 Rhinitis 59 0.132
158
BND020 Bone Disease 60 0.132
159
P ART022 Arthritis 71 0.132
160
P NRP001 Neuropathy 57 0.131
161
MNT002 Mental Depression 60 0.130
162
ADR007 Adrenoleukodystrophy 72 0.130
163
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.130
164
GST023 Gastric Ulcer 53 0.129
165
P NTR004 Neutropenia 64 0.129
166
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.129
167
P ART021 Arteriosclerosis 56 0.129
168
c HPT073 Hepatitis C Virus 74 0.128
169
ADR022 Adrenomyeloneuropathy 39 0.128
170
c MCR120 Microvascular Complications of Diabetes 7 48 0.127
171
c MCR113 Microvascular Complications of Diabetes 3 55 0.127
172
c RHB024 Rhabdomyosarcoma 2 64 0.127
173
c MGR028 Migraine with or Without Aura 1 70 0.127
174
c MCR130 Microvascular Complications of Diabetes 6 42 0.126
175
c MCR133 Microvascular Complications of Diabetes 4 42 0.126
176
c ACT027 Acute Pancreatitis 60 0.126
177
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.126
178
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.125
179
P LYM031 Lymphocytic Leukemia 56 0.124
180
P LTR001 Lateral Sclerosis 56 0.124
181
P HYP086 Hypothyroidism 70 0.124
182
P HRP006 Herpes Simplex 66 0.123
183
TTN003 Tetanus 62 0.123
184
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.123
185
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.123
186
OTT002 Otitis Media 71 0.122
187
INS001 Insulinoma 60 0.122
188
P GST053 Gastric Cancer 85 0.121
189
ANG054 Angina Pectoris 66 0.121
190
P PRD008 Periodontitis 66 0.120
191
MLN008 Melanoma 68 0.120
192
P AST007 Astrocytoma 52 0.120
193
P MYP004 Myopathy 63 0.119
194
SVR004 Severe Combined Immunodeficiency 74 0.119
195
PLM033 Pulmonary Embolism 60 0.118
196
BCT022 Bacterial Infectious Disease 57 0.118
197
ALL003 Allergic Rhinitis 69 0.118
198
IMM167 Immune Deficiency Disease 79 0.118
199
P HYP098 Hypereosinophilic Syndrome 67 0.116
200
P MJR001 Major Depressive Disorder 69 0.116
201
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.116
202
BRR014 Barrett Esophagus 67 0.115
203
c SYS001 Systemic Lupus Erythematosus 88 0.115
204
CNT047 Contact Dermatitis 58 0.115
205
SRC014 Sarcoma 67 0.114
206
SPN035 Spindle Cell Sarcoma 57 0.114
207
INT007 Intermediate Coronary Syndrome 58 0.114
208
PPL022 Papilloma 56 0.113
209
P NPH012 Nephrotic Syndrome 65 0.113
210
P RTN024 Retinoblastoma 74 0.110
211
c FML008 Familial Retinoblastoma 46 0.110
212
P MCR115 Microvascular Complications of Diabetes 5 67 0.110
213
SQM002 Squamous Cell Papilloma 49 0.109
214
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.109
215
P MSC005 Muscular Dystrophy 68 0.109
216
P RSP003 Respiratory Failure 75 0.108
217
PRS045 Prostatic Hypertrophy 55 0.107
218
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.107
219
P ALC033 Alcohol Use Disorder 58 0.107
220
RCK004 Rickets 70 0.107
221
P ECL001 Eclampsia 53 0.107
222
DBT010 Diabetic Neuropathy 56 0.106
223
P HDC001 Headache 59 0.106
224
ACQ007 Acquired Immunodeficiency Syndrome 61 0.106
