Search results for Resveratrol

793 hits were found for Resveratrol

# Family MCID Name MIFTS Score
1
P CLR023 Colorectal Cancer 100 0.255
2
FTT001 Fatty Liver Disease 63 0.219
3
HYP066 Hyperglycemia 63 0.216
4
P LVR013 Liver Disease 71 0.194
5
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.194
6
ISC004 Ischemia 62 0.188
7
P ALZ034 Alzheimer Disease 90 0.183
8
P OVR042 Ovarian Cancer 89 0.176
9
AGN016 Aging 58 0.171
10
P GLM045 Glioma 64 0.165
11
GLL048 Glial Tumor 48 0.165
12
P PRS040 Prostate Cancer 97 0.162
13
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.162
14
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.160
15
GLB002 Glioblastoma 74 0.158
16
GLB015 Glioblastoma Multiforme 60 0.158
17
c MCR113 Microvascular Complications of Diabetes 3 55 0.156
18
c MCR120 Microvascular Complications of Diabetes 7 48 0.156
19
c MCR130 Microvascular Complications of Diabetes 6 42 0.156
20
c MCR133 Microvascular Complications of Diabetes 4 42 0.156
21
P HPT023 Hepatocellular Carcinoma 99 0.154
22
P BCL017 B-Cell Lymphoma 61 0.154
23
P BRS047 Breast Cancer 99 0.148
24
P PNC035 Pancreatic Cancer 86 0.144
25
LPD008 Lipid Metabolism Disorder 64 0.144
26
ATH013 Atherosclerosis Susceptibility 68 0.142
27
P NRB010 Neuroblastoma 1 66 0.142
28
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.139
29
CRB004 Cerebral Artery Occlusion 38 0.139
31
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.137
32
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.137
33
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.137
34
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.137
35
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.137
36
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.137
37
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.137
38
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.137
39
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.137
40
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.137
41
P DBT009 Diabetes Mellitus 66 0.135
42
BRN071 Brain Injury 51 0.135
43
c ACT027 Acute Pancreatitis 60 0.133
44
c PCH010 Pachyonychia Congenita 3 43 0.133
45
HYP266 Hypoxia 58 0.130
46
CYT002 Cytokine Deficiency 46 0.130
47
P SKN015 Skin Carcinoma 67 0.128
48
P PRD008 Periodontitis 66 0.128
49
P VSC007 Vascular Disease 65 0.128
50
P CRN300 Coronary Heart Disease 1 59 0.128
51
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.126
52
P PNC044 Pancreatitis 61 0.126
53
P LYM031 Lymphocytic Leukemia 56 0.126
54
P LNG032 Lung Cancer 99 0.123
55
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.123
56
SPN186 Spinal Cord Injury 63 0.121
57
P MCR115 Microvascular Complications of Diabetes 5 67 0.118
58
P LNG064 Lung Cancer Susceptibility 3 79 0.116
59
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.116
60
P OST002 Osteoporosis 79 0.113
61
c ATR087 Atrial Standstill 1 76 0.113
62
c HYP836 Hypercholesterolemia, Familial, 1 74 0.113
63
P PLY011 Polycystic Ovary Syndrome 58 0.113
64
HYP060 Hyperinsulinism 55 0.113
65
48X005 48,xyyy 37 0.113
66
P GST053 Gastric Cancer 85 0.110
67
P ADN016 Adenocarcinoma 65 0.110
68
c ACT210 Acute Respiratory Distress Syndrome 59 0.110
69
OST012 Osteoarthritis 80 0.107
70
P HRT032 Heart Disease 78 0.107
71
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.107
72
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.107
73
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.107
74
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.107
75
P HNT016 Huntington Disease 72 0.105
76
P END044 Endometriosis 63 0.105
77
MYL069 Myeloma, Multiple 85 0.102
78
STR067 Stroke, Ischemic 82 0.102
79
P LKM002 Leukemia 69 0.102
80
P LKM062 Leukemia, Acute Lymphoblastic 68 0.102
81
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.102
82
CLT003 Colitis 63 0.102
83
ART140 Arteries, Anomalies of 60 0.102
84
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.102
85
CRB039 Cerebrovascular Disease 71 0.099
86
MLN008 Melanoma 68 0.099
87
P INF037 Inflammatory Bowel Disease 57 0.099
88
P KDN018 Kidney Disease 73 0.095
89
SQM006 Squamous Cell Carcinoma 60 0.095
90
TRM010 Traumatic Brain Injury 54 0.095
91
NNL006 Non-Alcoholic Steatohepatitis 53 0.095
92
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.092
93
P CRN018 Coronary Artery Anomaly 67 0.092
94
c RHB024 Rhabdomyosarcoma 2 64 0.092
