Search results for Succinic acid

834 hits were found for Succinic acid

# Family MCID Name MIFTS Score
1
ARG002 Argininosuccinic Aciduria 60 3.441
2
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.315
3
P LVR013 Liver Disease 68 0.293
4
CHL068 Cholestasis 60 0.277
5
P NRB001 Neuroblastoma 71 0.274
6
DPR016 Depression 63 0.265
7
FTT001 Fatty Liver Disease 61 0.263
8
48X005 48,xyyy 39 0.263
9
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 58 0.256
10
P CLR023 Colorectal Cancer 98 0.254
11
MNT002 Mental Depression 57 0.251
12
P KDN018 Kidney Disease 70 0.250
13
P SZR006 Seizure Disorder 58 0.250
14
ISC004 Ischemia 60 0.246
15
P BRS047 Breast Cancer 96 0.243
16
LVR012 Liver Cirrhosis 63 0.243
17
NRL016 Neural Tube Defects 82 0.241
18
VSL002 Visual Epilepsy 58 0.241
19
c HYP595 Hypertension, Essential 84 0.240
20
P DRR001 Diarrhea 57 0.231
21
P PRG013 Paraganglioma 52 0.230
22
MTB004 Metabolic Acidosis 50 0.229
23
P PHC003 Pheochromocytoma 71 0.229
24
P MJR001 Major Depressive Disorder 68 0.229
25
ACT119 Acute Promyelocytic Leukemia 63 0.227
26
HYP266 Hypoxia 56 0.224
27
HLX001 Helix Syndrome 47 0.222
28
ADR040 Adrenal Gland Pheochromocytoma 46 0.221
29
P PRS040 Prostate Cancer 97 0.220
30
c MGR028 Migraine with or Without Aura 1 69 0.219
31
LWC001 Low Compliance Bladder 42 0.218
32
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.217
33
HYP014 Hyperuricemia 51 0.216
34
P HRT032 Heart Disease 75 0.214
35
CLT003 Colitis 62 0.213
36
HYP066 Hyperglycemia 61 0.209
37
P ENC018 Encephalopathy 61 0.207
38
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.207
39
P LKM002 Leukemia 66 0.206
40
HYP056 Hypoglycemia 66 0.204
41
P DDN001 Duodenal Ulcer 50 0.204
42
ALL026 Allergic Hypersensitivity Disease 64 0.203
43
LPD008 Lipid Metabolism Disorder 62 0.200
44
CNG034 Congestive Heart Failure 70 0.200
45
P HPT023 Hepatocellular Carcinoma 100 0.199
46
P GLM045 Glioma 63 0.197
47
ULC004 Ulcerative Colitis 73 0.197
48
GLL048 Glial Tumor 45 0.195
49
OST012 Osteoarthritis 78 0.194
50
ADL002 Adult Syndrome 69 0.194
51
ADN018 Adenoma 58 0.193
52
DRM006 Dermatitis 61 0.190
53
P CRN300 Coronary Heart Disease 1 63 0.189
54
DFC004 Deficiency Anemia 75 0.189
55
P MYP004 Myopathy 64 0.189
56
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.188
57
BNR002 Bone Resorption Disease 48 0.187
58
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.187
59
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.186
60
GLB015 Glioblastoma Multiforme 75 0.185
61
IRN002 Iron Metabolism Disease 57 0.185
62
CRB039 Cerebrovascular Disease 69 0.181
63
END040 Endogenous Depression 54 0.181
64
PPT005 Peptic Ulcer Disease 58 0.181
65
GT001 Gout 63 0.179
66
ATM095 Autoimmune Disease 61 0.179
67
NRT001 Neurotic Disorder 52 0.178
68
STT001 Status Epilepticus 59 0.178
69
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.177
70
P VSC007 Vascular Disease 63 0.177
71
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.176
72
P INF037 Inflammatory Bowel Disease 56 0.173
73
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.172
74
OCL069 Ocular Motor Apraxia 51 0.172
75
PRT037 Pertussis 65 0.172
76
P OVR042 Ovarian Cancer 89 0.172
