Search results for srm

602 hits were found for srm

# Family MCID Name MIFTS Score
1
MLR004 Malaria 78 15.019
2
SLP001 Sleeping Sickness 56 14.863
3
CHG001 Chagas Disease 65 14.863
4
LSH001 Leishmaniasis 63 14.863
5
SYN089 Syndromic X-Linked Intellectual Disability Snyder Type 34 8.581
6
THY006 Thymus Lymphoma 27 8.581
7
P KDN017 Kidney Cancer 60 3.008
8
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 2.945
9
P OVR042 Ovarian Cancer 88 1.844
10
OST012 Osteoarthritis 77 1.792
11
RNL114 Renal Cell Carcinoma, Nonpapillary 79 1.683
12
DWN001 Down Syndrome 70 1.624
13
P MLT020 Multiple Sclerosis 79 1.495
14
ANG018 Angiomyolipoma 45 1.472
15
P CLR023 Colorectal Cancer 100 1.429
16
P BLD134 Bladder Cancer 79 1.332
17
P PRS040 Prostate Cancer 95 1.312
18
MTC005 Mitochondrial Metabolism Disease 45 1.293
19
P CRN300 Coronary Heart Disease 1 73 1.272
20
MDD011 Mood Disorder 62 1.226
21
P CHR345 Chronic Pain 50 1.214
22
P RHM011 Rheumatoid Arthritis 81 1.146
23
c SML038 Small Cell Cancer of the Lung 69 1.135
24
P MLN008 Melanoma 75 1.039
25
P NRP001 Neuropathy 59 1.039
26
P ART022 Arthritis 70 1.029
27
LBR038 Leber Hereditary Optic Neuropathy, Modifier of 62 1.020
28
P OPT006 Optic Nerve Disease 57 1.020
29
BNG018 Benign Paroxysmal Positional Nystagmus 40 1.020
30
P HRD217 Hereditary Optic Neuropathy 36 1.020
31
P PNC035 Pancreatic Cancer 86 1.000
32
TRN015 Transient Cerebral Ischemia 62 1.000
33
CRT015 Carotid Artery Occlusion 45 1.000
34
URT010 Ureteral Obstruction 45 0.978
35
P BRS047 Breast Cancer 97 0.955
36
ONC007 Oncocytoma 49 0.955
37
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.955
38
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.955
39
IRN002 Iron Metabolism Disease 56 0.955
40
BCK006 Back Pain 43 0.936
41
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.929
42
CHR178 Chromosomal Triplication 34 0.929
43
WLS001 Wilson Disease 70 0.899
44
P HRD144 Hereditary Mixed Polyposis Syndrome 54 0.899
45
BCT022 Bacterial Infectious Disease 56 0.899
46
BRN032 Brain Glioma 45 0.899
47
CHL065 Cholangiocarcinoma 58 0.899
48
INT079 Intrahepatic Cholangiocarcinoma 51 0.899
49
P ART021 Arteriosclerosis 53 0.899
50
P STR020 Strabismus 56 0.875
51
MCH006 Mechanical Strabismus 40 0.875
52
INS024 Insulin-Like Growth Factor I 77 0.864
53
ATM095 Autoimmune Disease 61 0.864
54
P LNG064 Lung Cancer Susceptibility 3 70 0.864
55
LVR012 Liver Cirrhosis 62 0.864
56
P RCT021 Rectum Cancer 54 0.864
57
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 0.864
58
P RHB003 Rhabdomyosarcoma 66 0.818
59
CRB037 Cerebral Palsy 67 0.788
60
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.773
61
c PRG018 Paragangliomas 1 59 0.773
62
P PRG013 Paraganglioma 57 0.773
63
P CRV039 Cervicitis 52 0.773
64
HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 61 0.773
65
STR067 Stroke, Ischemic 79 0.715
66
GST019 Gastrointestinal Stromal Tumor 78 0.708
67
P MYP004 Myopathy 67 0.706
68
P ATR011 Atrial Fibrillation 66 0.698
69
P CRP001 Carpal Tunnel Syndrome 66 0.698
70
PSR001 Psoriatic Arthritis 61 0.652
71
CNS004 Constipation 56 0.643
72
SPN186 Spinal Cord Injury 61 0.643
73
P RNL017 Renal Oncocytoma 54 0.634
74
CLR030 Clear Cell Renal Cell Carcinoma 54 0.634
75
SYN007 Synovitis 54 0.624
76
PLC002 Plica Syndrome 35 0.624
77
P PLV020 Pelvic Organ Prolapse 58 0.604
