Search results for arachidonic acid

644 hits were found for arachidonic acid

# Family MCID Name MIFTS Score
1
PRT037 Pertussis 65 0.361
2
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.360
3
P LVR013 Liver Disease 68 0.301
4
FTT001 Fatty Liver Disease 61 0.295
5
P NRB001 Neuroblastoma 72 0.291
6
P CLR023 Colorectal Cancer 99 0.282
7
P GLM045 Glioma 63 0.262
8
GLL048 Glial Tumor 45 0.259
9
ISC004 Ischemia 58 0.255
10
LVR012 Liver Cirrhosis 62 0.252
11
P PSR002 Psoriasis 62 0.241
12
P BPL003 Bipolar Disorder 56 0.240
13
c MJR024 Major Affective Disorder 9 41 0.239
14
c MJR022 Major Affective Disorder 8 38 0.239
15
48X005 48,xyyy 39 0.238
16
PST011 Pustulosis of Palm and Sole 52 0.236
17
P PRS040 Prostate Cancer 97 0.235
18
P KDN018 Kidney Disease 72 0.233
19
P CRN300 Coronary Heart Disease 1 63 0.228
20
BNR002 Bone Resorption Disease 48 0.226
21
P INF037 Inflammatory Bowel Disease 54 0.225
22
LPD008 Lipid Metabolism Disorder 62 0.225
23
CHL068 Cholestasis 61 0.224
24
P BRS047 Breast Cancer 97 0.223
25
ATH013 Atherosclerosis Susceptibility 65 0.221
26
P DRR001 Diarrhea 55 0.218
27
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.214
28
P VSC007 Vascular Disease 63 0.211
29
ULC004 Ulcerative Colitis 73 0.211
30
c HYP836 Hypercholesterolemia, Familial, 1 73 0.210
31
P SZR006 Seizure Disorder 56 0.209
32
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.206
33
HYP066 Hyperglycemia 61 0.206
34
CLT003 Colitis 62 0.205
35
HLX001 Helix Syndrome 47 0.203
36
VSL002 Visual Epilepsy 59 0.203
37
CHL014 Cholera 59 0.203
38
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.203
39
NRL016 Neural Tube Defects 82 0.202
40
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.200
41
LPP008 Lipoprotein Quantitative Trait Locus 62 0.200
42
ALL026 Allergic Hypersensitivity Disease 62 0.199
43
OST012 Osteoarthritis 78 0.194
44
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.194
45
MTB004 Metabolic Acidosis 50 0.193
46
CYS001 Cystic Fibrosis 81 0.191
47
DRM006 Dermatitis 61 0.188
48
P HPT023 Hepatocellular Carcinoma 100 0.187
49
P ADN016 Adenocarcinoma 64 0.187
50
CYT002 Cytokine Deficiency 42 0.186
51
HYP266 Hypoxia 57 0.186
52
ART140 Arteries, Anomalies of 52 0.185
53
GST092 Gastroesophageal Reflux 67 0.185
54
c PRC016 Pre-Eclampsia 63 0.182
55
P DBT009 Diabetes Mellitus 64 0.182
56
P HYP750 Hypertriglyceridemia, Familial 62 0.181
57
GT001 Gout 64 0.181
58
c GLL024 Gallbladder Disease 1 53 0.179
59
HYP056 Hypoglycemia 66 0.179
60
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.178
61
P ENC018 Encephalopathy 61 0.176
62
P LKM002 Leukemia 68 0.176
63
P ALZ034 Alzheimer Disease 88 0.176
64
ADN018 Adenoma 59 0.170
65
P FBR017 Fibrosarcoma 56 0.168
66
ATM095 Autoimmune Disease 62 0.168
67
P HRT032 Heart Disease 75 0.167
68
HMN044 Human Immunodeficiency Virus Type 1 71 0.166
69
P MYL006 Myeloid Leukemia 60 0.165
70
c ACT075 Acute Myocardial Infarction 57 0.163
71
GLB015 Glioblastoma Multiforme 75 0.163
72
PPT005 Peptic Ulcer Disease 59 0.163
73
c PCH010 Pachyonychia Congenita 3 44 0.161
74
SQM006 Squamous Cell Carcinoma 60 0.161
75
OST159 Osteogenic Sarcoma 66 0.161
76
NNL006 Non-Alcoholic Steatohepatitis 54 0.160
77
P MYC007 Myocardial Infarction 70 0.160
78
P PHC003 Pheochromocytoma 71 0.159
79
HYP060 Hyperinsulinism 54 0.159
80
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.159
81
CRH001 Crohn's Disease 74 0.159
82
ADR040 Adrenal Gland Pheochromocytoma 46 0.159
83
P DRM053 Dermatitis, Atopic 66 0.156
