Search results for linoleic acid

429 hits were found for linoleic acid

# Family MCID Name MIFTS Score
1
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.487
2
FTT001 Fatty Liver Disease 63 0.361
3
P CLR023 Colorectal Cancer 100 0.338
4
P LVR013 Liver Disease 71 0.318
5
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.306
6
PLM017 Pulmonary Alveolar Microlithiasis 54 0.301
7
ATH013 Atherosclerosis Susceptibility 68 0.291
8
P KDN018 Kidney Disease 73 0.280
9
P CRN300 Coronary Heart Disease 1 59 0.269
10
LPD008 Lipid Metabolism Disorder 64 0.266
11
P BRS047 Breast Cancer 99 0.260
12
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.259
13
c HYP836 Hypercholesterolemia, Familial, 1 74 0.259
14
LVR012 Liver Cirrhosis 67 0.255
15
BNR002 Bone Resorption Disease 51 0.248
16
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.245
17
HLX001 Helix Syndrome 46 0.244
18
48X005 48,xyyy 37 0.241
19
HYP060 Hyperinsulinism 55 0.241
20
DRM006 Dermatitis 63 0.239
21
P NRF023 Neurofibromatosis, Type Ii 77 0.229
22
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.228
23
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.223
24
P INF037 Inflammatory Bowel Disease 57 0.221
25
P HRT032 Heart Disease 78 0.218
26
CYS001 Cystic Fibrosis 84 0.217
27
P SZR006 Seizure Disorder 59 0.215
28
P DRR001 Diarrhea 55 0.212
29
HYP014 Hyperuricemia 52 0.212
30
P HYP750 Hypertriglyceridemia, Familial 62 0.211
31
P NRB010 Neuroblastoma 1 66 0.211
32
P VSC007 Vascular Disease 65 0.211
33
VSL002 Visual Epilepsy 58 0.209
34
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.208
35
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.208
36
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.208
37
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.208
38
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.208
39
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.208
40
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.208
41
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.208
42
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.208
43
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.208
44
P DDN001 Duodenal Ulcer 50 0.206
45
ISC004 Ischemia 62 0.204
46
P CRN018 Coronary Artery Anomaly 67 0.203
47
P GLM045 Glioma 64 0.202
48
CLT003 Colitis 63 0.201
49
P MLT020 Multiple Sclerosis 73 0.201
50
GLL048 Glial Tumor 48 0.200
51
P ADN016 Adenocarcinoma 65 0.199
52
P DBT009 Diabetes Mellitus 66 0.197
53
ALL026 Allergic Hypersensitivity Disease 65 0.197
54
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.197
55
OST012 Osteoarthritis 80 0.195
56
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.194
57
ART140 Arteries, Anomalies of 60 0.194
58
c GLL024 Gallbladder Disease 1 53 0.193
59
c PRC016 Pre-Eclampsia 63 0.192
60
P PRS040 Prostate Cancer 97 0.191
61
PRT037 Pertussis 66 0.189
62
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.184
63
INS024 Insulin-Like Growth Factor I 79 0.184
64
ATM095 Autoimmune Disease 62 0.184
65
CYT002 Cytokine Deficiency 46 0.183
66
P OST002 Osteoporosis 79 0.183
67
c HYP595 Hypertension, Essential 87 0.183