225
P PNM007 Pneumonia 71 0.106
226
VCC001 Vaccinia 50 0.106
227
PRP027 Peripheral Vascular Disease 72 0.106
228
MST004 Mast Cell Neoplasm 40 0.105
229
EXT007 Extracutaneous Mastocytoma 39 0.105
230
PRX001 Peroxisomal Disease 45 0.104
231
c THR092 Thrombophilia Due to Thrombin Defect 74 0.104
232
ESP021 Esophageal Cancer 90 0.104
233
P PRP019 Peripheral Nervous System Disease 64 0.104
234
P CRD132 Cardiac Conduction Defect 61 0.104
235
c INH020 Inherited Metabolic Disorder 51 0.103
236
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.103
237
P HYP076 Hyperthyroidism 55 0.103
238
MSL001 Measles 61 0.103
239
P MLT020 Multiple Sclerosis 73 0.103
240
P SKN015 Skin Carcinoma 67 0.103
241
P LNG064 Lung Cancer Susceptibility 3 79 0.103
242
c DWL002 Dowling-Degos Disease 1 59 0.103
243
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.102
244
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.102
245
GST033 Gestational Diabetes 58 0.102
246
P CRD119 Cardiac Arrest 71 0.102
247
P LPS004 Lupus Erythematosus 62 0.102
248
THY029 Thyroid Carcinoma 62 0.101
249
P PRP029 Porphyria 58 0.101
250
ALL014 Allergic Encephalomyelitis 40 0.101
251
P ZLL001 Zellweger Syndrome 56 0.101
252
PTT037 Pituitary Tumors 47 0.101
253
CLR108 Colorectal Adenoma 64 0.100
254
PLY150 Polykaryocytosis Inducer 31 0.100
255
c HPT001 Hepatitis C 62 0.100
256
P INF038 Influenza 69 0.100
257
P ART023 Arthropathy 61 0.100
258
P PNC044 Pancreatitis 61 0.100
259
MDD011 Mood Disorder 62 0.099
260
P UVT001 Uveitis 58 0.098
261
PRS021 Prostatic Adenoma 52 0.098
262
RHM027 Rheumatic Disease 56 0.098
263
CHR074 Choriocarcinoma 47 0.098
264
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.097
265
CHL004 Cholelithiasis 50 0.097
266
IGR001 Ige Responsiveness, Atopic 61 0.097
267
PNG002 Pain Agnosia 52 0.097
268
KRT002 Keratomalacia 47 0.096
269
ERY051 Erythroleukemia, Familial 58 0.096
270
c ATR087 Atrial Standstill 1 76 0.096
271
PRS129 Prostatic Hyperplasia, Benign 49 0.096
272
P ADL010 Adult Respiratory Distress Syndrome 61 0.096
273
SCH014 Schistosomiasis 57 0.095
274
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 40 0.095
275
PRP030 Purpura 56 0.095
276
P ATR011 Atrial Fibrillation 67 0.095
277
c VRL010 Viral Hepatitis 56 0.095
278
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.094
279
c EXD008 Exudative Vitreoretinopathy 1 69 0.094
280
c LKM063 Leukemia, Chronic Myeloid 74 0.094
281
P INF032 Infertility 60 0.094
282
c LRG017 Large Intestine Cancer 53 0.094
283
P URT039 Urticaria 61 0.093
284
P ALP008 Alopecia 58 0.093
285
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 36 0.093
286
P PLY019 Polyneuropathy 55 0.092
287
ORL011 Oral Cancer 62 0.092
288
ENT011 Enterocolitis 51 0.092
289
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.092
290
TRN015 Transient Cerebral Ischemia 62 0.092
291
P SRC025 Sarcoidosis 1 72 0.091
292
EYD002 Eye Disease 59 0.091
293
SPP010 Suppressor of Tumorigenicity 3 54 0.091
294