84
P CRD246 Cardiovascular System Disease 57 0.153
85
DFC004 Deficiency Anemia 70 0.153
86
c HYP595 Hypertension, Essential 84 0.153
87
SKN016 Skin Disease 63 0.151
88
LNG099 Lung Disease 60 0.151
89
P ATS364 Autism 70 0.151
90
HRW001 Hair Whorl 36 0.150
91
P OVR042 Ovarian Cancer 88 0.150
92
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.150
93
P ESP024 Esophagitis 62 0.149
94
P OST002 Osteoporosis 74 0.149
95
P LNG032 Lung Cancer 98 0.149
96
P PNC035 Pancreatic Cancer 84 0.149
97
c ATS007 Autism Spectrum Disorder 67 0.149
98
CRB004 Cerebral Artery Occlusion 45 0.146
99
PLM010 Pulmonary Edema 54 0.145
100
PLM001 Pulmonary Tuberculosis 69 0.145
101
P GLM007 Glomerulonephritis 57 0.145
102
c CHR684 Chronic Kidney Disease 70 0.145
103
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.144
104
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.144
105
PHN003 Phenylketonuria 75 0.144
106
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.143
107
BRN004 Brain Edema 56 0.143
108
AST005 Asthma 76 0.142
109
ANX004 Anoxia 40 0.142
110
PPL052 Papillomatosis, Confluent and Reticulated 33 0.142
111
P GST044 Gastritis 56 0.141
112
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.140
113
STT001 Status Epilepticus 60 0.140
114
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.140
115
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.140
116
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.140
117
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.140
118
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.140
119
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.140
120
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.140
121
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.140
122
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.140
123
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.139
124
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.139
125
CRB039 Cerebrovascular Disease 67 0.139
126
BRN071 Brain Injury 49 0.138
127
NTR005 Nutritional Deficiency Disease 62 0.138
128
CNG034 Congestive Heart Failure 69 0.138
129
c ACT071 Acute Kidney Failure 60 0.138
130
STR067 Stroke, Ischemic 81 0.138
131
DPR016 Depression 63 0.137
132
47X002 47,xyy 49 0.136
133
TXC005 Toxic Shock Syndrome 62 0.136
134
P SCH015 Schizophrenia 74 0.135
135
P ART022 Arthritis 69 0.134
136
ALC007 Alcohol Dependence 66 0.134
137
P PLM037 Pulmonary Hypertension 67 0.134
138
P THR014 Thrombocytopenia 67 0.133
139
NPH009 Nephrolithiasis 55 0.133
140
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.133
141
IRN002 Iron Metabolism Disease 57 0.133
142
PRT036 Peritonitis 64 0.133
143
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.132
144
CLF027 Cleft Palate, Isolated 64 0.132
145
P RHM011 Rheumatoid Arthritis 80 0.131
146
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.130
147
P RHN004 Rhinitis 57 0.130
148
BRN024 Bronchitis 68 0.130
149
P BND020 Bone Disease 59 0.129
150
URM002 Uremia 49 0.129
151
MNT002 Mental Depression 58 0.128
152
OCL069 Ocular Motor Apraxia 51 0.128
153
P BLD134 Bladder Cancer 79 0.128
154
P NRP001 Neuropathy 56 0.127
155
CLN015 Colon Adenocarcinoma 65 0.127
156
GST023 Gastric Ulcer 53 0.126
157
c MCR120 Microvascular Complications of Diabetes 7 47 0.126
158
ADR007 Adrenoleukodystrophy 75 0.126
159
c ACT027 Acute Pancreatitis 60 0.126
160
c DBT099 Diabetes Mellitus, Type I 65 0.126
161
c MCR113 Microvascular Complications of Diabetes 3 52 0.126
162