68
P HPT023 Hepatocellular Carcinoma 99 0.181
69
c CHR684 Chronic Kidney Disease 68 0.178
70
NNL006 Non-Alcoholic Steatohepatitis 53 0.178
71
P MYC007 Myocardial Infarction 74 0.177
72
HYP066 Hyperglycemia 63 0.176
73
P PSR002 Psoriasis 63 0.176
74
ULC004 Ulcerative Colitis 75 0.175
75
GLB002 Glioblastoma 74 0.173
76
GLB015 Glioblastoma Multiforme 60 0.173
77
P DRM053 Dermatitis, Atopic 68 0.173
78
c ACT210 Acute Respiratory Distress Syndrome 59 0.171
79
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.169
80
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.169
81
PST011 Pustulosis of Palm and Sole 51 0.167
82
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.166
83
P LKM002 Leukemia 69 0.164
84
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.164
85
PPT005 Peptic Ulcer Disease 60 0.164
86
P HNT016 Huntington Disease 72 0.163
87
P BPL003 Bipolar Disorder 59 0.161
88
P PNC035 Pancreatic Cancer 86 0.161
89
GLC003 Glucose Intolerance 55 0.161
90
c MJR024 Major Affective Disorder 9 42 0.161
91
c MJR022 Major Affective Disorder 8 39 0.161
92
CRH001 Crohn's Disease 75 0.159
93
c FTL070 Fetal Akinesia Deformation Sequence 2 33 0.159
94
P NRP001 Neuropathy 57 0.158
95
CHL014 Cholera 58 0.158
96
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.154
97
DFC004 Deficiency Anemia 77 0.153
98
P MYL006 Myeloid Leukemia 61 0.153
99
ADN018 Adenoma 60 0.153
100
PPL052 Papillomatosis, Confluent and Reticulated 34 0.152
101
47X002 47,xyy 49 0.150
102
HMN044 Human Immunodeficiency Virus Type 1 73 0.149
103
P ALZ034 Alzheimer Disease 90 0.148
104
P BLD134 Bladder Cancer 79 0.148
105
KRT009 Keratosis 52 0.146
106
HYP266 Hypoxia 58 0.146
107
c MGR028 Migraine with or Without Aura 1 70 0.145
108
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.145
109
P LNG032 Lung Cancer 99 0.145
110
P OVR042 Ovarian Cancer 89 0.144
111
ADR007 Adrenoleukodystrophy 72 0.143
112
LNG099 Lung Disease 62 0.142
113
NTR005 Nutritional Deficiency Disease 61 0.141
114
ADR022 Adrenomyeloneuropathy 39 0.140
115
c RHB024 Rhabdomyosarcoma 2 64 0.140
116
OST159 Osteogenic Sarcoma 67 0.139
117
CRB039 Cerebrovascular Disease 71 0.138
118
P RHM011 Rheumatoid Arthritis 82 0.138
119
BND020 Bone Disease 60 0.137
120
AGN016 Aging 58 0.136
121
c DWL002 Dowling-Degos Disease 1 59 0.136
122
c ACT071 Acute Kidney Failure 60 0.135
123
P GST053 Gastric Cancer 85 0.135
124
c PCH010 Pachyonychia Congenita 3 43 0.134
125
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.134
126
CNG034 Congestive Heart Failure 69 0.133
127
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 41 0.133
128
P ART022 Arthritis 71 0.132
129
P MSC003 Muscular Atrophy 52 0.132
130
ALC007 Alcohol Dependence 68 0.132
131
IRN002 Iron Metabolism Disease 58 0.132
132
P BRS044 Breast Adenocarcinoma 59 0.131
133
STR067 Stroke, Ischemic 82 0.131
134
PHN003 Phenylketonuria 73 0.130
135
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.128
136
HMC014 Homocysteinemia 54 0.128
137
RCK004 Rickets 70 0.128
138
P LYM031 Lymphocytic Leukemia 56 0.128
139
CLN015 Colon Adenocarcinoma 65 0.127
140
PPL022 Papilloma 56 0.125
