Search results for linoleic acid

424 hits were found for linoleic acid

# Family MCID Name MIFTS Score
1
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.450
2
FTT001 Fatty Liver Disease 61 0.363
3
P CLR023 Colorectal Cancer 99 0.321
4
P LVR013 Liver Disease 68 0.313
5
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.306
6
ATH013 Atherosclerosis Susceptibility 65 0.280
7
P KDN018 Kidney Disease 72 0.272
8
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.264
9
LPD008 Lipid Metabolism Disorder 62 0.263
10
P CRN300 Coronary Heart Disease 1 63 0.262
11
c HYP836 Hypercholesterolemia, Familial, 1 73 0.254
12
P BRS047 Breast Cancer 97 0.252
13
BNR002 Bone Resorption Disease 48 0.247
14
LVR012 Liver Cirrhosis 62 0.240
15
HLX001 Helix Syndrome 47 0.236
16
HYP060 Hyperinsulinism 54 0.236
17
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.234
18
48X005 48,xyyy 39 0.230
19
DRM006 Dermatitis 61 0.226
20
c NRF023 Neurofibromatosis, Type Ii 80 0.223
21
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.218
22
HYP014 Hyperuricemia 52 0.212
23
CYS001 Cystic Fibrosis 81 0.211
24
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.210
25
P HYP750 Hypertriglyceridemia, Familial 62 0.208
26
P SZR006 Seizure Disorder 56 0.208
27
P VSC007 Vascular Disease 63 0.206
28
P DRR001 Diarrhea 55 0.206
29
P NRB001 Neuroblastoma 72 0.205
30
P HRT032 Heart Disease 75 0.203
31
P INF037 Inflammatory Bowel Disease 54 0.203
32
VSL002 Visual Epilepsy 59 0.202
33
P DDN001 Duodenal Ulcer 52 0.200
34
LPP008 Lipoprotein Quantitative Trait Locus 62 0.199
35
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.195
36
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.195
37
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.195
38
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.195
39
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.195
40
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.195
41
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.195
42
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.195
43
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.195
44
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.195
45
c PRC016 Pre-Eclampsia 63 0.194
46
OST012 Osteoarthritis 78 0.194
47
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.193
48
CLT003 Colitis 62 0.190
49
ISC004 Ischemia 58 0.189
50
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.188
51
c GLL024 Gallbladder Disease 1 53 0.188
52
ART140 Arteries, Anomalies of 52 0.188
53
P GLM045 Glioma 63 0.187
54
P PRS040 Prostate Cancer 97 0.186
55
GLL048 Glial Tumor 45 0.185
56
CYT002 Cytokine Deficiency 42 0.184
57
PRT037 Pertussis 65 0.184
58
P DBT009 Diabetes Mellitus 64 0.184
59
P ADN016 Adenocarcinoma 64 0.184
60
ATM095 Autoimmune Disease 62 0.182
61
P HPT023 Hepatocellular Carcinoma 100 0.180
62
INS024 Insulin-Like Growth Factor I 79 0.180
63
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.179
64
NNL006 Non-Alcoholic Steatohepatitis 54 0.179
65
P DRM053 Dermatitis, Atopic 66 0.178
66
c CHR684 Chronic Kidney Disease 70 0.172