77
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.171
78
SPN186 Spinal Cord Injury 60 0.171
79
c RHB024 Rhabdomyosarcoma 2 65 0.171
80
P MYC007 Myocardial Infarction 70 0.171
81
STR067 Stroke, Ischemic 80 0.171
82
ATH013 Atherosclerosis Susceptibility 66 0.171
83
P HNT016 Huntington Disease 71 0.170
84
P ALZ034 Alzheimer Disease 88 0.170
85
P ADN016 Adenocarcinoma 64 0.170
86
P PSR002 Psoriasis 62 0.169
87
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.169
88
P GST053 Gastric Cancer 83 0.168
89
P LYM031 Lymphocytic Leukemia 55 0.168
90
P HYP750 Hypertriglyceridemia, Familial 61 0.168
91
PST011 Pustulosis of Palm and Sole 52 0.168
92
P CRN018 Coronary Artery Anomaly 63 0.167
93
c CHR684 Chronic Kidney Disease 66 0.167
94
P HYP265 Hypotonia 42 0.166
95
PLM001 Pulmonary Tuberculosis 70 0.165
96
47X002 47,xyy 49 0.164
97
c GLL024 Gallbladder Disease 1 52 0.162
98
P DBT009 Diabetes Mellitus 64 0.161
99
PRS045 Prostatic Hypertrophy 52 0.161
100
c ACT068 Acute Cystitis 63 0.161
101
P TRN020 Turner Syndrome 65 0.160
102
c PCH010 Pachyonychia Congenita 3 43 0.159
103
P LNG032 Lung Cancer 97 0.158
104
NNL006 Non-Alcoholic Steatohepatitis 51 0.157
105
CNS004 Constipation 57 0.156
106
P NRP001 Neuropathy 56 0.155
107
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.155
108
P MYL006 Myeloid Leukemia 60 0.154
109
P PNC035 Pancreatic Cancer 84 0.153
110
CYS001 Cystic Fibrosis 80 0.153
111
P HDC001 Headache 57 0.153
112
P CRD246 Cardiovascular System Disease 56 0.152
113
NTR005 Nutritional Deficiency Disease 61 0.152
114
P LCT001 Lactic Acidosis 51 0.152
115
PRS021 Prostatic Adenoma 51 0.151
116
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.150
117
ART140 Arteries, Anomalies of 53 0.150
118
c LKM061 Leukemia, Acute Myeloid 83 0.150
119
DWN001 Down Syndrome 70 0.149
120
HRW001 Hair Whorl 36 0.149
121
PRS129 Prostatic Hyperplasia, Benign 49 0.149
122
P BLD134 Bladder Cancer 78 0.147
123
OST159 Osteogenic Sarcoma 66 0.147
124
c VSC019 Vesicoureteral Reflux 1 59 0.146
125
HYP060 Hyperinsulinism 54 0.146
126
P EPL164 Epilepsy 71 0.145
127
HYP781 Hypoascorbemia 50 0.145
128
CHL079 Children's Interstitial Lung Disease 27 0.144
129
c DNT047 Dentinogenesis Imperfecta Type 2 33 0.144
130
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.143
131
BRN071 Brain Injury 49 0.142
132
CYT002 Cytokine Deficiency 44 0.142
133
P MLT020 Multiple Sclerosis 72 0.141
134
P LYM118 Lymphoma 68 0.141
135
GST019 Gastrointestinal Stromal Tumor 76 0.140
136
URT049 Urate Oxidase, Pseudogene 25 0.139
137
END030 End Stage Renal Failure 58 0.139
138
GST023 Gastric Ulcer 53 0.139
139
ATS010 Autosomal Recessive Disease 48 0.138
140
P BPL003 Bipolar Disorder 56 0.137
141
CRV035 Cervical Cancer 76 0.137
142
c ACT075 Acute Myocardial Infarction 56 0.137
143
c INH020 Inherited Metabolic Disorder 46 0.137
144
c ACT071 Acute Kidney Failure 59 0.136
145
c MJR024 Major Affective Disorder 9 41 0.136
146
c MJR022 Major Affective Disorder 8 38 0.136
147
ANX004 Anoxia 42 0.136
148
DBT010 Diabetic Neuropathy 55 0.136
149
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.135
150
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.135