95
ATM095 Autoimmune Disease 62 0.092
96
GLC003 Glucose Intolerance 55 0.092
97
BNR002 Bone Resorption Disease 51 0.092
98
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.089
99
c HYP595 Hypertension, Essential 87 0.089
100
P BLD134 Bladder Cancer 79 0.089
101
P MDL005 Medulloblastoma 78 0.089
102
ULC004 Ulcerative Colitis 75 0.089
103
c CHR684 Chronic Kidney Disease 68 0.089
104
OST159 Osteogenic Sarcoma 67 0.089
105
LNG099 Lung Disease 62 0.089
106
ADN018 Adenoma 60 0.089
107
EYD002 Eye Disease 59 0.089
108
BRN004 Brain Edema 57 0.089
109
P LTR001 Lateral Sclerosis 56 0.089
110
CRV035 Cervical Cancer 77 0.085
111
CNG034 Congestive Heart Failure 69 0.085
112
P MSC005 Muscular Dystrophy 68 0.085
113
THY029 Thyroid Carcinoma 62 0.085
114
c LKM061 Leukemia, Acute Myeloid 84 0.082
115
SVR004 Severe Combined Immunodeficiency 74 0.082
116
P DMN002 Dementia 68 0.082
117
P INF032 Infertility 60 0.082
118
TLN003 Telangiectasis 53 0.082
119
IMP005 Impotence 53 0.082
120
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.082
121
P PRK057 Parkinson Disease, Late-Onset 77 0.078
122
P RTN024 Retinoblastoma 74 0.078
123
c LKM063 Leukemia, Chronic Myeloid 74 0.078
124
CLN015 Colon Adenocarcinoma 65 0.078
125
c PRC016 Pre-Eclampsia 63 0.078
126
ACT119 Acute Promyelocytic Leukemia 63 0.078
127
ORL011 Oral Cancer 62 0.078
128
CHL068 Cholestasis 61 0.078
129
P MYL006 Myeloid Leukemia 61 0.078
130
c DWL002 Dowling-Degos Disease 1 59 0.078
131
RNL077 Renal Fibrosis 49 0.078
132
c FML008 Familial Retinoblastoma 46 0.078
133
CRT015 Carotid Artery Occlusion 44 0.078
134
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.078
135
P ATX030 Ataxia-Telangiectasia 83 0.074
136
INS024 Insulin-Like Growth Factor I 79 0.074
137
P NRF023 Neurofibromatosis, Type Ii 77 0.074
138
P MYC007 Myocardial Infarction 74 0.074
139
MSC157 Muscular Dystrophy, Duchenne Type 70 0.074
140
ALL003 Allergic Rhinitis 69 0.074
141
P ATS364 Autism 68 0.074
142
P NSP012 Nasopharyngeal Carcinoma 67 0.074
143
RTN017 Retinal Detachment 62 0.074
144
P RHN004 Rhinitis 59 0.074
145
P NRP001 Neuropathy 57 0.074
146
VSC002 Vascular Dementia 57 0.074
147
P MSC003 Muscular Atrophy 52 0.074
148
DGN001 Degenerative Disc Disease 49 0.074
149
P BNG032 Benign Mesothelioma 47 0.074
150
ANX004 Anoxia 44 0.074
151
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.070
152
c SML038 Small Cell Cancer of the Lung 67 0.070
153
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.070
154
P TRN020 Turner Syndrome 66 0.070
155
DPR016 Depression 64 0.070
156
P ENC018 Encephalopathy 64 0.070
157
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.070
158
GT001 Gout 63 0.070
159
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.070
160
GST033 Gestational Diabetes 58 0.070
161
P MLN007 Male Infertility 57 0.070
162
PRS047 Prostatitis 57 0.070
163
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 41 0.070
164
ALL014 Allergic Encephalomyelitis 40 0.070
165
PRP027 Peripheral Vascular Disease 72 0.065
166
P SLP006 Sleep Apnea 71 0.065
167
P PLM037 Pulmonary Hypertension 69 0.065
168
P HPT021 Hepatitis 69 0.065
169
c MCR129 Microvascular Complications of Diabetes 1 67 0.065
170
LVR012 Liver Cirrhosis 67 0.065
171
ALL026 Allergic Hypersensitivity Disease 65 0.065
172
SKN016 Skin Disease 64 0.065
173
KHL003 Kohlschutter-Tonz Syndrome 63 0.065
174
c HPT016 Hepatitis B 63 0.065
175
c ATM011 Autoimmune Hepatitis 63 0.065
176
MCR013 Microphthalmia 62 0.065
177
c PNS012 Paine Syndrome 61 0.065
178
BND020 Bone Disease 60 0.065
179
END030 End Stage Renal Failure 60 0.065
180
P SZR006 Seizure Disorder 59 0.065
181
P GLM007 Glomerulonephritis 58 0.065
182
VSL002 Visual Epilepsy 58 0.065
183
HPT022 Hepatoblastoma 58 0.065
184
P MTC069 Mitochondrial Disorders 57 0.065
185
P CHN012 Chondrosarcoma 57 0.065
186
c VRL010 Viral Hepatitis 56 0.065
187
DBT010 Diabetic Neuropathy 56 0.065
188
P ART021 Arteriosclerosis 56 0.065
189
P CHR345 Chronic Pain 52 0.065
190
PRP080 Peripheral Artery Disease 51 0.065
191
ATX019 Ataxia with Vitamin E Deficiency 46 0.065
192
c MCR112 Microvascular Complications of Diabetes 2 42 0.065
193
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.065
194
c PLY105 Polycystic Ovary Syndrome 1 38 0.065
195
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.065
196
CYS001 Cystic Fibrosis 84 0.060