TRM010 Traumatic Brain Injury 51 0.126
163
SPN186 Spinal Cord Injury 60 0.126
164
c MCR130 Microvascular Complications of Diabetes 6 41 0.125
165
c MCR133 Microvascular Complications of Diabetes 4 41 0.125
166
P ART021 Arteriosclerosis 54 0.125
167
P NTR004 Neutropenia 63 0.125
168
MYL069 Myeloma, Multiple 85 0.124
169
ADR022 Adrenomyeloneuropathy 38 0.123
170
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.123
171
c HPT073 Hepatitis C Virus 72 0.123
172
THR024 Thrombosis 57 0.122
173
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.122
174
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.122
175
P MLN008 Melanoma 69 0.121
176
P PRD008 Periodontitis 64 0.121
177
P LTR001 Lateral Sclerosis 54 0.121
178
AGN016 Aging 56 0.120
179
BCT022 Bacterial Infectious Disease 56 0.120
180
c MGR028 Migraine with or Without Aura 1 67 0.120
181
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.120
182
TTN003 Tetanus 65 0.120
183
c RHB024 Rhabdomyosarcoma 2 67 0.120
184
P HYP086 Hypothyroidism 69 0.120
185
INS001 Insulinoma 60 0.119
186
OTT002 Otitis Media 72 0.118
187
P HRP006 Herpes Simplex 65 0.118
188
ANG054 Angina Pectoris 66 0.117
189
P GST053 Gastric Cancer 83 0.117
190
P AST007 Astrocytoma 51 0.116
191
SVR004 Severe Combined Immunodeficiency 73 0.116
192
PLM033 Pulmonary Embolism 59 0.115
193
ALL003 Allergic Rhinitis 67 0.115
194
P MYP004 Myopathy 70 0.115
195
P MJR001 Major Depressive Disorder 68 0.115
196
CNT047 Contact Dermatitis 58 0.113
197
P HYP098 Hypereosinophilic Syndrome 67 0.113
198
c SYS001 Systemic Lupus Erythematosus 86 0.112
199
BRR014 Barrett Esophagus 65 0.112
200
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.112
201
RCK004 Rickets 68 0.111
202
INT007 Intermediate Coronary Syndrome 55 0.111
203
c THR092 Thrombophilia Due to Thrombin Defect 73 0.111
204
c LKM063 Leukemia, Chronic Myeloid 72 0.111
205
PPL022 Papilloma 54 0.110
206
P NPH012 Nephrotic Syndrome 60 0.109
207
P MCR115 Microvascular Complications of Diabetes 5 66 0.108
208
SRC014 Sarcoma 65 0.108
209
SPN035 Spindle Cell Sarcoma 53 0.108
210
SQM002 Squamous Cell Papilloma 46 0.107
211
P RTN024 Retinoblastoma 73 0.107
212
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.107
213
IMM167 Immune Deficiency Disease 78 0.107
214
c FML008 Familial Retinoblastoma 53 0.107
215
P RSP003 Respiratory Failure 74 0.106
216
P MSC005 Muscular Dystrophy 66 0.105
217
DBT010 Diabetic Neuropathy 54 0.105
218
P ECL001 Eclampsia 50 0.105
219
PRS045 Prostatic Hypertrophy 53 0.105
220
P PNM007 Pneumonia 68 0.104
221
GST033 Gestational Diabetes 61 0.104
222
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.103
223
P ALC033 Alcohol Use Disorder 58 0.103
224
c DWL002 Dowling-Degos Disease 1 58 0.103
225
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.103
226
PRP027 Peripheral Vascular Disease 71 0.103
227
P SKN015 Skin Carcinoma 66 0.102
228
P PRP019 Peripheral Nervous System Disease 58 0.102
229
VCC001 Vaccinia 49 0.102
230
MST004 Mast Cell Neoplasm 42 0.102
231
EXT007 Extracutaneous Mastocytoma 38 0.102
232
CRD132 Cardiac Conduction Defect 58 0.102
233
P LNG064 Lung Cancer Susceptibility 3 78 0.102
234
MSL001 Measles 62 0.101
235
P HDC001 Headache 57 0.101
236
ESP021 Esophageal Cancer 90 0.101
237
PRX001 Peroxisomal Disease 46 0.101
238
c INH020 Inherited Metabolic Disorder 47 0.100
239
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.100
240
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.100
241
P ADL010 Adult Respiratory Distress Syndrome 65 0.100