151
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.135
152
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.135
153
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.135
154
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.135
155
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.135
156
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.135
157
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.135
158
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.135
159
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.135
160
P HYP086 Hypothyroidism 68 0.135
161
P NTR004 Neutropenia 63 0.135
162
SKN016 Skin Disease 63 0.135
163
P ATS364 Autism 65 0.134
164
AGN016 Aging 56 0.134
165
P CNR004 Cone-Rod Dystrophy 2 71 0.134
166
TRM010 Traumatic Brain Injury 53 0.134
167
THY029 Thyroid Carcinoma 59 0.133
168
SQM006 Squamous Cell Carcinoma 60 0.132
169
LNG099 Lung Disease 61 0.132
170
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.132
171
TXC005 Toxic Shock Syndrome 61 0.132
172
ATX019 Ataxia with Vitamin E Deficiency 48 0.130
173
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.129
174
MYL069 Myeloma, Multiple 85 0.129
175
P SCH015 Schizophrenia 75 0.129
176
PHN003 Phenylketonuria 75 0.129
177
c MCR120 Microvascular Complications of Diabetes 7 47 0.128
178
c MCR113 Microvascular Complications of Diabetes 3 52 0.128
179
c MCR130 Microvascular Complications of Diabetes 6 41 0.127
180
c MCR133 Microvascular Complications of Diabetes 4 41 0.127
181
ALC007 Alcohol Dependence 66 0.127
182
URM002 Uremia 49 0.127
183
P RHM011 Rheumatoid Arthritis 80 0.126
184
CRH001 Crohn's Disease 74 0.126
185
P LKM062 Leukemia, Acute Lymphoblastic 68 0.125
186
c ATR087 Atrial Standstill 1 74 0.124
187
RCK004 Rickets 69 0.123
188
P CTR002 Cataract 60 0.123
189
P PRD008 Periodontitis 62 0.123
190
P PYL005 Pyelonephritis 56 0.123
191
VTM002 Vitamin B12 Deficiency 48 0.123
192
P ART022 Arthritis 70 0.122
193
c ATS007 Autism Spectrum Disorder 67 0.122
194
P GLM007 Glomerulonephritis 57 0.121
195
PRT036 Peritonitis 65 0.121
196
P KDN017 Kidney Cancer 61 0.120
197
P PRP019 Peripheral Nervous System Disease 57 0.119
198
HMP009 Haemophilus Influenzae 42 0.119
199
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.119
200
P MSC005 Muscular Dystrophy 66 0.119
201
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.118
202
ESP021 Esophageal Cancer 90 0.118
203
P ATR011 Atrial Fibrillation 66 0.118
204
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.118
205
LYM019 Lymphosarcoma 47 0.117
206
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.117
207
BRR014 Barrett Esophagus 64 0.117
208
CHL123 Chlamydia 59 0.116
209
CRB004 Cerebral Artery Occlusion 44 0.116
210
P BNG032 Benign Mesothelioma 45 0.116
211
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.116
212
TTN003 Tetanus 64 0.116
213
P BRS044 Breast Adenocarcinoma 59 0.116
214
P RTN024 Retinoblastoma 72 0.116
215
P RHN004 Rhinitis 57 0.116
216
c FML008 Familial Retinoblastoma 53 0.115
217
P PNM007 Pneumonia 68 0.115
218
OST003 Osteonecrosis 61 0.115
219
c FNC043 Fanconi Anemia, Complementation Group E 62 0.115
220