78
48X005 48,xyyy 39 0.604
79
47X002 47,xyy 48 0.604
80
c SPN225 Spondyloarthropathy 1 70 0.584
81
c MJR024 Major Affective Disorder 9 40 0.584
82
c MJR022 Major Affective Disorder 8 37 0.584
83
SPN051 Spondylitis 51 0.584
84
INF009 Inflammatory Spondylopathy 30 0.584
85
P BPL003 Bipolar Disorder 56 0.584
86
END086 End Stage Renal Disease 54 0.584
87
P SCH015 Schizophrenia 74 0.573
88
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.573
89
P VTR007 Vitreoretinopathy 45 0.573
90
CHL068 Cholestasis 61 0.551
91
P TMP001 Temporal Lobe Epilepsy 49 0.551
92
P MSC005 Muscular Dystrophy 66 0.551
93
P ENC018 Encephalopathy 62 0.540
94
END040 Endogenous Depression 54 0.529
95
P ALZ034 Alzheimer Disease 87 0.517
96
P MJR001 Major Depressive Disorder 68 0.517
97
MNT002 Mental Depression 56 0.517
98
MSC157 Muscular Dystrophy, Duchenne Type 79 0.517
99
DPR016 Depression 65 0.517
100
P ATS364 Autism 72 0.505
101
P SNS001 Sensorineural Hearing Loss 59 0.493
102
c JVN010 Juvenile Rheumatoid Arthritis 66 0.493
103
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.481
104
SCR011 Scrapie 39 0.481
105
c ATS007 Autism Spectrum Disorder 72 0.468
106
QDR001 Quadriplegia 49 0.468
107
P DMN002 Dementia 65 0.468
108
P SCL018 Scoliosis 57 0.455
109
IDP070 Idiopathic Scoliosis 41 0.455
110
TNS014 Tenosynovitis 45 0.455
111
OVR094 Ovarian Epithelial Cancer 39 0.427
112
c BRN108 Branchiootic Syndrome 1 63 0.413
113
P SCL057 Scoliosis, Isolated 1 40 0.413
114
MTH071 Methane Production 25 0.413
115
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.413
116
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 52 0.413
117
P EPL164 Epilepsy 70 0.413
118
STT001 Status Epilepticus 58 0.413
119
ENT004 Enthesopathy 51 0.413
120
P SZR006 Seizure Disorder 69 0.413
121
CHR177 Chromophobe Renal Cell Carcinoma 54 0.413
122
P HMR005 Hemorrhoid 49 0.413
124
GST092 Gastroesophageal Reflux 60 0.398
125
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.398
126
c SYS001 Systemic Lupus Erythematosus 86 0.398
127
P ADN016 Adenocarcinoma 63 0.398
128
P LTR001 Lateral Sclerosis 58 0.398
129
c CHR684 Chronic Kidney Disease 74 0.398
130
P LPS004 Lupus Erythematosus 61 0.398
131
PRT251 Proteinuria, Chronic Benign 58 0.382
132
DSS032 Disease by Infectious Agent 55 0.382
133
RTN017 Retinal Detachment 60 0.382
134
SVR004 Severe Combined Immunodeficiency 71 0.382
135
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.366
136
ANX010 Anxiety 70 0.366
137
RNL065 Renal Cell Carcinoma, Papillary, 1 79 0.366
138
IMM167 Immune Deficiency Disease 77 0.366
139
NRL016 Neural Tube Defects 81 0.366
140
AGM019 Agammaglobulinemia, X-Linked 72 0.366
141
P HPT023 Hepatocellular Carcinoma 95 0.366
142
PST028 Post-Traumatic Stress Disorder 59 0.366
143
P AGM001 Agammaglobulinemia 67 0.366
144
PPL002 Papillary Carcinoma 46 0.366
145
SPN009 Spindle Cell Rhabdomyosarcoma 40 0.366
146
CHR176 Chromophil Renal Cell Carcinoma 23 0.366
147
CYS001 Cystic Fibrosis 77 0.349
148
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.349
149
P LYM118 Lymphoma 69 0.349
150
P WSK001 Wiskott-Aldrich Syndrome 72 0.349
151
DSS008 Disease of Mental Health 74 0.349
152
CHL014 Cholera 62 0.349
153
SPN027 Spinal Stenosis 59 0.349
154
c HPT001 Hepatitis C 61 0.349
155
FDL002 Food Allergy 47 0.349
156