141
P PRD008 Periodontitis 66 0.125
142
P TRN020 Turner Syndrome 66 0.125
143
BRN071 Brain Injury 51 0.125
144
P CRD132 Cardiac Conduction Defect 61 0.125
145
HMP009 Haemophilus Influenzae 46 0.125
146
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.123
147
P RTN024 Retinoblastoma 74 0.123
148
c FML008 Familial Retinoblastoma 46 0.123
149
SKN016 Skin Disease 64 0.123
150
P BCL017 B-Cell Lymphoma 61 0.122
151
ALL014 Allergic Encephalomyelitis 40 0.122
152
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.121
153
P MSC005 Muscular Dystrophy 68 0.121
154
DYS014 Dyspepsia 51 0.121
155
DWN001 Down Syndrome 70 0.121
156
c ACT075 Acute Myocardial Infarction 59 0.120
157
P ALP008 Alopecia 58 0.120
158
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.120
159
MDD011 Mood Disorder 62 0.120
160
P CHR345 Chronic Pain 52 0.120
161
c ACT027 Acute Pancreatitis 60 0.120
162
DBT010 Diabetic Neuropathy 56 0.119
163
SQM006 Squamous Cell Carcinoma 60 0.119
164
SPN186 Spinal Cord Injury 63 0.119
165
AST005 Asthma 80 0.118
167
c DNT047 Dentinogenesis Imperfecta Type 2 34 0.118
168
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.118
169
KRT002 Keratomalacia 47 0.117
170
HYP081 Hypolipoproteinemia 51 0.117
171
ATX019 Ataxia with Vitamin E Deficiency 46 0.117
172
THR024 Thrombosis 58 0.117
173
MTH071 Methane Production 26 0.117
174
ANG054 Angina Pectoris 66 0.117
175
P TRM003 Tremor 55 0.117
176
c MCR120 Microvascular Complications of Diabetes 7 48 0.116
177
c MCR113 Microvascular Complications of Diabetes 3 55 0.116
178
SQM002 Squamous Cell Papilloma 49 0.115
179
P LPS004 Lupus Erythematosus 62 0.115
180
c MCR130 Microvascular Complications of Diabetes 6 42 0.115
181
c MCR133 Microvascular Complications of Diabetes 4 42 0.115
182
CNS004 Constipation 59 0.115
183
SVR004 Severe Combined Immunodeficiency 74 0.115
184
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.114
185
P HPT021 Hepatitis 69 0.113
186
P PLY019 Polyneuropathy 55 0.113
187
P CTR002 Cataract 62 0.113
188
BCT022 Bacterial Infectious Disease 57 0.113
189
SRC014 Sarcoma 67 0.113
190
SPN035 Spindle Cell Sarcoma 57 0.113
191
P ECL001 Eclampsia 53 0.113
192
P GLM007 Glomerulonephritis 58 0.112
193
c SYS001 Systemic Lupus Erythematosus 88 0.110
194
CRB004 Cerebral Artery Occlusion 38 0.110
195
TXC005 Toxic Shock Syndrome 63 0.110
196
ANX004 Anoxia 44 0.109
197
P LNG064 Lung Cancer Susceptibility 3 79 0.109
198
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 55 0.108
199
ANX010 Anxiety 75 0.108
200
CNT047 Contact Dermatitis 58 0.108
201
MCS002 Mucositis 56 0.108
202
P PRP019 Peripheral Nervous System Disease 64 0.108
203
P CRD119 Cardiac Arrest 71 0.107
204
TTN003 Tetanus 62 0.107
205
P ART021 Arteriosclerosis 56 0.107
206
HLC007 Helicobacter Pylori Infection 61 0.106
207
PRT036 Peritonitis 66 0.106
208
c SML038 Small Cell Cancer of the Lung 67 0.105
209
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.105
210
c FML021 Familial Hypercholesterolemia 67 0.105
211
P TMP001 Temporal Lobe Epilepsy 53 0.105
212
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.104
213