197
ANX010 Anxiety 75 0.060
198
ACR006 Aceruloplasminemia 74 0.060
199
c ATS007 Autism Spectrum Disorder 69 0.060
200
P ATR011 Atrial Fibrillation 67 0.060
201
GST040 Gastric Adenocarcinoma 67 0.060
202
P PLM036 Pulmonary Fibrosis 66 0.060
203
P HRP006 Herpes Simplex 66 0.060
204
P FRD012 Friedreich Ataxia 1 65 0.060
205
IDP011 Idiopathic Interstitial Pneumonia 65 0.060
206
P MYP004 Myopathy 63 0.060
207
ADL002 Adult Syndrome 62 0.060
208
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.060
209
STT001 Status Epilepticus 61 0.060
210
VTR013 Vitreoretinopathy, Neovascular Inflammatory 61 0.060
211
INS001 Insulinoma 60 0.060
212
c MST023 Mesothelioma, Malignant 59 0.060
213
P FBR017 Fibrosarcoma 57 0.060
214
ENH001 Enhanced S-Cone Syndrome 56 0.060
215
HMS001 Hemosiderosis 54 0.060
216
CLN045 Colonic Benign Neoplasm 52 0.060
217
HYP081 Hypolipoproteinemia 51 0.060
218
CLR109 Colorectal Adenocarcinoma 51 0.060
219
GLS018 Glass Syndrome 51 0.060
220
TST044 Testicular Torsion 49 0.060
221
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 49 0.060
222
P TCL004 T-Cell Leukemia 48 0.060
223
HYP043 Hyperandrogenism 48 0.060
224
VTR007 Vitreoretinopathy 48 0.060
225
URT010 Ureteral Obstruction 46 0.060
226
ORL015 Oral Squamous Cell Carcinoma 44 0.060
227
P RRH023 Rare Hereditary Hemochromatosis 41 0.060
228
c LKM005 Leukemia, T-Cell, Chronic 35 0.060
229
P RHM011 Rheumatoid Arthritis 82 0.055
230
DFC004 Deficiency Anemia 77 0.055
231
P RSP003 Respiratory Failure 75 0.055
232
CRH001 Crohn's Disease 75 0.055
233
END057 Endometrial Cancer 74 0.055
234
P FML011 Familial Adenomatous Polyposis 73 0.055
235
P PHC003 Pheochromocytoma 71 0.055
236
ART016 Aortic Aneurysm 71 0.055
237
LYM133 Lymphoma, Hodgkin, Classic 70 0.055
238
P LYM118 Lymphoma 70 0.055
239
CHL065 Cholangiocarcinoma 68 0.055
240
HYP056 Hypoglycemia 68 0.055
241
LYM007 Lymphangioleiomyomatosis 67 0.055
242
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.055
243
DRM006 Dermatitis 63 0.055
244
OVR029 Ovarian Hyperstimulation Syndrome 63 0.055
245
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.055
246
P CTR002 Cataract 62 0.055
247
CHL123 Chlamydia 60 0.055
248
P MYC008 Myocarditis 60 0.055
249
MNT002 Mental Depression 60 0.055
250
c HPT003 Hepatitis a 60 0.055
251
HPT019 Hepatic Encephalopathy 60 0.055
252
P BRS044 Breast Adenocarcinoma 59 0.055
253
P BNC003 Bone Cancer 56 0.055
254
CMR002 Coumarin Resistance 56 0.055
255
P RTN016 Retinal Degeneration 56 0.055
256
INT079 Intrahepatic Cholangiocarcinoma 54 0.055
257
c ACT020 Acute T Cell Leukemia 54 0.055
258
HMC014 Homocysteinemia 54 0.055
259
SPP010 Suppressor of Tumorigenicity 3 54 0.055
260
c HPT007 Hepatitis E 53 0.055
261
HYP014 Hyperuricemia 52 0.055
262
ADR040 Adrenal Gland Pheochromocytoma 51 0.055
263
PRD004 Prediabetes Syndrome 49 0.055
264
GLC008 Glucose Metabolism Disease 47 0.055
265
HPT004 Hepatic Coma 42 0.055
266
P CLL020 Collagenopathy Type 2 Alpha 1 25 0.055
267
c LKM071 Leukemia, Chronic Lymphocytic 81 0.049
268
BRN028 Brain Cancer 75 0.049
269
c HPT073 Hepatitis C Virus 74 0.049
270
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.049
271
P MLT020 Multiple Sclerosis 73 0.049
272
LPT014 Leptin Deficiency or Dysfunction 72 0.049
273
P AMY004 Amyloidosis 71 0.049
274
P HYP086 Hypothyroidism 70 0.049
275
BRK010 Burkitt Lymphoma 68 0.049
276
P DRM053 Dermatitis, Atopic 68 0.049
277
PRT036 Peritonitis 66 0.049
278
ANG054 Angina Pectoris 66 0.049
279
MSC007 Muscle Hypertrophy 65 0.049
280
P PRP019 Peripheral Nervous System Disease 64 0.049
281
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.049
282
P NRN021 Neuronal Ceroid Lipofuscinosis 63 0.049
283
TXC005 Toxic Shock Syndrome 63 0.049
284
P RHB003 Rhabdomyosarcoma 62 0.049
285
P THL005 Thalassemia 62 0.049
286
c HPT001 Hepatitis C 62 0.049
287
P TXP001 Toxoplasmosis 61 0.049
288
NTR005 Nutritional Deficiency Disease 61 0.049
289
P PLY014 Polycystic Kidney Disease 61 0.049
290
P KDN017 Kidney Cancer 60 0.049
291
c ACT073 Acute Leukemia 59 0.049
292
c ACT075 Acute Myocardial Infarction 59 0.049
293
CHL014 Cholera 58 0.049
294
P SLP005 Sleep Disorder 58 0.049
295
P GST044 Gastritis 58 0.049
296
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.049
297
BCT022 Bacterial Infectious Disease 57 0.049
298
ALL006 Allergic Asthma 56 0.049
299