P FBR017 Fibrosarcoma 55 0.349
157
ANX004 Anoxia 40 0.349
158
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.349
159
MYL069 Myeloma, Multiple 77 0.331
160
GST105 Gastroesophageal Adenocarcinoma 42 0.331
161
ATH013 Atherosclerosis Susceptibility 63 0.331
162
EXS001 Exostosis 49 0.331
163
P SBS003 Substance Abuse 54 0.331
164
CRB039 Cerebrovascular Disease 65 0.331
165
P MSC003 Muscular Atrophy 52 0.331
166
MTB016 Metabolic Myopathy 30 0.331
167
P CHN012 Chondrosarcoma 56 0.312
168
P GRF003 Graft-Versus-Host Disease 71 0.312
169
P PRK039 Parkinsonism 55 0.312
170
P MYS005 Myositis 56 0.312
171
P OST002 Osteoporosis 77 0.312
172
PNG002 Pain Agnosia 51 0.312
173
ANG020 Angiosarcoma 63 0.312
174
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.312
175
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.312
176
MLT157 Multiple System Atrophy 1 69 0.312
177
P EMB005 Embryonal Rhabdomyosarcoma 53 0.312
178
P PRN023 Prion Disease 60 0.312
179
GNR004 Generalized Anxiety Disorder 55 0.312
180
P THR014 Thrombocytopenia 66 0.312
181
OST159 Osteogenic Sarcoma 66 0.312
182
P NSP012 Nasopharyngeal Carcinoma 60 0.312
183
CYT002 Cytokine Deficiency 43 0.312
184
c TYP009 Type 2 Diabetes Mellitus 92 0.292
185
AGN016 Aging 54 0.292
186
P AST005 Asthma 76 0.292
187
P CHR071 Charcot-Marie-Tooth Disease 64 0.292
188
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 25 0.292
189
LMB062 Limb Ischemia 55 0.292
190
c HPT073 Hepatitis C Virus 71 0.292
191
PPL052 Papillomatosis, Confluent and Reticulated 34 0.292
192
c SCL052 Scleroderma, Familial Progressive 60 0.292
193
GLB002 Glioblastoma 67 0.292
194
P HPT021 Hepatitis 68 0.292
195
P ECL001 Eclampsia 52 0.292
196
TTH006 Tooth Disease 51 0.292
197
P TRM003 Tremor 50 0.292
198
P CTR002 Cataract 59 0.292
199
LNG099 Lung Disease 62 0.292
200
VSC002 Vascular Dementia 59 0.292
201
P INF038 Influenza 68 0.292
202
P BCL017 B-Cell Lymphoma 57 0.292
204
P PRK057 Parkinson Disease, Late-Onset 79 0.270
205
MST021 Meester-Loeys Syndrome 38 0.270
206
SRC014 Sarcoma 64 0.270
207
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.270
208
PRP027 Peripheral Vascular Disease 71 0.270
209
P SPN046 Spinal Muscular Atrophy 62 0.270
210
MTN001 Metanephric Adenoma 39 0.270
211
P LMY004 Leiomyosarcoma 62 0.270
212
c ACT071 Acute Kidney Failure 60 0.270
213
P CHR012 Chronic Granulomatous Disease 69 0.270
214
P SKN015 Skin Carcinoma 71 0.270
215
NRM005 Neuromuscular Disease 63 0.270
216
SPN035 Spindle Cell Sarcoma 51 0.270
217
P NRB001 Neuroblastoma 66 0.270
218
P MYC033 Myoclonus 46 0.270
219
CRH001 Crohn's Disease 80 0.270
220
ADN001 Adenosine Deaminase Deficiency 59 0.270
221
FTT001 Fatty Liver Disease 61 0.270
222
PST021 Postpartum Depression 50 0.270
223
P SRC025 Sarcoidosis 1 70 0.247
224
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.247
225
c HMP029 Hemophilia a 69 0.247
226
RCK004 Rickets 65 0.247
227
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.247
228
INT395 Intracranial Meningioma 48 0.247
229
P DRM010 Dermatomyositis 61 0.247
230
PLY150 Polykaryocytosis Inducer 29 0.247
231
SPN019 Spondylolisthesis 52 0.247
232
APH002 Aphasia 55 0.247
233
ORL015 Oral Squamous Cell Carcinoma 43 0.247
234
P HNT016 Huntington Disease 73 0.247
235
FCT001 Factor Viii Deficiency 62 0.247
236