CHL079 Children's Interstitial Lung Disease 27 0.091
295
RTN023 Retinitis 46 0.091
296
NRR001 Neuroretinitis 46 0.091
297
P MLN007 Male Infertility 57 0.091
298
MST005 Mastitis 55 0.090
299
RNL077 Renal Fibrosis 49 0.090
300
MSC007 Muscle Hypertrophy 65 0.090
301
c HPT016 Hepatitis B 63 0.090
302
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.090
303
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.089
304
PRT013 Portal Hypertension 61 0.089
305
P RTN008 Retinitis Pigmentosa 77 0.088
306
P PRK057 Parkinson Disease, Late-Onset 77 0.088
307
P DMN002 Dementia 68 0.088
308
PLR008 Pleurisy 50 0.088
309
P NMN002 Niemann-Pick Disease 60 0.088
310
ORL015 Oral Squamous Cell Carcinoma 44 0.087
311
ENT004 Enthesopathy 46 0.086
312
URT010 Ureteral Obstruction 46 0.086
313
c FML021 Familial Hypercholesterolemia 67 0.086
314
P PLM036 Pulmonary Fibrosis 66 0.086
315
IDP011 Idiopathic Interstitial Pneumonia 65 0.086
316
ARG004 Argyria 28 0.085
317
P TCL004 T-Cell Leukemia 48 0.085
318
c LKM005 Leukemia, T-Cell, Chronic 35 0.085
319
LPT014 Leptin Deficiency or Dysfunction 72 0.084
320
c LKM071 Leukemia, Chronic Lymphocytic 81 0.084
321
GTR002 Goiter 54 0.083
322
CRC021 Carcinosarcoma 62 0.083
323
PSY004 Psychotic Disorder 68 0.083
324
P SCK005 Sickle Cell Disease 53 0.083
325
P VSC011 Vasculitis 64 0.083
326
DSS009 Disseminated Intravascular Coagulation 58 0.082
327
END040 Endogenous Depression 55 0.082
328
ATS010 Autosomal Recessive Disease 49 0.082
329
ASP030 Aspirin Resistance 42 0.082
330
PRP080 Peripheral Artery Disease 51 0.082
331
P AMY004 Amyloidosis 71 0.082
332
LSH001 Leishmaniasis 64 0.082
333
P OBS001 Obstructive Jaundice 49 0.082
334
P KLZ004 Kala-Azar 1 43 0.082
335
c LKM004 Leukemia, B-Cell, Chronic 35 0.081
336
P RTN018 Retinal Disease 53 0.081
337
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.081
338
P RTN016 Retinal Degeneration 56 0.081
340
CRT015 Carotid Artery Occlusion 44 0.080
341
BRN028 Brain Cancer 75 0.080
342
END057 Endometrial Cancer 74 0.080
343
ALL006 Allergic Asthma 56 0.079
344
P DNG005 Dengue Virus 57 0.079
345
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.079
346
HDN002 Head Injury 47 0.079
347
NTR046 Neutrophil Migration 49 0.078
348
HMS001 Hemosiderosis 54 0.078
349
MSC157 Muscular Dystrophy, Duchenne Type 70 0.078
350
P CND004 Candidiasis 61 0.078
351
ALL010 Allergic Contact Dermatitis 56 0.077
352
P FML011 Familial Adenomatous Polyposis 73 0.077
353
P RCT021 Rectum Cancer 54 0.077
354
P RRH023 Rare Hereditary Hemochromatosis 41 0.076
355
KPS004 Kaposi Sarcoma 75 0.076
356
P SYS005 Systemic Scleroderma 68 0.076
357
P END044 Endometriosis 63 0.076
358
P PLY018 Polycythemia 56 0.075
359
ANR040 Aneurysm 60 0.075
360
ACR006 Aceruloplasminemia 74 0.075
361
YLL002 Yellow Fever 58 0.075
362
P INT068 Intestinal Disease 56 0.075
363
PRN019 Perinatal Necrotizing Enterocolitis 55 0.075
364
TXC020 Toxic Oil Syndrome 34 0.075
365
P MYC008 Myocarditis 60 0.075
366
RTN017 Retinal Detachment 62 0.074