242
P HYP076 Hyperthyroidism 55 0.100
243
P ATR011 Atrial Fibrillation 66 0.099
244
THY029 Thyroid Carcinoma 59 0.099
245
ALL014 Allergic Encephalomyelitis 38 0.099
246
PTT037 Pituitary Tumors 44 0.098
247
P ART023 Arthropathy 62 0.098
248
P PRP029 Porphyria 62 0.098
249
PLY150 Polykaryocytosis Inducer 31 0.098
250
P CRD119 Cardiac Arrest 67 0.098
251
ACQ007 Acquired Immunodeficiency Syndrome 60 0.097
252
P ZLL001 Zellweger Syndrome 57 0.097
253
P LPS004 Lupus Erythematosus 61 0.097
254
CLR108 Colorectal Adenoma 64 0.097
255
MDD011 Mood Disorder 62 0.097
256
c HPT001 Hepatitis C 62 0.096
257
P UVT001 Uveitis 57 0.096
258
PRS021 Prostatic Adenoma 51 0.096
259
P PNC044 Pancreatitis 61 0.095
260
P PLM036 Pulmonary Fibrosis 65 0.095
261
CHR074 Choriocarcinoma 47 0.095
262
KRT002 Keratomalacia 47 0.094
263
IGR001 Ige Responsiveness, Atopic 59 0.094
264
PNG002 Pain Agnosia 51 0.094
265
CHL004 Cholelithiasis 49 0.094
266
SCH014 Schistosomiasis 57 0.094
267
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.094
268
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.093
269
ERY051 Erythroleukemia, Familial 56 0.093
270
PRS129 Prostatic Hyperplasia, Benign 49 0.093
271
PRP030 Purpura 54 0.093
272
c EXD008 Exudative Vitreoretinopathy 1 71 0.092
273
P INF038 Influenza 68 0.092
274
RNL077 Renal Fibrosis 47 0.092
275
P ALP008 Alopecia 54 0.091
276
c VRL010 Viral Hepatitis 52 0.091
277
EYD002 Eye Disease 58 0.091
278
ENT011 Enterocolitis 51 0.091
279
CNS004 Constipation 58 0.091
280
P URT039 Urticaria 58 0.091
281
P INF032 Infertility 57 0.091
282
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.091
283
P MLN007 Male Infertility 55 0.090
284
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.090
285
ORL011 Oral Cancer 60 0.090
286
P PLY019 Polyneuropathy 56 0.090
287
MST005 Mastitis 53 0.089
288
CHL079 Children's Interstitial Lung Disease 26 0.089
289
ATS010 Autosomal Recessive Disease 48 0.089
290
P SPP010 Suppressor of Tumorigenicity 3 51 0.089
291
c ATR087 Atrial Standstill 1 75 0.089
292
TRN015 Transient Cerebral Ischemia 63 0.088
293
MSC007 Muscle Hypertrophy 64 0.088
294
RTN023 Retinitis 46 0.088
295
NRR001 Neuroretinitis 42 0.088
296
ORL015 Oral Squamous Cell Carcinoma 43 0.087
297
P SRC025 Sarcoidosis 1 70 0.087
298
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.087
299
c HPT016 Hepatitis B 59 0.086
300
PRT013 Portal Hypertension 59 0.086
301
GST050 Gastrointestinal System Disease 56 0.086
302
P RTN008 Retinitis Pigmentosa 79 0.086
303
P NMN002 Niemann-Pick Disease 59 0.086
304
PLR008 Pleurisy 50 0.086
305
URT010 Ureteral Obstruction 45 0.085
306
P PRK057 Parkinson Disease, Late-Onset 78 0.085
307
ENT004 Enthesopathy 49 0.084
308
P PLY011 Polycystic Ovary Syndrome 56 0.084
309
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.084
310
P DMN002 Dementia 66 0.084
311
ARG004 Argyria 27 0.083
312
c LKM005 Leukemia, T-Cell, Chronic 34 0.083
313
LPT014 Leptin Deficiency or Dysfunction 74 0.083
314
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.082
315
P SCK005 Sickle Cell Disease 50 0.081
316
PSY004 Psychotic Disorder 67 0.081
317
ALL006 Allergic Asthma 56 0.081
318
LSH001 Leishmaniasis 63 0.081
319
P KLZ004 Kala-Azar 1 41 0.081
320
P MNC007 Monocytic Leukemia 53 0.081
321
GTR002 Goiter 53 0.081
322
P LKM071 Leukemia, Chronic Lymphocytic 79 0.081
323
P RTN018 Retinal Disease 53 0.081
324
CRC021 Carcinosarcoma 62 0.080
325
P AMY004 Amyloidosis 70 0.080
326