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 49 0.247
237
GT001 Gout 63 0.247
238
LPD008 Lipid Metabolism Disorder 61 0.247
239
ACQ007 Acquired Immunodeficiency Syndrome 58 0.247
240
c INH020 Inherited Metabolic Disorder 47 0.247
241
P MTR012 Mitral Valve Disease 57 0.247
242
BRN024 Bronchitis 67 0.247
243
MYP002 Myoepithelial Carcinoma 46 0.247
244
ACT084 Acute Stress Disorder 53 0.247
245
P MTR003 Mitral Valve Stenosis 53 0.247
246
SQM006 Squamous Cell Carcinoma 59 0.247
247
SYN005 Synostosis 43 0.247
248
P PYL005 Pyelonephritis 56 0.247
249
LYM017 Lyme Disease 63 0.247
250
c ADL019 Adult Fibrosarcoma 30 0.247
251
MSN004 Mesenchymal Cell Neoplasm 42 0.247
252
PST011 Pustulosis of Palm and Sole 52 0.247
253
MNN043 Meningioma, Familial 79 0.247
254
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.247
255
GLL048 Glial Tumor 52 0.247
256
HYP266 Hypoxia 56 0.247
257
P HMP007 Hemophilia 52 0.247
258
SCR001 Secretory Meningioma 40 0.247
259
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.247
260
WHP002 Whiplash 35 0.247
261
P PSR002 Psoriasis 63 0.247
262
HYP047 Hypertropia 23 0.247
263
P DBT009 Diabetes Mellitus 67 0.247
264
c ACT075 Acute Myocardial Infarction 55 0.247
265
P PLM064 Pulmonary Sequestration 22 0.247
266
MLT116 Multiple System Atrophy, Parkinsonian Type 29 0.247
267
THY029 Thyroid Carcinoma 54 0.247
268
P MPL001 Maple Syrup Urine Disease 69 0.221
269
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 0.221
270
ISL122 Isolated Growth Hormone Deficiency, Type Iii, with Agammaglobulinemia 36 0.221
271
RHB024 Rhabdomyosarcoma 2 65 0.221
272
c MCR115 Microvascular Complications of Diabetes 5 65 0.221
273
MNT308 Mental Retardation with Optic Atrophy, Deafness, and Seizures 27 0.221
274
c MCR112 Microvascular Complications of Diabetes 2 42 0.221
275
c JVN061 Juvenile Arthritis 56 0.221
276
P INF037 Inflammatory Bowel Disease 53 0.221
277
MLD018 Mild Cognitive Impairment 48 0.221
278
CMB007 Combined Immunodeficiency 56 0.221
279
c PRC016 Pre-Eclampsia 64 0.221
280
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.221
281
ISL003 Isolated Growth Hormone Deficiency 57 0.221
282
RTH007 Rothmund-Thomson Syndrome, Type 1 37 0.221
283
P MCR129 Microvascular Complications of Diabetes 1 68 0.221
284
END057 Endometrial Cancer 71 0.221
285
HRN029 Hearing Loss, Noise-Induced 37 0.221
286
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 58 0.221
287
HMP005 Hemiplegia 53 0.221
288
P PRS038 Personality Disorder 65 0.221
289
PHY002 Physical Disorder 41 0.221
290
P URN019 Urinary Tract Infection 49 0.221
291
P PTS002 Ptosis 52 0.221
292
SPN369 Spinal Disease 43 0.221
293
c HRD202 Hereditary Lymphedema I 55 0.221
294
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.221
295
c ACT073 Acute Leukemia 59 0.221
296
P CND004 Candidiasis 57 0.221
297
P END044 Endometriosis 62 0.221
298
ADN018 Adenoma 58 0.221
299
PRP016 Paraplegia 52 0.221
300
FBR047 Fibromyalgia 58 0.221
301
SHL001 Shoulder Impingement Syndrome 35 0.221
302
BLR002 Bile Reflux 38 0.221
303
XNT001 Xanthogranulomatous Pyelonephritis 30 0.221
304
P HRT032 Heart Disease 84 0.221
305
INT002 Intermittent Claudication 61 0.221
306
P URT039 Urticaria 57 0.221
307
PSY004 Psychotic Disorder 66 0.221
308
ISL125 Isolated Growth Hormone Deficiency Type Iii 39 0.221
309
GLM045 Glioma 62 0.221