P PLY014 Polycystic Kidney Disease 61 0.104
214
P PNC044 Pancreatitis 61 0.103
215
BRN024 Bronchitis 70 0.103
216
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.102
217
P LYM118 Lymphoma 70 0.101
218
c HNT004 Huntington Disease-Like 2 48 0.101
219
CHL004 Cholelithiasis 50 0.101
220
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.101
221
DNT012 Dental Caries 52 0.100
222
P PHC003 Pheochromocytoma 71 0.100
223
PRX001 Peroxisomal Disease 45 0.100
224
ADR040 Adrenal Gland Pheochromocytoma 51 0.099
225
NWC001 Newcastle Disease 45 0.099
226
ALL006 Allergic Asthma 56 0.099
227
P MCR115 Microvascular Complications of Diabetes 5 67 0.099
228
P ATR011 Atrial Fibrillation 67 0.098
229
c VRL010 Viral Hepatitis 56 0.098
230
GST040 Gastric Adenocarcinoma 67 0.098
231
P ACT008 Actinic Keratosis 50 0.098
232
GST033 Gestational Diabetes 58 0.097
233
P HYP098 Hypereosinophilic Syndrome 67 0.096
234
P RHN004 Rhinitis 59 0.095
235
CHL079 Children's Interstitial Lung Disease 27 0.095
236
P RTN016 Retinal Degeneration 56 0.094
237
PNC129 Pancreatic Adenocarcinoma 69 0.094
238
END057 Endometrial Cancer 74 0.093
239
c LKM063 Leukemia, Chronic Myeloid 74 0.093
240
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.092
241
HMS001 Hemosiderosis 54 0.092
242
MSL001 Measles 61 0.092
243
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.091
244
MSC007 Muscle Hypertrophy 65 0.091
245
IRR002 Irritable Bowel Syndrome 65 0.090
246
P RCT021 Rectum Cancer 54 0.090
247
IGR001 Ige Responsiveness, Atopic 61 0.090
248
GST045 Gastroenteritis 60 0.090
249
P RRH023 Rare Hereditary Hemochromatosis 41 0.090
250
c MCR129 Microvascular Complications of Diabetes 1 67 0.090
251
P PLM036 Pulmonary Fibrosis 66 0.089
252
IDP011 Idiopathic Interstitial Pneumonia 65 0.089
253
P HDC001 Headache 59 0.089
254
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.089
255
c ACT134 Acute Liver Failure 53 0.089
256
c HNT011 Huntington Disease-Like 3 37 0.089
257
PRP027 Peripheral Vascular Disease 72 0.089
258
P KDN017 Kidney Cancer 60 0.088
259
P INT068 Intestinal Disease 56 0.088
260
DBT004 Diabetic Polyneuropathy 48 0.088
261
LPT014 Leptin Deficiency or Dysfunction 72 0.088
262
P PLM037 Pulmonary Hypertension 69 0.088
263
c LKM071 Leukemia, Chronic Lymphocytic 81 0.088
264
ORL011 Oral Cancer 62 0.087
265
P ADL010 Adult Respiratory Distress Syndrome 61 0.087
266
AMN003 Amnestic Disorder 55 0.086
267
EYD002 Eye Disease 59 0.086
268
c FML035 Familial Hyperlipidemia 56 0.086
269
P HYP069 Hyperparathyroidism 64 0.086
270
MST005 Mastitis 55 0.086
271
c LKM004 Leukemia, B-Cell, Chronic 35 0.085
272
INS001 Insulinoma 60 0.085
273
ALL003 Allergic Rhinitis 69 0.084
274
KRT006 Keratoconjunctivitis 53 0.084
275
DRY001 Dry Eye Syndrome 50 0.084
276
P THL005 Thalassemia 62 0.084
278
STT004 Steatorrhea 39 0.083
279
KWS001 Kwashiorkor 46 0.082
280
c HPT003 Hepatitis a 60 0.082
281
P FML011 Familial Adenomatous Polyposis 73 0.082
282
TRN015 Transient Cerebral Ischemia 62 0.080
283
P SYS005 Systemic Scleroderma 68 0.080
284
ACR006 Aceruloplasminemia 74 0.079
285
KRT001 Keratoconjunctivitis Sicca 53 0.079
286