c ACT073 Acute Leukemia 58 0.114
221
ANG054 Angina Pectoris 66 0.114
222
P RSP003 Respiratory Failure 74 0.114
223
ANX010 Anxiety 72 0.114
224
PLM010 Pulmonary Edema 55 0.114
225
BRN024 Bronchitis 68 0.113
226
BCT022 Bacterial Infectious Disease 56 0.113
227
P PRK057 Parkinson Disease, Late-Onset 76 0.113
228
P DMN002 Dementia 67 0.113
229
P ALP008 Alopecia 56 0.112
230
RHM027 Rheumatic Disease 56 0.112
231
IRN001 Iron Deficiency Anemia 58 0.111
232
c PRS136 Prostate Cancer, Hereditary, 6 33 0.111
233
c PRS130 Prostate Cancer, Hereditary, 8 32 0.111
234
THR024 Thrombosis 56 0.111
235
PLM033 Pulmonary Embolism 59 0.111
236
ALL014 Allergic Encephalomyelitis 39 0.110
237
P MCR115 Microvascular Complications of Diabetes 5 66 0.110
238
P NSP012 Nasopharyngeal Carcinoma 67 0.110
239
SCH014 Schistosomiasis 56 0.109
240
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.109
241
P HYP076 Hyperthyroidism 55 0.108
242
P LPS004 Lupus Erythematosus 61 0.108
243
P FBR017 Fibrosarcoma 56 0.108
244
c ACT027 Acute Pancreatitis 59 0.108
245
SVR004 Severe Combined Immunodeficiency 73 0.108
246
c SYS001 Systemic Lupus Erythematosus 86 0.107
247
CLN015 Colon Adenocarcinoma 63 0.107
248
P PNC044 Pancreatitis 61 0.107
249
DNT012 Dental Caries 51 0.107
250
c THR092 Thrombophilia Due to Thrombin Defect 73 0.106
251
VCC001 Vaccinia 49 0.106
252
MTH071 Methane Production 26 0.106
253
CRD132 Cardiac Conduction Defect 59 0.105
254
SPP010 Suppressor of Tumorigenicity 3 51 0.105
255
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.105
256
P THR014 Thrombocytopenia 68 0.104
257
P OVR082 Overgrowth Syndrome 50 0.104
258
P SKN015 Skin Carcinoma 67 0.104
259
P TRM003 Tremor 53 0.104
260
P ART021 Arteriosclerosis 54 0.104
261
AST005 Asthma 77 0.104
262
P EXN002 Exanthem 57 0.104
263
MLN008 Melanoma 69 0.103
264
P MNN013 Meningitis 65 0.102
265
P DYS154 Dystonia 65 0.102
266
c VRL010 Viral Hepatitis 51 0.102
267
IMM167 Immune Deficiency Disease 78 0.102
268
P PRP029 Porphyria 62 0.102
269
PNG002 Pain Agnosia 51 0.102
270
c SML038 Small Cell Cancer of the Lung 65 0.101
271
P INF032 Infertility 57 0.101
272
SBC016 Subacute Delirium 44 0.101
273
P GLM040 Glioma Susceptibility 1 81 0.101
274
P CRD119 Cardiac Arrest 67 0.100
275
ALL003 Allergic Rhinitis 67 0.100
276
URN010 Urinary Tract Obstruction 57 0.100
277
P AST007 Astrocytoma 50 0.099
278
MSC007 Muscle Hypertrophy 63 0.099
279
MDD011 Mood Disorder 62 0.099
280
CLF027 Cleft Palate, Isolated 64 0.099
281
BRN004 Brain Edema 55 0.098
283
P MTC133 Mitochondrial Myopathy 49 0.098
284
CHL004 Cholelithiasis 49 0.097
285
PSY004 Psychotic Disorder 67 0.097
286
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.096
287
P CYS018 Cystitis 59 0.096
288
GLS018 Glass Syndrome 53 0.096
289
c DLT002 Dilated Cardiomyopathy 79 0.095
290
c PNS012 Paine Syndrome 61 0.095
291
CNT047 Contact Dermatitis 57 0.095
292
PRG017 Paraganglioma and Gastric Stromal Sarcoma 52 0.095
293
P MTH008 Methylmalonic Acidemia 51 0.094
294
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.094
295
BRN028 Brain Cancer 73 0.093
296
PRP027 Peripheral Vascular Disease 71 0.093
297
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.093