310
SVR060 Severe X-Linked Intellectual Disability, Gustavson Type 24 0.221
311
SPS057 Spasticity 43 0.221
312
P PRD008 Periodontitis 64 0.221
313
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 33 0.221
314
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.221
315
ETN001 Eating Disorder 59 0.221
316
NPH018 Nephrogenic Systemic Fibrosis 49 0.221
317
TRG022 Triglyceride Deposit Cardiomyovasculopathy 19 0.221
318
PRS129 Prostatic Hyperplasia, Benign 48 0.191
319
P ATX030 Ataxia-Telangiectasia 80 0.191
320
c MCR133 Microvascular Complications of Diabetes 4 41 0.191
321
WST005 West Nile Virus 55 0.191
322
TND004 Tendinopathy 45 0.191
323
TND005 Tendinitis 54 0.191
324
ADN011 Adenoid Cystic Carcinoma 68 0.191
325
c MGR028 Migraine with or Without Aura 1 64 0.191
326
OBS002 Obsessive-Compulsive Disorder 68 0.191
327
P MYC084 Mycobacterium Tuberculosis 1 68 0.191
328
c MCR113 Microvascular Complications of Diabetes 3 52 0.191
329
c MCR130 Microvascular Complications of Diabetes 6 41 0.191
330
c MCR120 Microvascular Complications of Diabetes 7 47 0.191
331
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.191
332
ALP100 Alpha-Thalassemia/mental Retardation Syndrome, X-Linked 61 0.191
333
P RSP003 Respiratory Failure 74 0.191
334
P TMP003 Temporal Arteritis 68 0.191
335
P PLY019 Polyneuropathy 53 0.191
336
PRS021 Prostatic Adenoma 43 0.191
337
P CYS039 Cystic Kidney Disease 52 0.191
338
P INF032 Infertility 60 0.191
339
RCT015 Reactive Arthritis 60 0.191
340
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 56 0.191
341
P DMY001 Demyelinating Polyneuropathy 41 0.191
342
P DYS154 Dystonia 64 0.191
343
PRS045 Prostatic Hypertrophy 52 0.191
344
ANK001 Ankylosis 51 0.191
345
IMP005 Impotence 52 0.191
346
P VSC007 Vascular Disease 62 0.191
347
ACR007 Acromegaly 70 0.191
348
ENT001 Enterocele 42 0.191
349
NRG001 Neurogenic Bowel 30 0.191
350
TLN003 Telangiectasis 51 0.191
351
EPC002 Epicondylitis 43 0.191
352
TXC005 Toxic Shock Syndrome 62 0.191
353
P MLN007 Male Infertility 56 0.191
354
NRG002 Neurogenic Bladder 55 0.191
355
SKN016 Skin Disease 62 0.191
356
P BNG032 Benign Mesothelioma 53 0.191
357
BRS051 Breast Disease 58 0.191
358
PLG002 Plague 58 0.191
359
ANV001 Anovulation 46 0.191
360
P SPR120 Supranuclear Palsy, Progressive, 1 69 0.191
361
c ALP101 Alpha-Thalassemia 62 0.191
362
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.191
363
c RTN047 Retinitis Pigmentosa 18 45 0.191
364
SFT003 Soft Tissue Sarcoma 57 0.191
365
P THL005 Thalassemia 56 0.191
367
DYS073 Dysphagia 53 0.191
368
CRV002 Cervix Uteri Carcinoma in Situ 48 0.191
369
P BRN022 Bronchiectasis 59 0.191
370
SPN013 Spinal Canal Intradural Extramedullary Neoplasm 22 0.191
371
NM001 Noma 37 0.191
372
CRV045 Cervical Intraepithelial Neoplasia 38 0.191
373
ALL014 Allergic Encephalomyelitis 34 0.191
374
P ADT009 Auditory Neuropathy Spectrum Disorder 33 0.191
375
PRT036 Peritonitis 65 0.191
376
CHR066 Chronic Fatigue Syndrome 60 0.191
377
MLG079 Malignant Pleural Mesothelioma 42 0.191
378
DBT010 Diabetic Neuropathy 54 0.191
379
IRR002 Irritable Bowel Syndrome 65 0.191
380
GRW007 Growth Hormone Deficiency 47 0.191
381
HMP009 Haemophilus Influenzae 41 0.191
382
ORL011 Oral Cancer 60 0.191
383
P TYR004 Tyrosinemia 49 0.191
384
PRD026 Pre-Descemet Corneal Dystrophy 20 0.191