367
CHG001 Chagas Disease 66 0.074
368
c DLT002 Dilated Cardiomyopathy 81 0.073
369
P SHR001 Short Bowel Syndrome 50 0.073
370
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.073
371
HPT022 Hepatoblastoma 58 0.073
372
HPT014 Hepatorenal Syndrome 49 0.072
373
P HML002 Hemolytic Anemia 64 0.072
374
PRT038 Protein-Energy Malnutrition 56 0.072
375
HYD002 Hydronephrosis 58 0.072
376
CHL067 Cholecystitis 60 0.072
377
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.072
378
c PRM038 Primary Agammaglobulinemia 45 0.071
379
KRT019 Keratitis, Hereditary 69 0.071
380
IMP005 Impotence 53 0.071
381
P HYD006 Hydrocephalus 68 0.070
382
c CNG216 Congenital Hydrocephalus 55 0.070
383
THY030 Thyroid Gland Disease 53 0.070
384
P PLY014 Polycystic Kidney Disease 61 0.070
385
CRB037 Cerebral Palsy 69 0.070
386
P HML001 Hemolytic-Uremic Syndrome 54 0.070
387
P CHR012 Chronic Granulomatous Disease 69 0.069
388
MNN042 Meningioma, Radiation-Induced 64 0.069
389
CRN027 Corneal Neovascularization 48 0.069
390
c PSR017 Psoriasis 2 55 0.069
391
c PSR023 Psoriasis 1 50 0.069
392
c PSR028 Psoriasis 7 40 0.069
393
c PSR018 Psoriasis 13 40 0.069
394
c PSR032 Psoriasis 11 40 0.069
395
c HYP555 Hypertriglyceridemia, Transient Infantile 38 0.069
396
VRL011 Viral Infectious Disease 62 0.068
397
IRR003 Irritant Dermatitis 46 0.068
398
MCL006 Macular Retinal Edema 52 0.068
399
VTR007 Vitreoretinopathy 48 0.068
400
P MNC007 Monocytic Leukemia 52 0.068
401
c HNT004 Huntington Disease-Like 2 48 0.068
402
c HNT011 Huntington Disease-Like 3 37 0.068
403
CRH005 Crohn's Colitis 56 0.067
404
MNT001 Mantle Cell Lymphoma 69 0.067
405
P RHB003 Rhabdomyosarcoma 62 0.067
406
P RNL015 Renal Hypertension 47 0.067
407
ART016 Aortic Aneurysm 71 0.067
408
BRN056 Bronchopulmonary Dysplasia 57 0.067
409
P MJR007 Major Affective Disorder 1 44 0.067
410
OST017 Osteomyelitis 65 0.066
411
VSC002 Vascular Dementia 57 0.066
412
CLR109 Colorectal Adenocarcinoma 51 0.066
413
PLY001 Polycythemia Vera 70 0.066
414
SDD001 Sudden Infant Death Syndrome 61 0.066
415
CRN017 Coronary Thrombosis 45 0.065
416
MLK006 Milk Allergy 44 0.065
417
ACT003 Acute Kidney Tubular Necrosis 42 0.065
418
SCK003 Sickle Cell Anemia 74 0.065
419
LYM027 Lymphopenia 58 0.065
420
HND015 Hand Skill, Relative 33 0.064
421
P THY023 Thymoma 64 0.064
422
P MMP001 Mumps 57 0.064
423
c THY107 Thymoma, Familial 55 0.064
424
PLS011 Plasmacytoma 57 0.064
425
CHR100 Chronic Ulcer of Skin 53 0.064
426
c FML001 Familial Atrial Fibrillation 67 0.063
427
P RBL001 Rubella 56 0.063
428
THR004 Thrombocytosis 52 0.063
429
P ICH004 Ichthyosis 55 0.062
430
P RHZ001 Rhizomelic Chondrodysplasia Punctata 53 0.062
431
WLL004 Wallerian Degeneration 40 0.062
432
P GRV001 Graves' Disease 57 0.062
433
CRN030 Coronary Stenosis 49 0.062
434
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 52 0.062
435
GRN017 Granulocytopenia 46 0.062
436
c SCN036 Secondary Progressive Multiple Sclerosis 54 0.062
437