67
ALL026 Allergic Hypersensitivity Disease 62 0.171
68
HYP066 Hyperglycemia 61 0.170
69
P PSR002 Psoriasis 62 0.170
70
GLB015 Glioblastoma Multiforme 75 0.169
71
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.169
72
P MYC007 Myocardial Infarction 70 0.166
73
c HYP595 Hypertension, Essential 84 0.166
74
P CRD246 Cardiovascular System Disease 57 0.164
75
P OST002 Osteoporosis 74 0.163
76
P MLT020 Multiple Sclerosis 72 0.161
77
PST011 Pustulosis of Palm and Sole 52 0.160
78
P LKM002 Leukemia 68 0.160
79
P HNT016 Huntington Disease 72 0.160
80
ULC004 Ulcerative Colitis 73 0.160
81
P BPL003 Bipolar Disorder 56 0.159
82
c MJR024 Major Affective Disorder 9 41 0.159
83
c MJR022 Major Affective Disorder 8 38 0.159
84
GLC003 Glucose Intolerance 54 0.159
85
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.158
86
PPT005 Peptic Ulcer Disease 59 0.158
87
P PNC035 Pancreatic Cancer 84 0.155
88
PPL052 Papillomatosis, Confluent and Reticulated 33 0.155
89
P NRP001 Neuropathy 56 0.155
90
P MYL006 Myeloid Leukemia 60 0.154
91
CHL014 Cholera 59 0.154
92
CRH001 Crohn's Disease 74 0.152
93
P ALZ034 Alzheimer Disease 88 0.151
94
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.148
95
DFC004 Deficiency Anemia 70 0.148
96
ADN018 Adenoma 59 0.147
97
P LNG032 Lung Cancer 98 0.146
98
HMN044 Human Immunodeficiency Virus Type 1 71 0.145
99
KRT009 Keratosis 51 0.145
100
LNG099 Lung Disease 60 0.144
101
P BLD134 Bladder Cancer 79 0.141
102
HYP266 Hypoxia 57 0.139
103
NTR005 Nutritional Deficiency Disease 62 0.139
104
c RHB024 Rhabdomyosarcoma 2 67 0.139
105
P OVR042 Ovarian Cancer 88 0.139
106
ADR007 Adrenoleukodystrophy 75 0.139
107
c MGR028 Migraine with or Without Aura 1 67 0.139
108
P GST053 Gastric Cancer 83 0.138
109
OST159 Osteogenic Sarcoma 66 0.138
110
ADR022 Adrenomyeloneuropathy 38 0.137
111
c DWL002 Dowling-Degos Disease 1 58 0.136
112
47X002 47,xyy 49 0.135
113
P BND020 Bone Disease 59 0.135
114
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.134
115
RCK004 Rickets 68 0.133
116
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.132
117
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.132
118
SKN016 Skin Disease 63 0.132
119
c PCH010 Pachyonychia Congenita 3 44 0.132
120
CNG034 Congestive Heart Failure 69 0.131
121
c ACT071 Acute Kidney Failure 60 0.131
122
P BRS044 Breast Adenocarcinoma 59 0.131
123
P ART022 Arthritis 69 0.131
124
P MSC003 Muscular Atrophy 52 0.130
125
IRN002 Iron Metabolism Disease 57 0.128
126
ALC007 Alcohol Dependence 66 0.128
127
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.128
128
PHN003 Phenylketonuria 75 0.127
129
P PRD008 Periodontitis 64 0.127
130
STR067 Stroke, Ischemic 81 0.127
131
P ATS364 Autism 70 0.125
132
HMC014 Homocysteinemia 53 0.125
133
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.125
134
DWN001 Down Syndrome 70 0.124
135
PPL022 Papilloma 54 0.123
136
CRD132 Cardiac Conduction Defect 58 0.123
137
CLN015 Colon Adenocarcinoma 65 0.122
138
P BCL017 B-Cell Lymphoma 58 0.121
139
P TRN020 Turner Syndrome 67 0.121
140
HMP009 Haemophilus Influenzae 43 0.121