P VSC011 Vasculitis 62 0.080
327
PRP080 Peripheral Artery Disease 53 0.080
328
P GLM040 Glioma Susceptibility 1 81 0.080
329
P THL005 Thalassemia 60 0.080
330
P DNG005 Dengue Virus 59 0.080
331
DSS009 Disseminated Intravascular Coagulation 57 0.080
332
ASP030 Aspirin Resistance 39 0.080
333
P RTN016 Retinal Degeneration 53 0.080
334
P OBS001 Obstructive Jaundice 50 0.079
335
END040 Endogenous Depression 55 0.078
337
P HML002 Hemolytic Anemia 63 0.078
338
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.078
339
BRN028 Brain Cancer 74 0.078
340
END057 Endometrial Cancer 74 0.078
341
CRT015 Carotid Artery Occlusion 45 0.078
342
c FML021 Familial Hypercholesterolemia 66 0.078
343
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.078
344
P CND004 Candidiasis 58 0.077
345
HDN002 Head Injury 46 0.077
346
NTR046 Neutrophil Migration 50 0.077
347
HMS001 Hemosiderosis 54 0.077
348
P END044 Endometriosis 63 0.075
349
ALL010 Allergic Contact Dermatitis 56 0.075
350
MSC157 Muscular Dystrophy, Duchenne Type 72 0.075
351
P FML011 Familial Adenomatous Polyposis 72 0.075
352
P RRH023 Rare Hereditary Hemochromatosis 41 0.075
353
PRN019 Perinatal Necrotizing Enterocolitis 59 0.075
354
P SYS005 Systemic Scleroderma 68 0.075
355
P INT068 Intestinal Disease 53 0.075
356
P RCT021 Rectum Cancer 52 0.074
357
KPS004 Kaposi Sarcoma 75 0.074
358
RTN017 Retinal Detachment 61 0.073
359
YLL002 Yellow Fever 61 0.073
360
TXC020 Toxic Oil Syndrome 33 0.073
361
P MYC008 Myocarditis 59 0.073
362
P PLY018 Polycythemia 56 0.073
363
ANR040 Aneurysm 59 0.072
364
CHG001 Chagas Disease 66 0.072
365
c DLT002 Dilated Cardiomyopathy 79 0.071
366
P SHR001 Short Bowel Syndrome 53 0.071
367
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.071
368
HPT022 Hepatoblastoma 56 0.071
369
c PRM038 Primary Agammaglobulinemia 44 0.070
370
KRT019 Keratitis, Hereditary 65 0.070
371
VRL011 Viral Infectious Disease 61 0.070
372
c PNS012 Paine Syndrome 61 0.070
373
PRT038 Protein-Energy Malnutrition 54 0.070
374
HPT014 Hepatorenal Syndrome 50 0.070
375
HYD002 Hydronephrosis 60 0.070
376
P PLY014 Polycystic Kidney Disease 62 0.069
377
IMP005 Impotence 52 0.069
378
MNN042 Meningioma, Radiation-Induced 62 0.069
379
CRB037 Cerebral Palsy 69 0.069
380
CHL067 Cholecystitis 57 0.069
381
P HML001 Hemolytic-Uremic Syndrome 53 0.068
382
P HYD006 Hydrocephalus 66 0.068
383
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.068
384
THY030 Thyroid Gland Disease 52 0.068
385
CRN027 Corneal Neovascularization 47 0.068
386
ART016 Aortic Aneurysm 69 0.067
387
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.067
388
P VTR007 Vitreoretinopathy 46 0.067
389
P CHR012 Chronic Granulomatous Disease 67 0.067
390
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.067
391
ANR007 Anorexia Nervosa 63 0.067
392
MCL006 Macular Retinal Edema 55 0.066
393
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.066
394
IRR003 Irritant Dermatitis 49 0.066
395
SDD001 Sudden Infant Death Syndrome 61 0.066
396
BRN056 Bronchopulmonary Dysplasia 57 0.066
397
c PSR017 Psoriasis 2 53 0.066
398
c PSR023 Psoriasis 1 52 0.066
399
c PSR032 Psoriasis 11 47 0.066
400
c PSR028 Psoriasis 7 42 0.066
401
c PSR018 Psoriasis 13 41 0.066
402
P RHB003 Rhabdomyosarcoma 63 0.065
403
CLR109 Colorectal Adenocarcinoma 51 0.065
404
c HNT004 Huntington Disease-Like 2 50 0.065
405
c HNT011 Huntington Disease-Like 3 38 0.065
406
P RNL015 Renal Hypertension 47 0.065
407
VSC002 Vascular Dementia 57 0.065
408
CRH005 Crohn's Colitis 53 0.065