PSY004 Psychotic Disorder 68 0.078
287
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.078
288
P HMC002 Homocystinuria 52 0.078
289
TLN003 Telangiectasis 53 0.077
290
TXC020 Toxic Oil Syndrome 34 0.077
291
KRT019 Keratitis, Hereditary 69 0.076
292
MCR013 Microphthalmia 62 0.076
293
DBT002 Diabetic Autonomic Neuropathy 45 0.075
294
49X002 49,xxxxy Syndrome 39 0.075
295
BTN004 Biotin Deficiency 38 0.075
296
LYM133 Lymphoma, Hodgkin, Classic 70 0.075
297
VRC005 Varicose Veins 61 0.074
298
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.074
299
PST092 Posttransplant Acute Limbic Encephalitis 29 0.074
300
ART004 Aortic Atherosclerosis 47 0.074
301
MSC157 Muscular Dystrophy, Duchenne Type 70 0.073
302
CHP002 Chops Syndrome 41 0.073
303
MNN042 Meningioma, Radiation-Induced 64 0.073
304
P UVT001 Uveitis 58 0.072
305
c MNN043 Meningioma, Familial 74 0.072
306
SPN021 Spinal Meningioma 40 0.072
307
LYM002 Lymphoplasmacyte-Rich Meningioma 40 0.072
308
SCR001 Secretory Meningioma 38 0.072
309
NTR046 Neutrophil Migration 49 0.072
310
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.072
311
PLC008 Placenta Disease 51 0.071
312
SPL018 Splenomegaly 48 0.071
313
CRH005 Crohn's Colitis 56 0.071
314
P RHB003 Rhabdomyosarcoma 62 0.070
315
PRP080 Peripheral Artery Disease 51 0.070
316
P MJR007 Major Affective Disorder 1 44 0.070
317
OST017 Osteomyelitis 65 0.070
318
P CLC063 Celiac Disease 1 66 0.070
319
CLR109 Colorectal Adenocarcinoma 51 0.070
320
c MCL062 Mucolipidosis Ii Alpha/beta 67 0.069
321
DSS008 Disease of Mental Health 66 0.069
322
c ATM011 Autoimmune Hepatitis 63 0.069
323
P ALP009 Alopecia Areata 61 0.068
324
LYM027 Lymphopenia 58 0.068
325
c HYP272 Hypercholesterolemia, Familial, 3 44 0.068
326
HPT022 Hepatoblastoma 58 0.068
327
ILS001 Ileus 51 0.067
328
c FML001 Familial Atrial Fibrillation 67 0.067
329
DMY004 Demyelinating Disease 54 0.067
330
CRC021 Carcinosarcoma 62 0.066
331
P SJG008 Sjogren Syndrome 57 0.066
332
c BTT014 Beta-Thalassemia 73 0.066
333
P ICH004 Ichthyosis 55 0.066
334
c MJR003 Major Affective Disorder 6 34 0.066
335
c MJR006 Major Affective Disorder 5 34 0.066
336
ENC005 Encephalomalacia 37 0.066
337
HYP080 Hypogonadism 51 0.065
338
HYP064 Hypogonadotropism 40 0.065
339
c MJR008 Major Affective Disorder 2 35 0.065
340
c MJR023 Major Affective Disorder 7 34 0.065
341
c MJR004 Major Affective Disorder 4 29 0.065
342
P FTL001 Fetal Alcohol Syndrome 56 0.064
343
P SBS003 Substance Abuse 56 0.064
344
MST004 Mast Cell Neoplasm 40 0.064
345
EXT007 Extracutaneous Mastocytoma 39 0.064
346
c HYP768 Hyperlipoproteinemia, Type I 50 0.064
347
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.064
348
P LCH002 Lichen Planus 55 0.064
349
c FTL071 Fetal Akinesia Deformation Sequence 3 23 0.064
350
CRD223 Cardiac Arrhythmia 61 0.063
351
P MNC007 Monocytic Leukemia 52 0.063
353
c SCN007 Secondary Hyperparathyroidism 52 0.062
354
MYC006 Mycosis Fungoides 67 0.062
355
c HMC039 Hemochromatosis, Type 1 73 0.061
356
TRP004 Tropical Sprue 41 0.060
357
PRP016 Paraplegia 54 0.060
359
DFF005 Diffuse Large B-Cell Lymphoma 56 0.059
360