141
ATX019 Ataxia with Vitamin E Deficiency 42 0.121
142
ALL014 Allergic Encephalomyelitis 38 0.120
143
P RHM011 Rheumatoid Arthritis 80 0.120
144
P RTN024 Retinoblastoma 73 0.120
145
c FML008 Familial Retinoblastoma 53 0.120
146
c ACT027 Acute Pancreatitis 60 0.120
147
P ALP008 Alopecia 54 0.119
149
P MSC005 Muscular Dystrophy 66 0.118
150
MDD011 Mood Disorder 62 0.118
151
DBT010 Diabetic Neuropathy 54 0.118
152
CRB039 Cerebrovascular Disease 67 0.118
153
MTH071 Methane Production 26 0.118
154
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.118
155
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.118
156
BRN071 Brain Injury 49 0.118
157
c ACT075 Acute Myocardial Infarction 57 0.118
158
HYP081 Hypolipoproteinemia 51 0.117
159
c ATS007 Autism Spectrum Disorder 67 0.116
160
BCT022 Bacterial Infectious Disease 56 0.116
161
KRT002 Keratomalacia 47 0.116
162
c MCR120 Microvascular Complications of Diabetes 7 47 0.115
163
AST005 Asthma 76 0.115
164
c DBT099 Diabetes Mellitus, Type I 65 0.115
165
c MCR113 Microvascular Complications of Diabetes 3 52 0.115
166
SRC014 Sarcoma 65 0.115
167
SPN035 Spindle Cell Sarcoma 53 0.115
168
SPN186 Spinal Cord Injury 60 0.115
169
c MCR130 Microvascular Complications of Diabetes 6 41 0.114
170
c MCR133 Microvascular Complications of Diabetes 4 41 0.114
171
P TRM003 Tremor 54 0.114
172
AGN016 Aging 56 0.114
173
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.114
174
ANG054 Angina Pectoris 66 0.114
175
SQM002 Squamous Cell Papilloma 46 0.114
176
SQM006 Squamous Cell Carcinoma 60 0.113
177
CNS004 Constipation 58 0.112
178
SVR004 Severe Combined Immunodeficiency 73 0.112
179
THR024 Thrombosis 57 0.112
180
P ECL001 Eclampsia 50 0.112
181
P PLY019 Polyneuropathy 56 0.111
182
P HPT021 Hepatitis 67 0.111
183
CRB004 Cerebral Artery Occlusion 45 0.110
184
TXC005 Toxic Shock Syndrome 62 0.109
185
P GLM007 Glomerulonephritis 57 0.109
186
P CTR002 Cataract 60 0.109
187
P CHR345 Chronic Pain 44 0.109
188
P LNG064 Lung Cancer Susceptibility 3 78 0.108
189
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.108
190
c SYS001 Systemic Lupus Erythematosus 86 0.108
191
CNT047 Contact Dermatitis 58 0.107
192
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.106
193
P PRP019 Peripheral Nervous System Disease 58 0.106
194
ANX004 Anoxia 40 0.106
195
MCS002 Mucositis 56 0.105
196
TTN003 Tetanus 65 0.105
197
P ART021 Arteriosclerosis 54 0.104
198
ANX010 Anxiety 73 0.104
199
P RHN004 Rhinitis 57 0.104
200
HLC007 Helicobacter Pylori Infection 59 0.104
201
PRT036 Peritonitis 64 0.104
202
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.103
203
P TMP001 Temporal Lobe Epilepsy 50 0.103
204
c FML021 Familial Hypercholesterolemia 66 0.103
205
P PLY014 Polycystic Kidney Disease 62 0.103
206
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.102
207
P LPS004 Lupus Erythematosus 61 0.101
208
BRN024 Bronchitis 68 0.101
209
ALL006 Allergic Asthma 56 0.101
210
c SML038 Small Cell Cancer of the Lung 65 0.100
211
DNT012 Dental Caries 53 0.100
212
GST033 Gestational Diabetes 61 0.099