PPL022 Papilloma 56 0.049
300
c PRD040 Periodontitis, Chronic 56 0.049
301
P DRR001 Diarrhea 55 0.049
302
P RCT021 Rectum Cancer 54 0.049
303
PLM017 Pulmonary Alveolar Microlithiasis 54 0.049
304
P RTN018 Retinal Disease 53 0.049
305
RTN003 Retinal Ischemia 52 0.049
306
P MNC007 Monocytic Leukemia 52 0.049
307
PRS021 Prostatic Adenoma 52 0.049
308
SQM002 Squamous Cell Papilloma 49 0.049
309
47X002 47,xyy 49 0.049
310
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.049
311
TST015 Testicular Disease 49 0.049
312
c MLG068 Malignant Glioma 46 0.049
313
PRM329 Premature Aging 41 0.049
314
HRN029 Hearing Loss, Noise-Induced 38 0.049
315
HRW001 Hair Whorl 36 0.049
316
c LKM004 Leukemia, B-Cell, Chronic 35 0.049
317
CYT018 Cytochrome P450 2d6 Variant 28 0.049
318
c SYS001 Systemic Lupus Erythematosus 88 0.043
319
c DLT002 Dilated Cardiomyopathy 81 0.043
320
c FNC027 Fanconi Anemia, Complementation Group a 81 0.043
321
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.043
322
P EPL164 Epilepsy 73 0.043
323
c HMC039 Hemochromatosis, Type 1 73 0.043
324
P CRD119 Cardiac Arrest 71 0.043
325
c PRM196 Premature Ovarian Failure 1 70 0.043
326
RCK004 Rickets 70 0.043
327
DWN001 Down Syndrome 70 0.043
328
PNC129 Pancreatic Adenocarcinoma 69 0.043
329
PSY004 Psychotic Disorder 68 0.043
330
P FLL037 Follicular Lymphoma 67 0.043
331
PRT037 Pertussis 66 0.043
332
DSS008 Disease of Mental Health 66 0.043
333
ACH004 Achondroplasia 66 0.043
334
HTC003 Hutchinson-Gilford Progeria Syndrome 64 0.043
335
c FNC043 Fanconi Anemia, Complementation Group E 64 0.043
336
LSH001 Leishmaniasis 64 0.043
337
P PSR002 Psoriasis 63 0.043
338
P LPS004 Lupus Erythematosus 62 0.043
339
P HYP750 Hypertriglyceridemia, Familial 62 0.043
340
c ART138 Aortic Aneurysm, Familial Abdominal, 1 62 0.043
341
ACH043 Achondroplasia, Severe, with Developmental Delay and Acanthosis Nigricans 62 0.043
342
P INT143 Interstitial Cystitis 62 0.043
343
CRD223 Cardiac Arrhythmia 61 0.043
344
PTT048 Pituitary Adenoma, Prolactin-Secreting 61 0.043
345
ANR040 Aneurysm 60 0.043
346
c ACT071 Acute Kidney Failure 60 0.043
347
PST028 Post-Traumatic Stress Disorder 60 0.043
348
c ADL017 Adult T-Cell Leukemia 59 0.043
349
CNT047 Contact Dermatitis 58 0.043
350
IRN002 Iron Metabolism Disease 58 0.043
351
THR024 Thrombosis 58 0.043
352
P DNG005 Dengue Virus 57 0.043
353
CMM005 Common Cold 57 0.043
354
GST050 Gastrointestinal System Disease 57 0.043
355
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 57 0.043
356
BRN056 Bronchopulmonary Dysplasia 57 0.043
357
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.043
358
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.043
359
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.043
360
PLM010 Pulmonary Edema 56 0.043
361
PSD012 Pseudoachondroplasia 55 0.043
362
END040 Endogenous Depression 55 0.043
363
PRS045 Prostatic Hypertrophy 55 0.043
364
DMY004 Demyelinating Disease 54 0.043
365
c LRG017 Large Intestine Cancer 53 0.043
366
P TMP001 Temporal Lobe Epilepsy 53 0.043
367
NRT001 Neurotic Disorder 53 0.043
368
P AST007 Astrocytoma 52 0.043
369
AZS001 Azoospermia 51 0.043
370
PST011 Pustulosis of Palm and Sole 51 0.043
371
MTC005 Mitochondrial Metabolism Disease 50 0.043
372
PRS129 Prostatic Hyperplasia, Benign 49 0.043
373
NTR046 Neutrophil Migration 49 0.043
374
RTN020 Retinal Vascular Disease 49 0.043
375
LNG015 Lingual-Facial-Buccal Dyskinesia 48 0.043
376
c HRD026 Hereditary Ataxia 47 0.043
377
P RNL015 Renal Hypertension 47 0.043
378
LWC001 Low Compliance Bladder 45 0.043
379
CRB090 Cerebral Hypoxia 45 0.043
380
KHN001 Kuhnt-Junius Degeneration 45 0.043
381
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 44 0.043
382
P KLZ004 Kala-Azar 1 43 0.043
383
ACT084 Acute Stress Disorder 42 0.043
384
WLL004 Wallerian Degeneration 40 0.043
385
OVR094 Ovarian Epithelial Cancer 39 0.043
386
CHL147 Chlamydia Pneumonia 39 0.043
387
PRS011 Persian Gulf Syndrome 37 0.043
388
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.043
389
P VSC018 Visceral Steatosis 34 0.043
390
c DNT047 Dentinogenesis Imperfecta Type 2 34 0.043
391
DMN026 Dementia Pugilistica 28 0.043
392
PRX085 Preaxial Hallucal Polydactyly 27 0.043
393
ESP021 Esophageal Cancer 90 0.035
394
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.035
395
P SCH015 Schizophrenia 76 0.035
396