PYR016 Pyridoxine Deficiency 31 0.059
361
ATN005 Autonomic Dysfunction 48 0.059
362
c JVN010 Juvenile Rheumatoid Arthritis 67 0.058
363
TXC002 Toxic Encephalopathy 54 0.058
364
P TRC031 Trichorhinophalangeal Syndrome 41 0.058
365
P MRC003 Mercury Poisoning 47 0.058
366
AMN001 Amenorrhea 54 0.056
367
HYP457 Hypertrophic Scars 44 0.056
368
OVR063 Overnutrition 47 0.055
369
CRP001 Carpal Tunnel Syndrome 68 0.054
370
DBT008 Diabetic Angiopathy 42 0.054
371
ACD008 Acid-Labile Subunit Deficiency 55 0.054
372
BRS099 Breast Ductal Carcinoma 63 0.054
373
PLL012 Pollen Allergy 46 0.054
374
CHD004 Chudley-Mccullough Syndrome 44 0.054
375
ABD010 Abdominal Wall Defect 37 0.052
376
FSC004 Fasciitis 47 0.051
377
c ATM006 Autoimmune Lymphoproliferative Syndrome 73 0.051
378
INT052 Intestinal Volvulus 44 0.051
379
GST037 Gastroparesis 52 0.050
380
ORL013 Oral Lichen Planus 47 0.050
381
MCN017 Meconium Ileus 54 0.049
382
P OVR046 Ovarian Cyst 50 0.049
383
P LMY004 Leiomyosarcoma 63 0.048
384
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 63 0.047
385
P FRD012 Friedreich Ataxia 1 65 0.047
386
c DRM054 Dermatitis, Atopic, 2 45 0.047
387
NRD001 Neurodermatitis 40 0.047
388
P MGR001 Migraine Without Aura 47 0.046
389
BRR012 Berardinelli-Seip Congenital Lipodystrophy 46 0.046
390
BRT005 Barth Syndrome 52 0.046
391
BWN001 Bowen-Conradi Syndrome 49 0.046
392
FLL008 Folliculitis 46 0.046
393
RFR003 Refractive Error 44 0.046
394
GST009 Gastroschisis 52 0.045
395
P CRB059 Cerebellar Degeneration 38 0.045
396
HDR003 Hidradenitis 48 0.044
397
NCR007 Necrotizing Fasciitis 47 0.044
398
c ATM099 Autoimmune Uveitis 45 0.044
399
c RNG008 Ring Chromosome 13 29 0.044
400
P FTL069 Fetal Akinesia Deformation Sequence 1 55 0.044
401
CMP002 Campylobacteriosis 48 0.044
402
HDR002 Hidradenitis Suppurativa 58 0.043
403
ADR016 Adrenal Cortical Carcinoma 51 0.043
404
HYP006 Hypertensive Heart Disease 49 0.043
405
SCH038 Schopf-Schulz-Passarge Syndrome 48 0.042
406
P LPS002 Liposarcoma 62 0.041
407
INF118 Inflammatory Myopathy with Abundant Macrophages 29 0.041
408
P BRS053 Breast Fibroadenoma 49 0.041
409
PLP001 Pulpitis 48 0.041
410
c EST002 Estrogen-Receptor Negative Breast Cancer 43 0.041
411
HYP189 Hypoadrenalism 39 0.040
412
MSC152 Muscular Dystrophy, Becker Type 60 0.039
413
ONC002 Onchocerciasis 50 0.039
414
LRY027 Laryngeal Papillomatosis 24 0.039
415
END021 Endomyocardial Fibrosis 50 0.038
416
PLM029 Palmoplantar Keratosis 48 0.038
417
c HNT010 Huntington Disease-Like 1 49 0.037
418
IMM001 Immune-Complex Glomerulonephritis 40 0.037
419
c MYT029 Myotonia Congenita, Autosomal Recessive 41 0.036
420
P BNG002 Benign Meningioma 38 0.036
421
HYP855 Hyperpigmentation of the Skin 29 0.036
422
c HMG003 Hemoglobin E Disease 43 0.034
423
HYP784 Hypogonadism, Male 39 0.034
424
SCT002 Scotoma 38 0.034
425
DDN027 Duodenum Disease 36 0.034
426
NRX001 Neuroaxonal Dystrophy 33 0.034
427
c THR082 Thrombophilia Due to Activated Protein C Resistance 61 0.033
428
P STR035 Streptococcal Group a Invasive Disease 24 0.033
429
BLP046 Blepharophimosis, Ptosis, and Epicanthus Inversus 52 0.031
Content
Loading form....