213
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.099
214
P PNC044 Pancreatitis 61 0.099
215
c HNT004 Huntington Disease-Like 2 50 0.099
216
P PHC003 Pheochromocytoma 71 0.098
217
ADR040 Adrenal Gland Pheochromocytoma 46 0.098
218
NWC001 Newcastle Disease 45 0.098
219
P MCR115 Microvascular Complications of Diabetes 5 66 0.097
220
CHL004 Cholelithiasis 49 0.097
221
GST040 Gastric Adenocarcinoma 70 0.097
222
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.097
223
PRX001 Peroxisomal Disease 46 0.096
224
P ACT008 Actinic Keratosis 53 0.096
225
c VRL010 Viral Hepatitis 52 0.095
226
P ATR011 Atrial Fibrillation 66 0.095
227
P HYP098 Hypereosinophilic Syndrome 67 0.094
228
P RTN016 Retinal Degeneration 53 0.093
229
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.093
230
CHL079 Children's Interstitial Lung Disease 26 0.093
231
ALL003 Allergic Rhinitis 67 0.092
232
P ADL010 Adult Respiratory Distress Syndrome 65 0.092
233
END057 Endometrial Cancer 74 0.092
234
PNC129 Pancreatic Adenocarcinoma 68 0.091
235
P PLM036 Pulmonary Fibrosis 65 0.091
236
HMS001 Hemosiderosis 54 0.091
237
MSL001 Measles 62 0.090
238
IRR002 Irritable Bowel Syndrome 65 0.090
239
MSC007 Muscle Hypertrophy 64 0.089
240
c MCR129 Microvascular Complications of Diabetes 1 66 0.089
241
GST045 Gastroenteritis 59 0.089
242
P RRH023 Rare Hereditary Hemochromatosis 41 0.089
243
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.089
244
P INT068 Intestinal Disease 53 0.088
245
IGR001 Ige Responsiveness, Atopic 59 0.088
246
P RCT021 Rectum Cancer 52 0.088
247
c ACT134 Acute Liver Failure 56 0.088
248
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.087
249
P KDN017 Kidney Cancer 60 0.087
250
DBT004 Diabetic Polyneuropathy 49 0.087
251
c HNT011 Huntington Disease-Like 3 38 0.087
252
EYD002 Eye Disease 58 0.087
253
PRP027 Peripheral Vascular Disease 71 0.087
254
LPT014 Leptin Deficiency or Dysfunction 74 0.086
255
ORL011 Oral Cancer 60 0.086
256
LSH001 Leishmaniasis 63 0.085
257
P HDC001 Headache 57 0.085
258
MST005 Mastitis 53 0.085
259
P KLZ004 Kala-Azar 1 41 0.085
260
P LKM071 Leukemia, Chronic Lymphocytic 79 0.085
261
DRY001 Dry Eye Syndrome 47 0.084
262
AMN003 Amnestic Disorder 54 0.084
263
P GLM040 Glioma Susceptibility 1 81 0.084
264
P HYP069 Hyperparathyroidism 63 0.084
265
P THL005 Thalassemia 60 0.084
266
c FML035 Familial Hyperlipidemia 55 0.084
267
P PLM037 Pulmonary Hypertension 67 0.083
268
INS001 Insulinoma 60 0.083
269
KRT006 Keratoconjunctivitis 53 0.083
271
P FML011 Familial Adenomatous Polyposis 72 0.081
272
c HPT003 Hepatitis a 62 0.080
273
KWS001 Kwashiorkor 44 0.080
274
P SYS005 Systemic Scleroderma 68 0.078
275
KRT001 Keratoconjunctivitis Sicca 49 0.078
276
TRN015 Transient Cerebral Ischemia 63 0.077
277
PSY004 Psychotic Disorder 67 0.077
278
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.076
279
P HMC002 Homocystinuria 53 0.076
280
TXC020 Toxic Oil Syndrome 33 0.076
281
TLN003 Telangiectasis 52 0.076
282
KRT019 Keratitis, Hereditary 65 0.075
283
DBT002 Diabetic Autonomic Neuropathy 41 0.075