MRF001 Marfan Syndrome 75 0.035
397
c THR092 Thrombophilia Due to Thrombin Defect 74 0.035
398
c TBR025 Tuberous Sclerosis 1 74 0.035
399
P TBR001 Tuberous Sclerosis 72 0.035
400
P ART022 Arthritis 71 0.035
401
P PNM007 Pneumonia 71 0.035
402
c EXD008 Exudative Vitreoretinopathy 1 69 0.035
403
KRT019 Keratitis, Hereditary 69 0.035
404
P LNG028 Long Qt Syndrome 68 0.035
405
WRN001 Werner Syndrome 68 0.035
406
SKN019 Skin Melanoma 68 0.035
407
ADR054 Adrenocortical Carcinoma, Hereditary 68 0.035
408
SRC014 Sarcoma 67 0.035
409
CLF027 Cleft Palate, Isolated 67 0.035
410
P THR014 Thrombocytopenia 67 0.035
411
P MNN013 Meningitis 67 0.035
412
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.035
413
CHG001 Chagas Disease 66 0.035
414
P SPN046 Spinal Muscular Atrophy 65 0.035
415
c GCH015 Gaucher Disease, Type I 65 0.035
416
P NPH012 Nephrotic Syndrome 65 0.035
417
IRR002 Irritable Bowel Syndrome 65 0.035
418
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.035
419
P VSC011 Vasculitis 64 0.035
420
KRN002 Kearns-Sayre Syndrome 64 0.035
421
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.035
422
APN008 Apnea, Obstructive Sleep 64 0.035
423
P GCH001 Gaucher's Disease 63 0.035
424
c GLC092 Glaucoma, Primary Open Angle 63 0.035
425
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 63 0.035
426
OST003 Osteonecrosis 62 0.035
427
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 62 0.035
428
CRN296 Carnitine Palmitoyltransferase Ii Deficiency, Infantile 62 0.035
429
TTN003 Tetanus 62 0.035
430
THY121 Thyroid Gland Anaplastic Carcinoma 62 0.035
431
CRY035 Cryptorchidism, Unilateral or Bilateral 61 0.035
432
ACQ007 Acquired Immunodeficiency Syndrome 61 0.035
433
P MCH002 Machado-Joseph Disease 61 0.035
434
DPH001 Diphtheria 61 0.035
435
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.035
436
NRN004 Neuroendocrine Tumor 59 0.035
437
P BPL003 Bipolar Disorder 59 0.035
438
CNS004 Constipation 59 0.035
439
TRD006 Tardive Dyskinesia 58 0.035
440
P ALC033 Alcohol Use Disorder 58 0.035
441
ERY051 Erythroleukemia, Familial 58 0.035
442
TRG002 Trigeminal Neuralgia 58 0.035
443
P MMP001 Mumps 57 0.035
444
P PRN023 Prion Disease 57 0.035
445
SPN035 Spindle Cell Sarcoma 57 0.035
446
RHM027 Rheumatic Disease 56 0.035
447
c BCT007 Bacterial Meningitis 56 0.035
448
P PLY018 Polycythemia 56 0.035
449
c SVR001 Severe Acute Respiratory Syndrome 56 0.035
450
c FNC042 Fanconi Anemia, Complementation Group D2 56 0.035
451
PHR003 Pharyngitis 56 0.035
452
DFF005 Diffuse Large B-Cell Lymphoma 56 0.035
453
SYN007 Synovitis 55 0.035
454
P TCD001 Tic Disorder 55 0.035
455
P TRM003 Tremor 55 0.035
456
HMT018 Hematopoietic Stem Cell Transplantation 54 0.035
457
PRP016 Paraplegia 54 0.035
458
MSC190 Muscular Disease 54 0.035
459
P ACT105 Acute Mountain Sickness 53 0.035
460
CHC001 Chickenpox 53 0.035
461
P PTT006 Pituitary Adenoma 53 0.035
462
P MTC133 Mitochondrial Myopathy 53 0.035
463
c ACT134 Acute Liver Failure 53 0.035
464
c HYP841 Hypoalphalipoproteinemia, Primary, 1 53 0.035
465
GST023 Gastric Ulcer 53 0.035
466
SKN022 Skin Squamous Cell Carcinoma 53 0.035
467
FDL002 Food Allergy 52 0.035
468
LMY002 Leiomyoma 52 0.035
469
OCL006 Ocular Hypertension 52 0.035
470
KRT009 Keratosis 52 0.035
471
RDC002 Radiculopathy 51 0.035
472
PLC008 Placenta Disease 51 0.035
473
VRC001 Varicocele 51 0.035
474
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.035
475
ADR016 Adrenal Cortical Carcinoma 51 0.035
476
LMB062 Limb Ischemia 50 0.035
477
P ACT008 Actinic Keratosis 50 0.035
478
c FLL041 Follicular Lymphoma 1 50 0.035
479
P OPN001 Open-Angle Glaucoma 50 0.035
480
MCR004 Macroglobulinemia 50 0.035
481
P INT099 Intrahepatic Cholestasis of Pregnancy 50 0.035
482
c HYP768 Hyperlipoproteinemia, Type I 50 0.035
483
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 49 0.035
484
END062 Endometrial Hyperplasia 49 0.035
485
P OBS001 Obstructive Jaundice 49 0.035
486
P CRV031 Cervical Adenocarcinoma 49 0.035
487
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.035
488
HYP781 Hypoascorbemia 48 0.035
489
LYM019 Lymphosarcoma 48 0.035
490
ANV001 Anovulation 47 0.035
491
HMP009 Haemophilus Influenzae 46 0.035
492
CTS005 Catastrophic Antiphospholipid Syndrome 44 0.035
493
TNG009 Tongue Squamous Cell Carcinoma 44 0.035
494
ADR004 Adrenal Cortical Adenocarcinoma 44 0.035
495