409
P MJR007 Major Affective Disorder 1 43 0.065
410
OST017 Osteomyelitis 64 0.064
411
CHR100 Chronic Ulcer of Skin 55 0.064
412
ACT003 Acute Kidney Tubular Necrosis 45 0.064
413
MLK006 Milk Allergy 48 0.064
414
MNT001 Mantle Cell Lymphoma 69 0.064
415
SCK003 Sickle Cell Anemia 74 0.064
416
LYM027 Lymphopenia 58 0.064
417
CRN017 Coronary Thrombosis 47 0.063
418
HND015 Hand Skill, Relative 33 0.063
419
P MMP001 Mumps 58 0.063
420
P THY023 Thymoma 65 0.062
421
c THY107 Thymoma, Familial 52 0.062
422
PLY001 Polycythemia Vera 69 0.062
423
c BTT014 Beta-Thalassemia 74 0.062
424
P ICH004 Ichthyosis 54 0.062
425
P RBL001 Rubella 59 0.062
426
CRN030 Coronary Stenosis 50 0.061
427
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.061
428
PLS011 Plasmacytoma 56 0.061
429
P END046 Endometritis 49 0.061
430
c FML001 Familial Atrial Fibrillation 65 0.060
431
P RHZ001 Rhizomelic Chondrodysplasia Punctata 53 0.060
432
THR004 Thrombocytosis 51 0.060
433
WLL004 Wallerian Degeneration 39 0.060
434
GRN017 Granulocytopenia 44 0.060
435
P GRV001 Graves' Disease 55 0.060
436
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.060
438
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.059
439
CRT013 Carotid Stenosis 50 0.059
440
SLC006 Silicosis 56 0.059
441
P CHN044 Chondrodysplasia Punctata Syndrome 43 0.059
442
CRD223 Cardiac Arrhythmia 60 0.059
443
SCH012 Schizoaffective Disorder 50 0.058
444
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.058
445
P MMB011 Membranous Nephropathy 50 0.058
446
ENC005 Encephalomalacia 43 0.058
447
INT002 Intermittent Claudication 61 0.057
448
P THY032 Thyroiditis 52 0.057
449
PLC006 Placental Choriocarcinoma 36 0.057
450
CYT008 Cytomegalovirus Infection 57 0.057
451
PLC005 Placental Insufficiency 57 0.057
452
ART006 Arthus Reaction 44 0.056
453
P TBR001 Tuberous Sclerosis 70 0.056
454
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.056
455
BRC012 Brucellosis 64 0.055
456
SCH003 Schizophreniform Disorder 56 0.055
457
CYN002 Cyanosis, Transient Neonatal 45 0.055
458
GLM044 Glomerular Disease 37 0.055
459
ALC006 Alcoholic Hepatitis 61 0.055
460
P LRY044 Larynx Cancer 55 0.055
461
c BLD154 Bleeding Disorder, Platelet-Type, 12 29 0.055
462
P ESS003 Essential Thrombocythemia 68 0.055
463
P MCR010 Microcephaly 59 0.054
464
NRN004 Neuroendocrine Tumor 55 0.054
465
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.054
466
LST001 Listeriosis 56 0.054
467
FNG017 Fungal Infectious Disease 53 0.054
468
PYR016 Pyridoxine Deficiency 30 0.054
469
PRX085 Preaxial Hallucal Polydactyly 28 0.053
470
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.053
471
BRN002 Bronchiolitis 59 0.053
472
P MRC003 Mercury Poisoning 48 0.053
473
c JVN010 Juvenile Rheumatoid Arthritis 64 0.053
474
c PRG019 Paragangliomas 2 31 0.052
475
P SNS001 Sensorineural Hearing Loss 60 0.052
476
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.052
477
KWS002 Kawasaki Disease 65 0.052
478
ANR004 Anuria 46 0.052
479
P GLL020 Gallbladder Disease 57 0.051
480
P PTS002 Ptosis 53 0.051
481
TBC004 Tobacco Addiction 64 0.051
482
CRN019 Coronary Artery Vasospasm 46 0.051
483
INT017 Intestinal Schistosomiasis 48 0.051
484
GNT167 Genetic Obesity 33 0.051
485
P OCL013 Oculodentodigital Dysplasia 69 0.051
486
PPL049 Papillon-Lefevre Syndrome 65 0.051
487
P PRV006 Pervasive Developmental Disorder 57 0.051
488
HYP080 Hypogonadism 50 0.051
489
P HMR003 Hemorrhagic Disease 53 0.050
490
LRN003 Learning Disability 49 0.050