298
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.093
299
P MYC008 Myocarditis 59 0.092
300
DPH001 Diphtheria 60 0.092
301
RNL077 Renal Fibrosis 47 0.092
302
P URT039 Urticaria 58 0.092
303
EYD002 Eye Disease 58 0.092
304
MLR004 Malaria 80 0.091
305
HMS001 Hemosiderosis 54 0.091
306
c MST023 Mesothelioma, Malignant 57 0.091
307
P MTC069 Mitochondrial Disorders 56 0.091
308
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.091
309
c BRN108 Branchiootic Syndrome 1 61 0.091
310
c LKM071 Leukemia, Chronic Lymphocytic 79 0.091
311
P PLM037 Pulmonary Hypertension 68 0.091
312
P MLN007 Male Infertility 56 0.091
313
CMM005 Common Cold 56 0.090
314
P PTT006 Pituitary Adenoma 54 0.090
315
P MYC033 Myoclonus 46 0.090
316
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.090
317
P RRH023 Rare Hereditary Hemochromatosis 41 0.090
318
MTC020 Mitochondrial Complex Ii Deficiency 54 0.089
319
PRN011 Pernicious Anemia 52 0.089
320
P LNG064 Lung Cancer Susceptibility 3 77 0.088
321
NRF026 Neurofibromatosis, Type Iv, of Riccardi 63 0.088
322
LYM040 Lymphoblastic Lymphoma 54 0.088
323
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.088
324
GST050 Gastrointestinal System Disease 56 0.088
325
P ADL010 Adult Respiratory Distress Syndrome 63 0.088
326
P GRF003 Graft-Versus-Host Disease 71 0.088
327
ORL015 Oral Squamous Cell Carcinoma 43 0.087
328
GST045 Gastroenteritis 59 0.087
329
P HYP061 Hypertrophic Cardiomyopathy 66 0.087
330
c MCR129 Microvascular Complications of Diabetes 1 66 0.087
331
ENT004 Enthesopathy 48 0.087
332
BLD044 Bladder Disease 48 0.087
333
P MYC084 Mycobacterium Tuberculosis 1 68 0.087
334
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.086
335
NWC001 Newcastle Disease 44 0.086
336
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.085
337
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.085
338
HYD002 Hydronephrosis 59 0.085
339
P SLP005 Sleep Disorder 59 0.085
340
P HML002 Hemolytic Anemia 62 0.085
341
INT007 Intermediate Coronary Syndrome 55 0.084
342
CHL067 Cholecystitis 58 0.084
343
P CHR345 Chronic Pain 50 0.084
344
c MTC059 Mitochondrial Dna Depletion Syndrome 5 43 0.084
345
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.084
346
ENT011 Enterocolitis 50 0.084
347
P SBR004 Seborrheic Dermatitis 45 0.083
348
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 35 0.083
349
TRN015 Transient Cerebral Ischemia 62 0.083
350
HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 56 0.083
351
P INS002 in Situ Carcinoma 52 0.083
352
P HYP098 Hypereosinophilic Syndrome 66 0.083
353
P NPH012 Nephrotic Syndrome 63 0.083
354
MST005 Mastitis 53 0.083
355
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.082
356
LSH001 Leishmaniasis 63 0.082
357
P KLZ004 Kala-Azar 1 41 0.082
358
LYM133 Lymphoma, Hodgkin, Classic 69 0.082
359
GTR002 Goiter 52 0.082
360
P OBS001 Obstructive Jaundice 48 0.082
361
c CHR682 Chronic Bilirubin Encephalopathy 38 0.082
362
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.081
363
P URF003 Urofacial Syndrome 1 57 0.081
364
URN009 Urinary System Disease 48 0.081
365
P THL005 Thalassemia 60 0.081
366
TYP007 Typhoid Fever 63 0.080