385
P OVR096 Overlap Myositis 27 0.191
386
CRV035 Cervical Cancer 72 0.156
387
P GST053 Gastric Cancer 82 0.156
388
NNK001 Nonaka Myopathy 58 0.156
389
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.156
390
ATS010 Autosomal Recessive Disease 42 0.156
391
DFF005 Diffuse Large B-Cell Lymphoma 55 0.156
392
SCR035 Sacral Agenesis with Vertebral Anomalies 39 0.156
393
c PCH010 Pachyonychia Congenita 3 43 0.156
394
OST003 Osteonecrosis 61 0.156
395
PNM005 Pneumonic Plague 47 0.156
396
P VNS003 Venous Insufficiency 54 0.156
397
RNL025 Renal Hypoplasia 46 0.156
398
P PLY014 Polycystic Kidney Disease 71 0.156
399
P MDL005 Medulloblastoma 75 0.156
400
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 57 0.156
401
c GLY008 Glycogen Storage Disease Ii 72 0.156
402
ENT011 Enterocolitis 55 0.156
403
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 0.156
404
CHR431 Chronic Venous Insufficiency 48 0.156
405
ADR041 Adrenal Cortical Adenoma 48 0.156
406
FML037 Female Breast Cancer 51 0.156
407
ING001 Inguinal Hernia 59 0.156
408
CRH005 Crohn's Colitis 53 0.156
409
P GLL020 Gallbladder Disease 57 0.156
410
HMN044 Human Immunodeficiency Virus Type 1 76 0.156
411
ALL003 Allergic Rhinitis 66 0.156
412
c MSC036 Muscular Dystrophy-Dystroglycanopathy , Type C, 5 64 0.156
413
c HYP836 Hypercholesterolemia, Familial, 1 73 0.156
414
INC002 Inclusion Body Myositis 57 0.156
415
c CND033 Candidiasis, Familial, 1 27 0.156
416
BRD004 Borderline Personality Disorder 53 0.156
417
P LKM071 Leukemia, Chronic Lymphocytic 74 0.156
418
LWC001 Low Compliance Bladder 44 0.156
419
LMY002 Leiomyoma 51 0.156
420
c SVR005 Severe Pre-Eclampsia 50 0.156
421
ISC004 Ischemia 61 0.156
422
CNG034 Congestive Heart Failure 69 0.156
423
P ACN011 Acne 55 0.156
424
ESN003 Eosinophilic Variant of Chromophobe Renal Cell Carcinoma 17 0.156
425
EXT007 Extracutaneous Mastocytoma 38 0.156
426
DNT012 Dental Caries 53 0.156
427
NNT012 Neonatal Jaundice 53 0.156
428
HYP016 Hypochondriasis 47 0.156
429
P HYP086 Hypothyroidism 69 0.156
430
CHL028 Childhood Type Dermatomyositis 58 0.156
431
SLC006 Silicosis 55 0.156
432
END011 Endometriosis of Ovary 40 0.156
433
P ADL010 Adult Respiratory Distress Syndrome 71 0.156
434
INT066 Interstitial Lung Disease 60 0.156
435
GNG013 Gingivitis 59 0.156
436
LNG039 Lung Squamous Cell Carcinoma 57 0.156
437
NRC003 Narcissistic Personality Disorder 25 0.156
438
P RHN004 Rhinitis 57 0.156
439
MST004 Mast Cell Neoplasm 41 0.156
440
P RTT002 Rett Syndrome 79 0.156
441
P SYS005 Systemic Scleroderma 73 0.156
442
P GST044 Gastritis 55 0.156
443
SMT007 Smith-Fineman-Myers Syndrome 32 0.156
444
P VSC011 Vasculitis 61 0.156
445
P INS002 in Situ Carcinoma 53 0.156
446
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.156
447
DYS030 Dysferlinopathy 38 0.156
448
P MTR014 Motor Neuron Disease 65 0.156
449
PLC007 Placental Abruption 47 0.156
450
ANC002 Anca-Associated Vasculitis 44 0.156
451
PPT005 Peptic Ulcer Disease 58 0.156
452
PRN019 Perinatal Necrotizing Enterocolitis 60 0.156
453
NCR015 Necrotizing Autoimmune Myopathy 31 0.156
454
QLT008 Qualitative or Quantitative Defects of Dysferlin 30 0.156
455
JVN060 Juvenile Idiopathic Inflammatory Myopathy 15 0.156
456
ART140 Arteries, Anomalies of 52 0.110
457
P MCH002 Machado-Joseph Disease 63 0.110