ACT003 Acute Kidney Tubular Necrosis 42 0.035
496
DBT007 Diabetic Cataract 42 0.035
497
c MJR024 Major Affective Disorder 9 42 0.035
498
c SPR086 Spermatogenic Failure 3 41 0.035
499
SKN005 Skin Atrophy 41 0.035
500
HYP540 Hypertension, Diastolic 41 0.035
501
KLD004 Keloid Disorder 41 0.035
502
ORC001 Orchitis 41 0.035
503
IMM001 Immune-Complex Glomerulonephritis 40 0.035
504
c MJR022 Major Affective Disorder 8 39 0.035
505
CNT017 Central Nervous System Origin Vertigo 38 0.035
506
SYS071 Systemic Autoimmune Disease 38 0.035
507
c PRK085 Parkinson Disease 1, Autosomal Dominant 37 0.035
508
SCR003 Secretory Diarrhea 36 0.035
509
LMN011 Laminopathy 34 0.035
510
RRS014 Rare Surgical Neurologic Disease 33 0.035
511
PLY150 Polykaryocytosis Inducer 31 0.035
512
SKN020 Skin Papilloma 31 0.035
513
DBT081 Diabetic Encephalopathy 30 0.035
514
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 29 0.035
515
c PRK091 Parkinson Disease 4, Autosomal Dominant 27 0.035
516
c CLB022 Coloboma, Ocular, Autosomal Recessive 27 0.035
517
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 25 0.035
518
NRL016 Neural Tube Defects 83 0.025
519
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.025
520
AST005 Asthma 80 0.025
521
PFF001 Pfeiffer Syndrome 79 0.025
522
c CWD006 Cowden Syndrome 1 76 0.025
523
KPS004 Kaposi Sarcoma 75 0.025
524
SCK003 Sickle Cell Anemia 74 0.025
525
HMN044 Human Immunodeficiency Virus Type 1 73 0.025
526
c BTT014 Beta-Thalassemia 73 0.025
527
MYL009 Myelodysplastic Syndrome 72 0.025
528
P LFR001 Li-Fraumeni Syndrome 71 0.025
529
BRT054 Brittle Bone Disorder 71 0.025
530
P NJM001 Nijmegen Breakage Syndrome 70 0.025
531
PLY001 Polycythemia Vera 70 0.025
532
BRN024 Bronchitis 70 0.025
533
FRN006 Frontotemporal Dementia 70 0.025
534
c WLM013 Wilms Tumor 1 69 0.025
535
MNT001 Mantle Cell Lymphoma 69 0.025
536
CRB037 Cerebral Palsy 69 0.025
537
P INF038 Influenza 69 0.025
538
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.025
539
P ORT004 Orthostatic Intolerance 68 0.025
540
ALC007 Alcohol Dependence 68 0.025
541
c BSL007 Basal Cell Carcinoma 68 0.025
542
c HRD010 Hereditary Spastic Paraplegia 67 0.025
543
P HYP098 Hypereosinophilic Syndrome 67 0.025
544
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.025
545
c ART101 Aortic Valve Disease 2 67 0.025
546
P BRD002 Bardet-Biedl Syndrome 66 0.025
547
P MTR014 Motor Neuron Disease 66 0.025
548
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 65 0.025
549
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.025
550
OST017 Osteomyelitis 65 0.025
551
KWS002 Kawasaki Disease 65 0.025
552
FCT007 Factor Vii Deficiency 65 0.025
553
CLR108 Colorectal Adenoma 64 0.025
554
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 64 0.025
555
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 64 0.025
556
END041 Endometrial Adenocarcinoma 64 0.025
557
P THY023 Thymoma 64 0.025
558
P FCL005 Focal Segmental Glomerulosclerosis 63 0.025
559
MDD011 Mood Disorder 62 0.025
560
MRK001 Merkel Cell Carcinoma 62 0.025
561
P ESP024 Esophagitis 62 0.025
562
PRP083 Porphyria, Acute Intermittent 62 0.025
563
BRC012 Brucellosis 62 0.025
564
P MCP040 Mucopolysaccharidosis-Plus Syndrome 62 0.025
565
RHB001 Rhabdoid Cancer 62 0.025
566
P ANP001 Anaplastic Large Cell Lymphoma 62 0.025
567
INT066 Interstitial Lung Disease 61 0.025
568
PRT013 Portal Hypertension 61 0.025
569
CTN007 Cutaneous Leishmaniasis 61 0.025
570
CHR066 Chronic Fatigue Syndrome 61 0.025
571
TKY002 Takayasu Arteritis 61 0.025
572
HLC007 Helicobacter Pylori Infection 61 0.025
573
P CRD132 Cardiac Conduction Defect 61 0.025
574
P CND004 Candidiasis 61 0.025
575
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 61 0.025
576
GNG013 Gingivitis 60 0.025
577
c LPM012 Lipomatosis, Multiple 60 0.025
578
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.025
579
FBR047 Fibromyalgia 60 0.025
580
ATY005 Atypical Teratoid Rhabdoid Tumor 60 0.025
581
BRN002 Bronchiolitis 60 0.025
582
P GLL020 Gallbladder Disease 60 0.025
583
P CYS018 Cystitis 59 0.025
584
c THY102 Thyroid Cancer, Nonmedullary, 2 59 0.025
585
ANG020 Angiosarcoma 59 0.025
586
c CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 59 0.025
587
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 59 0.025
588
P PGT001 Paget's Disease of Bone 59 0.025
589
P MLN069 Melanoma, Uveal 59 0.025
590