367
END057 Endometrial Cancer 74 0.080
368
VSC002 Vascular Dementia 57 0.080
369
PRP030 Purpura 55 0.080
370
c HPT003 Hepatitis a 63 0.079
371
c BSL007 Basal Cell Carcinoma 68 0.079
372
c INF071 Inflammatory Bowel Disease 1 68 0.079
373
P PLY014 Polycystic Kidney Disease 59 0.079
374
P CND004 Candidiasis 57 0.078
375
c CHR064 Chronic Monocytic Leukemia 34 0.078
376
MSL001 Measles 61 0.078
377
ACY011 Acyl-Coa Dehydrogenase Deficiency 37 0.078
378
c PRD040 Periodontitis, Chronic 54 0.078
379
HDN002 Head Injury 45 0.078
380
P ALP009 Alopecia Areata 60 0.078
381
c ATS307 Autosomal Recessive Cerebellar Ataxia 41 0.078
382
BLR001 Biliary Atresia 50 0.078
383
ALL010 Allergic Contact Dermatitis 55 0.077
384
MMM001 Mammary Paget's Disease 53 0.077
385
P TCL004 T-Cell Leukemia 47 0.077
386
IGR001 Ige Responsiveness, Atopic 59 0.076
387
P RCT021 Rectum Cancer 53 0.076
388
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 57 0.076
389
ORG002 Organic Acidemia 43 0.076
390
PNC001 Pancytopenia 54 0.076
391
c ACT042 Acute Pyelonephritis 44 0.076
392
RHM001 Rheumatic Fever 61 0.076
393
c FML001 Familial Atrial Fibrillation 66 0.075
394
P SCK005 Sickle Cell Disease 50 0.075
395
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.075
396
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.074
397
FBR047 Fibromyalgia 59 0.074
398
RTN017 Retinal Detachment 60 0.074
399
PTT037 Pituitary Tumors 44 0.074
400
CHG001 Chagas Disease 66 0.074
401
SPN041 Spinal Cord Disease 56 0.074
402
PRP080 Peripheral Artery Disease 53 0.074
403
URT010 Ureteral Obstruction 46 0.074
404
P SHR001 Short Bowel Syndrome 52 0.073
405
KHL003 Kohlschutter-Tonz Syndrome 64 0.073
406
c PRG021 Paragangliomas 4 37 0.073
407
MLK006 Milk Allergy 48 0.072
408
AMN003 Amnestic Disorder 54 0.072
409
DBT002 Diabetic Autonomic Neuropathy 41 0.072
410
P NRV007 Nervous System Disease 66 0.072
411
DSS008 Disease of Mental Health 57 0.072
412
AMN006 Aminoaciduria 38 0.072
413
GNG013 Gingivitis 59 0.071
414
P THY032 Thyroiditis 53 0.071
415
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.071
416
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.071
417
P FRD001 Friedreich Ataxia 63 0.071
418
CYT018 Cytochrome P450 2d6 Variant 27 0.071
419
P HYD006 Hydrocephalus 65 0.070
420
MTC005 Mitochondrial Metabolism Disease 48 0.069
421
SCR011 Scrapie 38 0.069
422
LMY003 Leiomyomatosis 43 0.069
423
INT020 Intravenous Leiomyomatosis 36 0.069
424
c BCT007 Bacterial Meningitis 55 0.069
425
49X006 49, Xxxxy Syndrome 41 0.069
426
P MVM001 Movement Disease 61 0.068
427
ANR007 Anorexia Nervosa 63 0.068
428
ACT058 Active Peptic Ulcer Disease 55 0.068
429
BTN004 Biotin Deficiency 38 0.068
430
LGH007 Leigh Syndrome 70 0.068
431
PLC008 Placenta Disease 49 0.067
432
c SPN225 Spondyloarthropathy 1 73 0.067
433
BRK010 Burkitt Lymphoma 67 0.067
434
P RHB003 Rhabdomyosarcoma 62 0.067
435
P VSC011 Vasculitis 62 0.067
436
c HNT011 Huntington Disease-Like 3 38 0.067
437
P PRS038 Personality Disorder 65 0.066
438
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 50 0.066
439
NRG002 Neurogenic Bladder 54 0.066
440
c GRV008 Graves Disease 1 55 0.066
441
NRM022 Neurometabolic Disease 25 0.066