458
c PRD040 Periodontitis, Chronic 52 0.110
459
BRT005 Barth Syndrome 55 0.110
460
c TYR012 Tyrosinemia, Type I 61 0.110
461
LPD012 Lipoid Congenital Adrenal Hyperplasia 68 0.110
462
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.110
463
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.110
464
HMC014 Homocysteinemia 52 0.110
465
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.110
466
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.110
467
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.110
468
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 41 0.110
469
P DNG005 Dengue Virus 55 0.110
470
LPP008 Lipoprotein Quantitative Trait Locus 65 0.110
471
ANG054 Angina Pectoris 65 0.110
472
SZR028 Seizures, Scoliosis, and Macrocephaly/microcephaly Syndrome 36 0.110
473
P ASP001 Asperger Syndrome 48 0.110
474
HYP020 Hyperprolactinemia 63 0.110
475
PRP036 Peripheral T-Cell Lymphoma 52 0.110
476
LWG006 Low Grade Glioma 41 0.110
477
BNR002 Bone Resorption Disease 47 0.110
478
MCS002 Mucositis 55 0.110
479
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.110
480
NNL006 Non-Alcoholic Steatohepatitis 54 0.110
481
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.110
482
OTT002 Otitis Media 71 0.110
483
ALC007 Alcohol Dependence 65 0.110
484
c ART115 Aortic Valve Disease 1 72 0.110
485
BRK010 Burkitt Lymphoma 66 0.110
486
P LNG032 Lung Cancer 98 0.110
487
CRB011 Cerebrotendinous Xanthomatosis 65 0.110
488
DFN256 Deafness and Myopia 32 0.110
489
P SLP006 Sleep Apnea 69 0.110
490
SXL003 Sexual Disorder 49 0.110
491
MTB004 Metabolic Acidosis 48 0.110
492
c CNG006 Congenital Hypothyroidism 63 0.110
493
CLR108 Colorectal Adenoma 63 0.110
494
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.110
495
XNT003 Xanthomatosis 48 0.110
496
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.110
497
P DRM053 Dermatitis, Atopic 65 0.110
498
SCK003 Sickle Cell Anemia 74 0.110
499
P MYC007 Myocardial Infarction 69 0.110
500
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.110
501
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.110
502
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.110
503
P HYP750 Hypertriglyceridemia, Familial 62 0.110
504
CNT106 Centralopathic Epilepsy 34 0.110
505
MTN003 Motion Sickness 50 0.110
506
c TBL031 Tubulointerstitial Kidney Disease, Autosomal Dominant, 1 48 0.110
507
CRD132 Cardiac Conduction Defect 59 0.110
508
CRT072 Creutzfeldt-Jakob Disease 67 0.110
509
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.110
510
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.110
511
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.110
512
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.110
513
P FRG001 Fragile X Syndrome 70 0.110
514
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.110
515
FBR012 Fabry Disease 71 0.110
516
CHL122 Cholesteatoma of Middle Ear 51 0.110
517
HRW001 Hair Whorl 35 0.110
518
TBC004 Tobacco Addiction 63 0.110
519
c TBR025 Tuberous Sclerosis 1 84 0.110
520
URT049 Urate Oxidase, Pseudogene 24 0.110
521
c WLM013 Wilms Tumor 1 65 0.110
522
P ALC033 Alcohol Use Disorder 67 0.110
523
HYP060 Hyperinsulinism 53 0.110
524
MSC190 Muscular Disease 36 0.110
525
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.110
526
HYP457 Hypertrophic Scars 42 0.110