P LRY044 Larynx Cancer 59 0.025
591
P PRP029 Porphyria 58 0.025
592
P UVT001 Uveitis 58 0.025
593
P SLV026 Salivary Gland Carcinoma 58 0.025
594
CRV038 Cervical Squamous Cell Carcinoma 58 0.025
595
HYD002 Hydronephrosis 58 0.025
596
c THY109 Thyroid Cancer, Nonmedullary, 1 58 0.025
597
SCH014 Schistosomiasis 57 0.025
598
LMY014 Leiomyoma, Uterine 57 0.025
599
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 57 0.025
600
P ORL007 Oral Cavity Cancer 57 0.025
601
GLL018 Gallbladder Cancer 57 0.025
602
HMG005 Hemoglobinopathy 57 0.025
603
c SPS222 Spastic Paraplegia 20, Autosomal Recessive 57 0.025
604
HRY003 Hairy Cell Leukemia 57 0.025
605
SFT003 Soft Tissue Sarcoma 57 0.025
606
ERY003 Erythema Multiforme 57 0.025
607
PRP030 Purpura 56 0.025
608
ALL010 Allergic Contact Dermatitis 56 0.025
609
APH001 Aphthous Stomatitis 56 0.025
610
c SPS215 Spastic Paraplegia 3, Autosomal Dominant 56 0.025
611
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.025
612
c BRD014 Bardet-Biedl Syndrome 2 56 0.025
613
P RBL001 Rubella 56 0.025
614
ALV005 Alveolar Soft Part Sarcoma 56 0.025
615
P FTL001 Fetal Alcohol Syndrome 56 0.025
616
MCS002 Mucositis 56 0.025
617
MTH009 Mouth Disease 56 0.025
618
CNV004 Canavan Disease 56 0.025
619
AVN001 Avian Influenza 56 0.025
620
P PLM034 Pulmonary Emphysema 55 0.025
621
AMN003 Amnestic Disorder 55 0.025
622
c THY107 Thymoma, Familial 55 0.025
623
MST005 Mastitis 55 0.025
624
P LCH002 Lichen Planus 55 0.025
625
P ICH004 Ichthyosis 55 0.025
626
P HYP076 Hyperthyroidism 55 0.025
627
ADN027 Adenomyosis 55 0.025
628
P PLY019 Polyneuropathy 55 0.025
629
P NRV006 Nervous System Cancer 55 0.025
630
PRN019 Perinatal Necrotizing Enterocolitis 55 0.025
631
P OPT009 Optic Neuritis 55 0.025
632
P OVR049 Ovarian Disease 55 0.025
633
PRM042 Primary Effusion Lymphoma 55 0.025
634
ORL004 Oral Submucous Fibrosis 55 0.025
635
SML019 Smallpox 55 0.025
636
THY124 Thyroid Gland Papillary Carcinoma 54 0.025
637
P MMB011 Membranous Nephropathy 54 0.025
638
INT075 Intracranial Hypertension 54 0.025
639
P TYR004 Tyrosinemia 54 0.025
640
PNC001 Pancytopenia 54 0.025
641
CLR030 Clear Cell Renal Cell Carcinoma 54 0.025
642
AMN001 Amenorrhea 54 0.025
643
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 54 0.025
644
P SLM003 Salmonellosis 54 0.025
645
P PTS002 Ptosis 53 0.025
646
DFF036 Differentiated Thyroid Carcinoma 53 0.025
647
c SPN393 Spinal Muscular Atrophy, Type I 53 0.025
648
P ECL001 Eclampsia 53 0.025
649
P SCK005 Sickle Cell Disease 53 0.025
650
THY123 Thyroid Gland Follicular Carcinoma 52 0.025
651
CHR073 Choreatic Disease 52 0.025
652
NPH003 Nephrocalcinosis 52 0.025
653
LYS002 Lysosomal Storage Disease 52 0.025
654
CRV040 Cervix Carcinoma 52 0.025
655
PNG002 Pain Agnosia 52 0.025
656
P EMB005 Embryonal Rhabdomyosarcoma 52 0.025
657
THR004 Thrombocytosis 52 0.025
658
MYM001 Myoma 52 0.025
659
NRT004 Neuritis 52 0.025
660
P TRT010 Teratoma 52 0.025
661
MCL006 Macular Retinal Edema 52 0.025
662
P MYT002 Myotonic Dystrophy 52 0.025
663
c CNG021 Congenital Toxoplasmosis 52 0.025
664
c CNT033 Central Nervous System Cancer 51 0.025
665
STM007 Stomatitis 51 0.025
666
DYS014 Dyspepsia 51 0.025
667
c MLG054 Malignant Histiocytosis 51 0.025
668
OVR082 Overgrowth Syndrome 51 0.025
669
ENT011 Enterocolitis 51 0.025
670
c OPT053 Optic Atrophy 1 51 0.025
671
HYP080 Hypogonadism 51 0.025
672
URM002 Uremia 50 0.025
673
VCC001 Vaccinia 50 0.025
674
ILT001 Ileitis 50 0.025
675
PRT018 Portal Vein Thrombosis 50 0.025
676
BLD044 Bladder Disease 50 0.025
677
IGG001 Iga Glomerulonephritis 50 0.025
678
c HMN021 Human T-Cell Leukemia Virus Type 1 50 0.025
679
PLR008 Pleurisy 50 0.025
680
MNN009 Meningoencephalitis 50 0.025
681
P LPM005 Lipomatosis 49 0.025
682
GST049 Gastrointestinal System Cancer 49 0.025
683
RYS001 Reye Syndrome 49 0.025
684
HYP006 Hypertensive Heart Disease 49 0.025
685
P RNV001 Renovascular Hypertension 49 0.025
686
THY128 Thyroid Tumor 49 0.025
687
P ART106 Arterial Calcification, Generalized, of Infancy, 1 49 0.025
688
P HMN032 Human Herpesvirus 8 49 0.025
689
SKN013 Skin Benign Neoplasm 49 0.025
690
P END046 Endometritis 49 0.025
691
MTB004 Metabolic Acidosis 48 0.025
692
CRN027 Corneal Neovascularization 48 0.025
693
PRS034 Parasitic Helminthiasis Infectious Disease 48 0.025
694
VRL003 Variola Major 48 0.025
695
P FNC004 Fanconi Syndrome 48 0.025