491
c FTL071 Fetal Akinesia Deformation Sequence 3 28 0.050
492
URN010 Urinary Tract Obstruction 55 0.050
493
MYL031 Myeloproliferative Neoplasm 66 0.049
494
LMB062 Limb Ischemia 55 0.049
495
PRV004 Periventricular Leukomalacia 52 0.049
496
SPP008 Suppurative Otitis Media 45 0.049
497
MYL005 Myelofibrosis 70 0.049
498
INT066 Interstitial Lung Disease 60 0.049
499
P NRF002 Neurofibromatosis 56 0.049
500
c TBR025 Tuberous Sclerosis 1 77 0.048
501
c NMN015 Niemann-Pick Disease, Type C1 68 0.048
502
c ALP101 Alpha-Thalassemia 62 0.048
503
P PRP003 Porphyria Cutanea Tarda 67 0.048
504
P DRM010 Dermatomyositis 61 0.048
506
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.048
507
ATM052 Autoimmune Disease 1 37 0.048
508
LYD001 Leydig Cell Tumor 45 0.048
509
P DBT005 Diabetes Insipidus 55 0.047
510
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.047
511
MST020 Mast Cell Activation Syndrome 26 0.047
512
P APL001 Aplastic Anemia 74 0.047
513
c WLM013 Wilms Tumor 1 65 0.047
514
CHK001 Chikungunya 57 0.047
515
CRB090 Cerebral Hypoxia 44 0.047
516
LWC001 Low Compliance Bladder 43 0.047
517
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.047
518
INT078 Intracranial Thrombosis 49 0.046
519
INT030 Intracranial Aneurysm 56 0.046
520
BRN014 Bronchopneumonia 54 0.046
521
P THR015 Thrombophilia 51 0.046
522
VLV047 Volvulus of Midgut 49 0.046
523
RTC005 Reticulosarcoma 47 0.046
524
TST014 Testicular Cancer 46 0.046
525
ART002 Arts Syndrome 64 0.045
526
SPR126 Superior Semicircular Canal Dehiscence 40 0.045
527
c HMG029 Hemoglobin Se Disease 39 0.045
528
RSP006 Respiratory System Disease 50 0.045
529
BKR002 Baker-Gordon Syndrome 49 0.045
530
CNN002 Cannabis Abuse 44 0.045
531
P CLS010 Cluster Headache 42 0.045
532
CNN001 Cannabis Dependence 40 0.045
533
c JVN061 Juvenile Arthritis 60 0.045
534
P PLY041 Polymyositis 57 0.045
535
ASP004 Asphyxia Neonatorum 46 0.045
536
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.045
537
BLL006 Bullous Pemphigoid 62 0.044
538
P GLL018 Gallbladder Cancer 57 0.044
539
c BCT013 Bacterial Pneumonia 48 0.044
540
GLC036 Glucagonoma 45 0.044
541
PRS042 Prostate Disease 43 0.044
542
c RTN047 Retinitis Pigmentosa 18 42 0.044
543
IRD001 Iridocyclitis 53 0.044
544
P FML187 Familial Hypertension 37 0.044
545
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.043
546
c ATS013 Autosomal Recessive Congenital Ichthyosis 63 0.042
547
CRV038 Cervical Squamous Cell Carcinoma 58 0.042
548
BLD053 Blood Platelet Disease 49 0.042
549
P BLD051 Blood Coagulation Disease 46 0.042
550
P BNG095 Benign Giant Cell Tumor 44 0.042
551
c SPR086 Spermatogenic Failure 3 44 0.042
552
FLR002 Filariasis 55 0.041
553
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.041
554
GLN010 Glanzmann Thrombasthenia 66 0.041
555
c NMN014 Niemann-Pick Disease, Type C2 51 0.041
556
ACH005 Achalasia 51 0.041
557
SHW001 Shwartzman Phenomenon 37 0.041
558
KSH001 Keshan Disease 34 0.041
559
PST010 Pasteurellosis 34 0.041
560
IMM162 Immunoglobulin E Concentration, Serum 28 0.041
561
LYM017 Lyme Disease 64 0.040
562
CHR005 Chorioamnionitis 51 0.040
563
ANT018 Anthracosis 48 0.040
564
DSS012 Disseminated Infection with Mycobacterium Avium Complex 20 0.040
565
P FML018 Familial Mediterranean Fever 73 0.039
566
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.039
567
PLM012 Pulmonary Sarcoidosis 53 0.039
568
DBT008 Diabetic Angiopathy 44 0.039
569
P CRN024 Corneal Disease 44 0.039
570
MRP001 Morphine Dependence 41 0.039
571