VTR013 Vitreoretinopathy, Neovascular Inflammatory 61 0.061
438
CRT013 Carotid Stenosis 50 0.061
439
P END046 Endometritis 49 0.061
440
SLC006 Silicosis 55 0.061
441
SCH012 Schizoaffective Disorder 50 0.061
442
P CHN044 Chondrodysplasia Punctata Syndrome 42 0.061
443
CRD223 Cardiac Arrhythmia 61 0.059
444
INT002 Intermittent Claudication 60 0.059
446
c PLM127 Pulmonary Hypertension, Primary, 3 33 0.059
447
ENC005 Encephalomalacia 37 0.059
448
PLC006 Placental Choriocarcinoma 33 0.059
449
P THY032 Thyroiditis 52 0.059
450
P MMB011 Membranous Nephropathy 54 0.059
451
P ESS003 Essential Thrombocythemia 69 0.058
452
CYT008 Cytomegalovirus Infection 58 0.058
453
PLC005 Placental Insufficiency 55 0.058
454
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.057
455
SCH003 Schizophreniform Disorder 49 0.057
456
P LRY044 Larynx Cancer 59 0.057
457
ALC006 Alcoholic Hepatitis 60 0.057
458
CYN002 Cyanosis, Transient Neonatal 45 0.057
459
P TBR001 Tuberous Sclerosis 72 0.056
460
c BLD154 Bleeding Disorder, Platelet-Type, 12 28 0.056
461
P GLM044 Glomerular Disease 42 0.056
462
ART006 Arthus Reaction 43 0.056
463
PYR016 Pyridoxine Deficiency 31 0.055
464
NRN004 Neuroendocrine Tumor 59 0.055
465
PRX085 Preaxial Hallucal Polydactyly 27 0.055
466
c JVN010 Juvenile Rheumatoid Arthritis 67 0.055
467
RTC005 Reticulosarcoma 48 0.055
468
KWS002 Kawasaki Disease 65 0.054
469
P MRC003 Mercury Poisoning 47 0.054
470
P SNS001 Sensorineural Hearing Loss 62 0.054
471
THR100 Thrombocytopenic Purpura, Autoimmune 61 0.054
472
LST001 Listeriosis 55 0.054
473
c PRG019 Paragangliomas 2 30 0.054
474
BRN002 Bronchiolitis 60 0.053
475
P GLL020 Gallbladder Disease 60 0.053
476
P GNT008 Giant Cell Tumor 45 0.053
477
MYL031 Myeloproliferative Neoplasm 66 0.053
478
P OCL013 Oculodentodigital Dysplasia 65 0.053
479
c ART138 Aortic Aneurysm, Familial Abdominal, 1 62 0.053
480
c THY109 Thyroid Cancer, Nonmedullary, 1 58 0.053
481
P PTS002 Ptosis 53 0.053
482
ANR004 Anuria 47 0.053
483
TBC004 Tobacco Addiction 65 0.053
484
CRN019 Coronary Artery Vasospasm 48 0.053
485
P MCR010 Microcephaly 56 0.053
486
GNT167 Genetic Obesity 35 0.052
487
MYL005 Myelofibrosis 69 0.052
488
P PRV006 Pervasive Developmental Disorder 58 0.052
489
LMB062 Limb Ischemia 50 0.052
490
INT017 Intestinal Schistosomiasis 49 0.052
491
PPL049 Papillon-Lefevre Syndrome 63 0.051
492
P HMR003 Hemorrhagic Disease 54 0.051
493
LRN003 Learning Disability 51 0.051
494
PRV004 Periventricular Leukomalacia 50 0.051
495
SPP008 Suppurative Otitis Media 46 0.051
496
URN010 Urinary Tract Obstruction 59 0.051
497
P DRM010 Dermatomyositis 62 0.050
498
c FTL071 Fetal Akinesia Deformation Sequence 3 23 0.050
499
NRF026 Neurofibromatosis, Type Iv, of Riccardi 65 0.050
500
P APL001 Aplastic Anemia 76 0.049
501
P PRP003 Porphyria Cutanea Tarda 66 0.049
502
INT066 Interstitial Lung Disease 61 0.049
503
P LYD001 Leydig Cell Tumor 45 0.049
504
c WLM013 Wilms Tumor 1 69 0.049
505
c NMN015 Niemann-Pick Disease, Type C1 67 0.049
506