696
NRN001 Neuroendocrine Carcinoma 48 0.025
697
c CRD065 Cardiomyopathy, Familial Hypertrophic, 2 48 0.025
698
DRG003 Drug Dependence 48 0.025
699
c PRM093 Premature Ovarian Failure 7 48 0.025
700
TTR011 Tetraploidy 47 0.025
701
PTT037 Pituitary Tumors 47 0.025
702
PPT001 Peptic Esophagitis 47 0.025
703
P SMP003 Simpson-Golabi-Behmel Syndrome 47 0.025
704
HDN002 Head Injury 47 0.025
705
TRC023 Trichinosis 47 0.025
706
P MTH007 Methemoglobinemia 47 0.025
707
MCL027 Macular Dystrophy, Dominant Cystoid 47 0.025
708
ART004 Aortic Atherosclerosis 47 0.025
709
IRR003 Irritant Dermatitis 46 0.025
710
PLL012 Pollen Allergy 46 0.025
711
DBT006 Diabetic Macular Edema 46 0.025
712
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.025
713
P KRT005 Keratoacanthoma 46 0.025
714
HLX001 Helix Syndrome 46 0.025
715
TRC003 Trichomoniasis 46 0.025
716
EXS001 Exostosis 46 0.025
717
SYN005 Synostosis 46 0.025
718
PNM013 Pneumococcal Meningitis 45 0.025
719
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.025
720
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 45 0.025
721
NWC001 Newcastle Disease 45 0.025
722
c DYS119 Dystonia 9 45 0.025
723
PGM003 Pigmentation Disease 45 0.025
724
c FTL006 Fetal Alcohol Spectrum Disorder 45 0.025
725
IDP033 Idiopathic Edema 44 0.025
726
c HYP272 Hypercholesterolemia, Familial, 3 44 0.025
727
RTR008 Root Resorption 44 0.025
728
CHD004 Chudley-Mccullough Syndrome 44 0.025
729
BRN032 Brain Glioma 44 0.025
730
MTC004 Mitochondrial Encephalomyopathy 44 0.025
731
BNS007 Bone Sarcoma 44 0.025
732
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.025
733
c MLG079 Malignant Pleural Mesothelioma 43 0.025
734
LKS001 Leukostasis 43 0.025
735
DST006 Diastolic Heart Failure 43 0.025
736
GST071 Gastrointestinal Carcinoma 42 0.025
737
PRS042 Prostate Disease 42 0.025
738
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.025
739
ASP030 Aspirin Resistance 42 0.025
740
P GLM044 Glomerular Disease 42 0.025
741
TRP009 Triple X Syndrome 42 0.025
742
c LFR007 Li-Fraumeni Syndrome 2 41 0.025
743
SNL007 Senile Cataract 41 0.025
744
PLM005 Pleomorphic Lipoma 41 0.025
745
PLY100 Polyploidy 41 0.025
746
DYS030 Dysferlinopathy 41 0.025
747
MYF001 Myofibroma 40 0.025
748
MST004 Mast Cell Neoplasm 40 0.025
749
UTR043 Uterine Sarcoma 40 0.025
750
MNK002 Monkeypox 40 0.025
752
ANG002 Angiostrongyliasis 40 0.025
753
OST115 Osteonecrosis of the Jaw 40 0.025
754
HST016 Histiocytic Sarcoma 40 0.025
755
FST001 Foster-Kennedy Syndrome 40 0.025
756
HYP064 Hypogonadotropism 40 0.025
757
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 40 0.025
758
HMR023 Hemorrhagic Cystitis 40 0.025
759
c ATM075 Autoimmune Encephalitis 39 0.025
760
EXT007 Extracutaneous Mastocytoma 39 0.025
761
SPS057 Spasticity 38 0.025
763
c ERL056 Early-Onset Parkinson's Disease 38 0.025
764
KLD003 Keloid Formation 38 0.025
765
ACY011 Acyl-Coa Dehydrogenase Deficiency 38 0.025
766
MNN017 Mononeuropathy 38 0.025
767
BCK003 Background Diabetic Retinopathy 37 0.025
768
SCR011 Scrapie 37 0.025
769
EXT048 Extranodal Nasal Nk/t Cell Lymphoma 37 0.025
770
c ATM022 Autoimmune Myocarditis 36 0.025
771
CHN002 Chancroid 36 0.025
772
c PRG021 Paragangliomas 4 36 0.025
773
PLM135 Palmoplantar Keratoderma, Bothnian Type 35 0.025
774
END011 Endometriosis of Ovary 35 0.025
775
GNT167 Genetic Obesity 35 0.025
776
DXR001 Doxorubicin Induced Cardiomyopathy 34 0.025
777
BWN006 Bowen's Disease 34 0.025
778
DFF015 Diffuse Glomerulonephritis 33 0.025
779
c FTL070 Fetal Akinesia Deformation Sequence 2 33 0.025
780
P SKN067 Skin/hair/eye Pigmentation, Variation in, 2 32 0.025
781
STT009 Sutton Disease 2 31 0.025
782
c SPS036 Spastic Paraplegia 3 31 0.025
783
P GST047 Gastrointestinal Neuroendocrine Tumor 30 0.025
784
c HRD138 Hereditary Motor and Sensory Neuropathy V 29 0.025
785
MNG007 Manganese Poisoning 28 0.025
786
QLT008 Qualitative or Quantitative Defects of Dysferlin 28 0.025
787
MST020 Mast Cell Activation Syndrome 28 0.025
788
KDN013 Kidney Hypertrophy 27 0.025
789
P PRG139 Progeroid Syndrome 27 0.025
790
CRT084 Creatinine Clearance Quantitative Trait Locus 26 0.025
791
MYT026 Myotonia Atrophica 25 0.025
792
c PRM243 Primary Bone Cancer 25 0.025
793
DFF023 Diffuse Palmoplantar Keratoderma, Bothnian Type 14 0.025
Content
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