MRF001 Marfan Syndrome 77 0.039
572
CMM004 Common Variable Immunodeficiency 68 0.039
573
P PNM006 Pneumoconiosis 56 0.039
574
ESP023 Esophageal Disease 52 0.039
575
SPS003 Spastic Diplegia 51 0.039
576
NRN001 Neuroendocrine Carcinoma 47 0.039
577
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.039
578
c PRG020 Paragangliomas 3 39 0.039
579
P PRG013 Paraganglioma 52 0.038
580
LCH001 Leech Infestation 35 0.038
581
SCH038 Schopf-Schulz-Passarge Syndrome 55 0.037
582
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 52 0.037
583
DRG003 Drug Dependence 47 0.037
584
LKS001 Leukostasis 46 0.037
585
CRB008 Cerebral Atherosclerosis 44 0.037
586
ART008 Arteriosclerosis Obliterans 40 0.037
587
P CRC039 Coarctation of Aorta 47 0.037
588
P WSK001 Wiskott-Aldrich Syndrome 72 0.037
589
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.037
590
BCT021 Bacterial Sepsis 44 0.037
591
HPR006 Heparin Cofactor Ii Deficiency 40 0.037
592
CWP001 Cowpox 46 0.036
593
BYS001 Byssinosis 28 0.035
594
P BRT004 Bartter Disease 52 0.035
595
P HRD144 Hereditary Mixed Polyposis Syndrome 51 0.035
596
NPH010 Nephrosclerosis 50 0.035
597
THY020 Thyroid Hyalinizing Trabecular Adenoma 21 0.035
598
STH001 Saethre-Chotzen Syndrome 67 0.034
599
GRG001 Greig Cephalopolysyndactyly Syndrome 66 0.034
600
PRC002 Paracoccidioidomycosis 54 0.034
601
P PLM006 Pulmonary Alveolar Proteinosis 53 0.034
602
P ACT105 Acute Mountain Sickness 52 0.034
603
ACT162 Acute Sensory Ataxic Neuropathy 26 0.034
604
HST011 Histoplasmosis 55 0.033
605
ONC002 Onchocerciasis 52 0.033
606
EMB002 Embryoma 38 0.033
607
ALP048 Alopecia Totalis 32 0.033
608
THY006 Thymus Lymphoma 26 0.033
609
GRN037 Granulomatosis with Polyangiitis 65 0.032
610
IMM001 Immune-Complex Glomerulonephritis 40 0.032
611
BRN015 Bronchiolo-Alveolar Adenocarcinoma 54 0.031
612
c CNG027 Congenital Hemolytic Anemia 50 0.031
613
HYP784 Hypogonadism, Male 40 0.031
614
c CHL142 Cholestasis, Intrahepatic, of Pregnancy 3 38 0.031
615
OST006 Osteoblastoma 38 0.031
616
TQP001 Taqi Polymorphism 32 0.031
617
HYP855 Hyperpigmentation of the Skin 27 0.031
618
P USH001 Usher Syndrome 60 0.030
619
P VTL001 Vitelliform Macular Dystrophy 42 0.030
620
CRD118 Cardiovascular Cancer 41 0.030
621
P CRB045 Cerebellar Hypoplasia 41 0.030
622
ESP025 Esophagus Adenocarcinoma 38 0.030
623
P PHC019 Pheochromocytoma-Paraganglioma 36 0.030
624
PNC005 Penicilliosis 34 0.030
625
P EXD001 Exudative Vitreoretinopathy 55 0.029
626
MLT134 Multiple Pterygium Syndrome, Lethal Type 51 0.029
627
PTT041 Pituitary Stalk Interruption Syndrome 50 0.029
628
PLY052 Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, and Cataract 44 0.029
629
MGS001 Megaesophagus 43 0.029
630
VLK001 Volkmann Contracture 25 0.029
631
GRY002 Gray Platelet Syndrome 59 0.027
632
NPH013 Nephrogenic Syndrome of Inappropriate Antidiuresis 36 0.027
633
SPR006 Sparganosis 34 0.027
634
c INF087 Inflammatory Bowel Disease 4 26 0.027
635
TRP021 Trpv4-Associated Disorders 13 0.027
636
QBC001 Quebec Platelet Disorder 43 0.025
637
PRX009 Paroxysmal Hemicrania 33 0.025
638
GHS005 Ghosal Hematodiaphyseal Dysplasia 33 0.025
639
LNG037 Lung Sarcoma 32 0.025
640
c BLD156 Bleeding Disorder, Platelet-Type, 14 32 0.025
641
c MNT287 Mental Retardation, Autosomal Recessive 57 22 0.025
642
c BLD123 Bleeding Disorder, Platelet-Type, 13 22 0.025
643
GST057 Gastro-Enteropancreatic Neuroendocrine Tumor 17 0.025
644
LKT001 Leukotriene C4 Synthase Deficiency 15 0.025
Content
Loading form....