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.049
507
CRB090 Cerebral Hypoxia 45 0.049
508
ASP004 Asphyxia Neonatorum 44 0.049
509
c TBR025 Tuberous Sclerosis 1 74 0.048
510
P DBT005 Diabetes Insipidus 54 0.048
512
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 29 0.048
513
ATM052 Autoimmune Disease 1 38 0.048
514
TST014 Testicular Cancer 49 0.047
515
BRN014 Bronchopneumonia 47 0.047
516
INT052 Intestinal Volvulus 44 0.047
517
CNN001 Cannabis Dependence 41 0.047
518
CNN002 Cannabis Abuse 40 0.047
519
P PLY041 Polymyositis 57 0.047
520
CHK001 Chikungunya 55 0.047
521
LWC001 Low Compliance Bladder 45 0.047
522
ART002 Arts Syndrome 63 0.046
523
BLL006 Bullous Pemphigoid 63 0.046
524
c BCT013 Bacterial Pneumonia 49 0.045
525
PRS042 Prostate Disease 42 0.045
526
MST020 Mast Cell Activation Syndrome 28 0.045
527
INT078 Intracranial Thrombosis 48 0.045
528
P CLS010 Cluster Headache 44 0.045
529
c ATS013 Autosomal Recessive Congenital Ichthyosis 65 0.045
530
GLL018 Gallbladder Cancer 57 0.045
531
INT030 Intracranial Aneurysm 57 0.045
532
THY124 Thyroid Gland Papillary Carcinoma 54 0.045
533
GLC036 Glucagonoma 45 0.045
534
c HMG029 Hemoglobin Se Disease 40 0.045
535
SPR126 Superior Semicircular Canal Dehiscence 39 0.045
536
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.045
537
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 51 0.044
538
P BLD051 Blood Coagulation Disease 48 0.044
539
P FML187 Familial Hypertension 35 0.044
540
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 63 0.044
541
CRV038 Cervical Squamous Cell Carcinoma 58 0.044
542
ACH005 Achalasia 50 0.044
543
c ANT034 Anterior Uveitis 48 0.044
544
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.044
545
GNT029 Genetic Hypertension 39 0.044
546
c RTN047 Retinitis Pigmentosa 18 40 0.043
547
FLR002 Filariasis 56 0.043
548
c ACT020 Acute T Cell Leukemia 54 0.043
549
c SPR086 Spermatogenic Failure 3 41 0.043
550
SHW001 Shwartzman Phenomenon 35 0.042
551
ART031 Aortic Coarctation 45 0.042
552
PST010 Pasteurellosis 37 0.042
553
KSH001 Keshan Disease 36 0.042
554
IMM162 Immunoglobulin E Concentration, Serum 29 0.042
555
GLN010 Glanzmann Thrombasthenia 66 0.041
556
LYM017 Lyme Disease 64 0.041
557
P THR005 Thrombotic Thrombocytopenic Purpura 59 0.041
558
PLM012 Pulmonary Sarcoidosis 54 0.041
559
SPS003 Spastic Diplegia 53 0.041
560
NRN001 Neuroendocrine Carcinoma 48 0.041
561
ANT018 Anthracosis 46 0.041
562
DSS012 Disseminated Infection with Mycobacterium Avium Complex 21 0.041
563
P FML018 Familial Mediterranean Fever 70 0.041
564
CMM004 Common Variable Immunodeficiency 69 0.041
565
DBT008 Diabetic Angiopathy 42 0.041
566
MRP001 Morphine Dependence 41 0.041
567
MRF001 Marfan Syndrome 75 0.040
568
P PNM006 Pneumoconiosis 55 0.040
569
ESP023 Esophageal Disease 55 0.040
570
CHR005 Chorioamnionitis 51 0.040
571
c PRG020 Paragangliomas 3 36 0.040
572
RSP006 Respiratory System Disease 57 0.039
573
DRG003 Drug Dependence 48 0.039
574