284
MCR013 Microphthalmia 57 0.075
285
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.074
286
PST092 Posttransplant Acute Limbic Encephalitis 29 0.073
287
49X006 49, Xxxxy Syndrome 41 0.073
288
MNN042 Meningioma, Radiation-Induced 62 0.073
289
BTN004 Biotin Deficiency 38 0.073
290
c MNN043 Meningioma, Familial 74 0.073
291
VRC005 Varicose Veins 60 0.073
292
ART004 Aortic Atherosclerosis 47 0.072
293
SPN021 Spinal Meningioma 50 0.072
294
SCR001 Secretory Meningioma 41 0.072
295
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.072
296
CHP002 Chops Syndrome 44 0.071
297
MSC157 Muscular Dystrophy, Duchenne Type 72 0.071
298
P UVT001 Uveitis 57 0.071
299
LYM133 Lymphoma, Hodgkin, Classic 69 0.071
300
NTR046 Neutrophil Migration 50 0.071
301
SPL018 Splenomegaly 48 0.070
302
P CLC063 Celiac Disease 1 66 0.070
303
P RHB003 Rhabdomyosarcoma 63 0.069
304
PRP080 Peripheral Artery Disease 53 0.069
305
CLR109 Colorectal Adenocarcinoma 51 0.069
306
BRC012 Brucellosis 64 0.069
307
CRH005 Crohn's Colitis 53 0.069
308
P MJR007 Major Affective Disorder 1 43 0.068
309
OST017 Osteomyelitis 64 0.068
310
c ATM011 Autoimmune Hepatitis 63 0.068
311
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.068
312
P ALP009 Alopecia Areata 60 0.068
313
LYM027 Lymphopenia 58 0.068
314
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.067
315
DSS008 Disease of Mental Health 58 0.067
316
RDN001 Reading Disorder 40 0.067
317
HPT022 Hepatoblastoma 56 0.066
318
c BTT014 Beta-Thalassemia 74 0.066
319
P ICH004 Ichthyosis 54 0.066
320
DMY004 Demyelinating Disease 52 0.066
321
ILS001 Ileus 51 0.066
322
c HYP272 Hypercholesterolemia, Familial, 3 44 0.065
323
P SJG008 Sjogren Syndrome 61 0.065
324
c MJR003 Major Affective Disorder 6 33 0.065
325
c MJR006 Major Affective Disorder 5 33 0.065
326
P MNC007 Monocytic Leukemia 53 0.065
327
c FML001 Familial Atrial Fibrillation 65 0.064
328
CRC021 Carcinosarcoma 62 0.064
329
c HYP768 Hyperlipoproteinemia, Type I 67 0.064
330
ENC005 Encephalomalacia 43 0.064
331
HYP080 Hypogonadism 50 0.064
332
c MJR008 Major Affective Disorder 2 35 0.064
333
c MJR023 Major Affective Disorder 7 33 0.064
334
c MJR004 Major Affective Disorder 4 28 0.064
335
c FTL071 Fetal Akinesia Deformation Sequence 3 28 0.064
336
P FTL001 Fetal Alcohol Syndrome 57 0.064
338
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.063
339
VSC003 Visceral Leishmaniasis 55 0.063
340
P LCH002 Lichen Planus 53 0.063
341
MST004 Mast Cell Neoplasm 42 0.063
342
EXT007 Extracutaneous Mastocytoma 38 0.063
343
CRD223 Cardiac Arrhythmia 60 0.062
344
P SBS003 Substance Abuse 55 0.062
345
c SCN007 Secondary Hyperparathyroidism 51 0.061
346
PRP016 Paraplegia 52 0.060
347
MYC006 Mycosis Fungoides 66 0.059
348
c HMC039 Hemochromatosis, Type 1 74 0.059
349
TRP004 Tropical Sprue 41 0.059
351
DFF005 Diffuse Large B-Cell Lymphoma 55 0.058
352
PYR016 Pyridoxine Deficiency 30 0.058
353
P TRC031 Trichorhinophalangeal Syndrome 40 0.057
354
ATN005 Autonomic Dysfunction 46 0.057
355
P MRC003 Mercury Poisoning 48 0.057
356
c JVN010 Juvenile Rheumatoid Arthritis 64 0.056