442
OST017 Osteomyelitis 64 0.065
443
BCT002 Bacterial Vaginosis 52 0.065
444
P MJR007 Major Affective Disorder 1 43 0.065
445
SCK003 Sickle Cell Anemia 72 0.065
446
P NRC002 Narcolepsy 51 0.065
447
PST021 Postpartum Depression 50 0.065
448
RTC012 Reticuloendotheliosis, X-Linked 40 0.064
449
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.064
450
OBS002 Obsessive-Compulsive Disorder 68 0.064
451
RST023 Resting Heart Rate, Variation in 41 0.064
452
AMN002 Amino Acid Metabolic Disorder 40 0.064
453
LYM027 Lymphopenia 57 0.064
454
PRP016 Paraplegia 53 0.064
455
ACT228 Acute Radiation Syndrome 29 0.064
456
P FNC004 Fanconi Syndrome 50 0.064
457
HPT014 Hepatorenal Syndrome 50 0.063
458
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 65 0.063
459
P OPN001 Open-Angle Glaucoma 49 0.063
460
HYP141 Hyperphenylalaninemia 38 0.063
461
NRN004 Neuroendocrine Tumor 55 0.062
462
P MYG005 Myoglobinuria 43 0.062
463
CRB037 Cerebral Palsy 68 0.062
464
CRC021 Carcinosarcoma 61 0.062
465
c MJR003 Major Affective Disorder 6 33 0.061
466
c MJR006 Major Affective Disorder 5 33 0.061
467
P STR092 Striatal Degeneration, Autosomal Dominant 2 43 0.061
468
P GRV001 Graves' Disease 55 0.061
469
P BRB001 Beriberi 44 0.061
470
NRM005 Neuromuscular Disease 63 0.061
471
c MJR008 Major Affective Disorder 2 34 0.060
473
c MJR023 Major Affective Disorder 7 33 0.060
474
c MJR004 Major Affective Disorder 4 28 0.060
475
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.060
476
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.060
477
BCT004 Bacteriuria 48 0.060
478
P VTR007 Vitreoretinopathy 46 0.060
479
TNS005 Tonsillitis 57 0.060
480
SLC006 Silicosis 56 0.060
481
TRY001 Trypanosomiasis 50 0.060
482
P ATX030 Ataxia-Telangiectasia 83 0.060
483
GRD007 Grade Iii Astrocytoma 59 0.060
484
c ADL017 Adult T-Cell Leukemia 57 0.060
485
P LCH002 Lichen Planus 54 0.060
486
RRD056 Rare Disease in Surgical Orthopedic 28 0.060
487
P CLS010 Cluster Headache 43 0.059
488
THY111 Thyroid Carcinoma, Familial Medullary 67 0.059
489
c PRG018 Paragangliomas 1 57 0.059
490
c WLM018 Wilms Tumor 5 62 0.059
491
P LKD001 Leukodystrophy 59 0.059
492
VSC003 Visceral Leishmaniasis 55 0.059
493
CRT015 Carotid Artery Occlusion 44 0.059
494
AMN001 Amenorrhea 54 0.059
495
LRN003 Learning Disability 49 0.059
496
SLP001 Sleeping Sickness 48 0.059
497
PHR003 Pharyngitis 56 0.058
498
P SLM003 Salmonellosis 54 0.058
499
EXT006 Extrahepatic Cholestasis 40 0.058
500
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.058
501
VGN023 Vaginitis 55 0.057
502
c ACT135 Acute Graft Versus Host Disease 51 0.057
503
NTR046 Neutrophil Migration 50 0.057
504
THY125 Thyroid Gland Medullary Carcinoma 51 0.057
505
c PRG106 Progressive Muscular Dystrophy 33 0.057
506
AMN012 Aminoacidopathies 21 0.057
507
SCC003 Succinic Acidemia 10 0.057
508
ENC005 Encephalomalacia 38 0.057
509
c CHR098 Chronic Pyelonephritis 35 0.057
510
P ANR048 Aniridia 1 63 0.057
511
P PNC025 Panic Disorder 53 0.057
512
ANP008 Anaplastic Oligoastrocytoma 30 0.057
513
ACN002 Acanthosis Nigricans 60 0.056
514
SCH003 Schizophreniform Disorder 56 0.056
515
HSH003 Hashimoto Thyroiditis 62 0.056