527
CHR100 Chronic Ulcer of Skin 57 0.110
528
HYP030 Hypoactive Sexual Desire Disorder 39 0.110
529
MST005 Mastitis 52 0.110
530
BLR001 Biliary Atresia 55 0.110
531
P TBR001 Tuberous Sclerosis 69 0.110
532
ACT078 Acute Porphyria 50 0.110
533
P ANT006 Antiphospholipid Syndrome 55 0.110
534
CRV040 Cervix Carcinoma 50 0.110
535
P INT068 Intestinal Disease 53 0.110
536
P ART018 Aortic Valve Insufficiency 52 0.110
537
P PRP019 Peripheral Nervous System Disease 57 0.110
538
KRT002 Keratomalacia 54 0.110
539
PLC006 Placental Choriocarcinoma 38 0.110
540
NRN004 Neuroendocrine Tumor 55 0.110
541
OPT003 Opiate Dependence 49 0.110
542
P GLL022 Guillain-Barre Syndrome 59 0.110
543
P PRP029 Porphyria 60 0.110
544
P CRD246 Cardiovascular System Disease 55 0.110
545
AMN001 Amenorrhea 53 0.110
546
FCL012 Facial Paralysis 49 0.110
547
THY122 Thyroid Gland Cancer 59 0.110
548
NDL007 Nodular Goiter 48 0.110
549
HMS001 Hemosiderosis 48 0.110
550
GTR002 Goiter 52 0.110
551
P OTS001 Otosclerosis 49 0.110
552
FML035 Familial Hyperlipidemia 55 0.110
553
P LVR013 Liver Disease 68 0.110
554
TST014 Testicular Cancer 51 0.110
555
BRN005 Brain Glioblastoma Multiforme 34 0.110
556
P OLG002 Oligodendroglioma 66 0.110
557
CHR074 Choriocarcinoma 46 0.110
558
THR016 Thrombophlebitis 50 0.110
559
HMT002 Hematologic Cancer 61 0.110
560
PNC034 Pancreas Disease 49 0.110
561
BNG009 Benign Epilepsy with Centrotemporal Spikes 60 0.110
562
P LPS002 Liposarcoma 64 0.110
563
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.110
564
c LKM061 Leukemia, Acute Myeloid 83 0.110
565
P CTR177 Citrullinemia, Type Ii, Adult-Onset 55 0.110
566
c PNC106 Pancreatic Agenesis 1 51 0.110
567
c RNG016 Ring Chromosome 20 26 0.110
568
DRM006 Dermatitis 62 0.110
569
GST045 Gastroenteritis 58 0.110
570
OPD006 Opioid Addiction 48 0.110
571
c RNG022 Ring Chromosome 6 28 0.110
572
RHH001 Rohhad 27 0.110
573
IDP085 Idiopathic Infantile Hypercalcemia 32 0.110
574
P HYP265 Hypotonia 42 0.110
575
SBS004 Substance Dependence 46 0.110
576
INT075 Intracranial Hypertension 52 0.110
577
LNG030 Lung Adenoma 37 0.110
578
YLL002 Yellow Fever 61 0.110
579
PTH003 Pathologic Nystagmus 52 0.110
580
P KDN018 Kidney Disease 72 0.110
581
P PNM007 Pneumonia 64 0.110
582
P HDC001 Headache 56 0.110
583
c RNG008 Ring Chromosome 13 30 0.110
584
TRM010 Traumatic Brain Injury 50 0.110
585
PNC019 Pancreatoblastoma 39 0.110
586
HPT022 Hepatoblastoma 54 0.110
587
CCN001 Cocaine Dependence 48 0.110
588
P HYP121 Hypoalphalipoproteinemia 42 0.110
589
PLM033 Pulmonary Embolism 58 0.110
590
DSS012 Disseminated Infection with Mycobacterium Avium Complex 18 0.110
591
EXR007 Exercise-Induced Anaphylaxis 23 0.110
592
MYC019 Mycobacterium Marinum 29 0.110
593
LYM019 Lymphosarcoma 46 0.110
594
ACD003 Acid Sphingomyelinase Deficiency 30 0.110
595
P ATR005 Atrophic Gastritis 50 0.110
596
PST092 Posttransplant Acute Limbic Encephalitis 29 0.110
597
P RNG032 Ring Chromosome 39 0.110
598
DSR031 Disorder of Copper Metabolism 25 0.110
599
P RRH023 Rare Hereditary Hemochromatosis 53 0.110
600
RPD006 Rapid-Onset Childhood Obesity-Hypothalamic Dysfunction-Hypoventilation-Autonomic Dysregulation Syndrome 28 0.110
601
CLC053 Colchicine Poisoning 23 0.110
602
ARG004 Argyria 26 0.110
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