357
HYP457 Hypertrophic Scars 42 0.056
358
TXC002 Toxic Encephalopathy 53 0.055
359
AMN001 Amenorrhea 54 0.054
360
OVR063 Overnutrition 44 0.054
361
ACD008 Acid-Labile Subunit Deficiency 54 0.054
362
CHD004 Chudley-Mccullough Syndrome 46 0.054
363
DBT008 Diabetic Angiopathy 44 0.053
364
CRP001 Carpal Tunnel Syndrome 67 0.053
365
BRS099 Breast Ductal Carcinoma 62 0.052
366
PLL012 Pollen Allergy 46 0.052
367
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.051
368
ABD010 Abdominal Wall Defect 36 0.051
369
FSC004 Fasciitis 50 0.050
370
VLV047 Volvulus of Midgut 49 0.049
371
GST037 Gastroparesis 54 0.049
372
c JVN061 Juvenile Arthritis 60 0.048
373
ORL013 Oral Lichen Planus 45 0.048
374
FLL008 Folliculitis 46 0.047
375
P LMY004 Leiomyosarcoma 63 0.047
376
MCN017 Meconium Ileus 52 0.047
377
P OVR046 Ovarian Cyst 47 0.047
378
BWN001 Bowen-Conradi Syndrome 52 0.046
379
P MGR001 Migraine Without Aura 49 0.046
380
P FRD001 Friedreich Ataxia 64 0.045
381
BRT005 Barth Syndrome 57 0.045
382
c ATM099 Autoimmune Uveitis 45 0.045
383
BRR012 Berardinelli-Seip Congenital Lipodystrophy 49 0.045
384
c DRM054 Dermatitis, Atopic, 2 44 0.045
385
NRD001 Neurodermatitis 35 0.045
386
GST009 Gastroschisis 53 0.044
387
PLP001 Pulpitis 49 0.044
388
P CRB059 Cerebellar Degeneration 37 0.044
389
ADR016 Adrenal Cortical Carcinoma 48 0.043
390
NCR007 Necrotizing Fasciitis 48 0.043
391
c RNG008 Ring Chromosome 13 31 0.043
392
ACR006 Aceruloplasminemia 65 0.043
393
P FTL069 Fetal Akinesia Deformation Sequence 1 64 0.043
394
HDR003 Hidradenitis 49 0.043
395
CMP002 Campylobacteriosis 46 0.043
396
BLP046 Blepharophimosis, Ptosis, and Epicanthus Inversus 54 0.042
397
OLG003 Oligohydramnios 51 0.042
398
HYP006 Hypertensive Heart Disease 49 0.042
399
RFR003 Refractive Error 43 0.042
400
HDR002 Hidradenitis Suppurativa 55 0.041
401
SCH038 Schopf-Schulz-Passarge Syndrome 55 0.041
402
P ATX024 Ataxia-Oculomotor Apraxia 3 44 0.041
403
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.041
404
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.040
405
P LPS002 Liposarcoma 65 0.040
406
P BRS053 Breast Fibroadenoma 49 0.040
407
c EST002 Estrogen-Receptor Negative Breast Cancer 45 0.040
408
MSC152 Muscular Dystrophy, Becker Type 63 0.038
409
LRY027 Laryngeal Papillomatosis 23 0.038
410
ONC002 Onchocerciasis 52 0.037
411
END021 Endomyocardial Fibrosis 49 0.037
412
PLM029 Palmoplantar Keratosis 47 0.037
413
c HNT010 Huntington Disease-Like 1 53 0.036
414
c HMG003 Hemoglobin E Disease 45 0.036
415
IMM001 Immune-Complex Glomerulonephritis 40 0.036
416
SCT002 Scotoma 44 0.035
417
c MYT029 Myotonia Congenita, Autosomal Recessive 41 0.035
418
HYP784 Hypogonadism, Male 40 0.035
419
P BNG002 Benign Meningioma 39 0.035
420
DDN027 Duodenum Disease 37 0.035
421
HYP855 Hyperpigmentation of the Skin 27 0.035
422
c THR082 Thrombophilia Due to Activated Protein C Resistance 61 0.034
423
NRX001 Neuroaxonal Dystrophy 35 0.034
424
P STR035 Streptococcal Group a Invasive Disease 23 0.033
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