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.039
575
LKS001 Leukostasis 43 0.039
576
P CRN024 Corneal Disease 42 0.039
577
LCH001 Leech Infestation 40 0.039
578
P WSK001 Wiskott-Aldrich Syndrome 71 0.039
579
SCH038 Schopf-Schulz-Passarge Syndrome 48 0.039
580
ART008 Arteriosclerosis Obliterans 40 0.039
581
MLD010 Mild Phenylketonuria 29 0.039
582
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 48 0.038
583
CRB008 Cerebral Atherosclerosis 47 0.038
584
BCT021 Bacterial Sepsis 44 0.038
585
CWP001 Cowpox 45 0.037
586
BYS001 Byssinosis 34 0.036
587
GRG001 Greig Cephalopolysyndactyly Syndrome 61 0.036
588
P BRT004 Bartter Disease 56 0.036
589
NPH010 Nephrosclerosis 46 0.036
590
P HRD144 Hereditary Mixed Polyposis Syndrome 38 0.036
591
STH001 Saethre-Chotzen Syndrome 66 0.035
592
PRC002 Paracoccidioidomycosis 55 0.035
593
P ACT105 Acute Mountain Sickness 53 0.035
594
P PLM006 Pulmonary Alveolar Proteinosis 50 0.035
595
ONC002 Onchocerciasis 50 0.035
596
EMB002 Embryoma 45 0.035
597
ACT162 Acute Sensory Ataxic Neuropathy 27 0.035
598
GRN037 Granulomatosis with Polyangiitis 62 0.034
599
HST011 Histoplasmosis 52 0.034
600
ALP048 Alopecia Totalis 31 0.034
601
THY006 Thymus Lymphoma 19 0.034
602
IMM001 Immune-Complex Glomerulonephritis 40 0.033
603
THY020 Thyroid Hyalinizing Trabecular Adenoma 23 0.033
604
BRN015 Bronchiolo-Alveolar Adenocarcinoma 56 0.032
605
OST006 Osteoblastoma 40 0.032
606
PNC005 Penicilliosis 40 0.032
607
ESP025 Esophagus Adenocarcinoma 39 0.032
608
c CHL142 Cholestasis, Intrahepatic, of Pregnancy 3 36 0.032
609
TQP001 Taqi Polymorphism 34 0.032
610
HYP855 Hyperpigmentation of the Skin 29 0.032
611
P USH001 Usher Syndrome 58 0.031
612
P CRB045 Cerebellar Hypoplasia 53 0.031
613
IDP035 Idiopathic Achalasia 46 0.031
614
P EXD001 Exudative Vitreoretinopathy 56 0.029
615
PTT041 Pituitary Stalk Interruption Syndrome 50 0.029
616
MGS001 Megaesophagus 47 0.029
617
PLY052 Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, and Cataract 45 0.029
618
P VTL001 Vitelliform Macular Dystrophy 43 0.029
619
PLT015 Platelet Aggregation, Spontaneous 40 0.029
620
VLK001 Volkmann Contracture 22 0.029
621
GRY002 Gray Platelet Syndrome 59 0.028
622
MLT134 Multiple Pterygium Syndrome, Lethal Type 50 0.028
623
NPH013 Nephrogenic Syndrome of Inappropriate Antidiuresis 36 0.028
624
SPR006 Sparganosis 34 0.028
625
c INF087 Inflammatory Bowel Disease 4 31 0.028
626
TRP021 Trpv4-Associated Disorders 13 0.028
627
QBC001 Quebec Platelet Disorder 39 0.026
628
LNG037 Lung Sarcoma 35 0.026
629
PRX009 Paroxysmal Hemicrania 33 0.026
630
GHS005 Ghosal Hematodiaphyseal Dysplasia 31 0.026
631
c BLD156 Bleeding Disorder, Platelet-Type, 14 29 0.026
632
c MNT287 Mental Retardation, Autosomal Recessive 57 24 0.026
633
c BLD123 Bleeding Disorder, Platelet-Type, 13 22 0.026
634
GST057 Gastro-Enteropancreatic Neuroendocrine Tumor 18 0.026
635
LKT001 Leukotriene C4 Synthase Deficiency 15 0.026
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