516
P MLT074 Multiple Endocrine Neoplasia 55 0.056
517
HML018 Homologous Wasting Disease 22 0.056
518
RTN003 Retinal Ischemia 50 0.056
519
c HMC039 Hemochromatosis, Type 1 74 0.056
520
P ANG015 Angioedema 54 0.056
521
P RTT002 Rett Syndrome 80 0.056
522
PRM329 Premature Aging 39 0.056
523
P TRC086 Trichohepatoenteric Syndrome 1 59 0.056
524
c MCR112 Microvascular Complications of Diabetes 2 41 0.056
525
KRN002 Kearns-Sayre Syndrome 63 0.055
526
ACR007 Acromegaly 71 0.055
527
CMR002 Coumarin Resistance 56 0.055
528
P ASP006 Aspergillosis 66 0.055
529
MSC190 Muscular Disease 51 0.055
530
P RRT020 Rare Tumor 41 0.054
531
GMM004 Gamma-Amino Butyric Acid Metabolism Disorder 27 0.054
532
DFF005 Diffuse Large B-Cell Lymphoma 56 0.054
533
c CNT035 Central Nervous System Disease 54 0.054
534
c GLC092 Glaucoma, Primary Open Angle 62 0.054
535
SPT004 Septic Arthritis 57 0.054
536
CHN010 Chondroma 44 0.054
537
MYP097 Myopathy with Lactic Acidosis, Hereditary 32 0.054
538
LST001 Listeriosis 54 0.054
539
ACT084 Acute Stress Disorder 48 0.054
540
SYS003 Systolic Heart Failure 50 0.053
541
ERL001 Early Myoclonic Encephalopathy 61 0.053
542
BRN002 Bronchiolitis 59 0.053
543
P INT070 Intestinal Obstruction 58 0.053
544
PST028 Post-Traumatic Stress Disorder 58 0.053
545
ORL005 Oral Candidiasis 56 0.053
546
P SNS001 Sensorineural Hearing Loss 61 0.053
547
P BNG030 Benign Ependymoma 60 0.053
548
P VNT002 Ventricular Septal Defect 60 0.053
549
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.053
550
P GNT008 Giant Cell Tumor 44 0.053
551
MCL006 Macular Retinal Edema 55 0.052
552
HRT011 Heart Septal Defect 50 0.052
553
THY124 Thyroid Gland Papillary Carcinoma 52 0.052
554
PPL002 Papillary Carcinoma 47 0.052
555
c ATS347 Autosomal Dominant Polycystic Kidney Disease 59 0.052
556
THR013 Thoracic Outlet Syndrome 53 0.052
557
CLL010 Cellular Ependymoma 53 0.052
558
P CWD010 Cowden Syndrome 66 0.052
559
WST001 West Syndrome 60 0.051
560
SXL003 Sexual Disorder 48 0.051
561
MYF002 Myofascial Pain Syndrome 42 0.051
562
GNG005 Gangliocytoma 55 0.051
563
GNG002 Ganglioneuroma 53 0.051
564
NWB001 Newborn Respiratory Distress Syndrome 58 0.051
565
P RNL015 Renal Hypertension 48 0.051
566
P MTH007 Methemoglobinemia 46 0.051
567
LMB062 Limb Ischemia 55 0.051
568
CLL003 Cellulitis 54 0.051
569
PRS063 Paresthesia 43 0.051
570
P MTC004 Mitochondrial Encephalomyopathy 43 0.050
571
c DFN360 Deafness, Autosomal Dominant 69 37 0.050
572
AND002 Androgen Insensitivity Syndrome 66 0.050
573
P MST009 Mastocytosis 63 0.050
574
TRP009 Triple X Syndrome 42 0.050
575
P CHL002 Childhood Absence Epilepsy 60 0.050
576
CRC014 Carcinoid Tumors, Intestinal 48 0.050
577
GSG001 Gas Gangrene 50 0.050
578
P ANG001 Angelman Syndrome 67 0.049
579
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.049
580
P HMR005 Hemorrhoid 46 0.049
581
MNG007 Manganese Poisoning 29 0.049
582
P MYT002 Myotonic Dystrophy 49 0.049
583
P MGR001 Migraine Without Aura 48 0.049
584
DRG024 Drug Allergy 43 0.049
585
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 37 0.049
586
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 0.049
587
CHL152 Childhood Acute Lymphocytic Leukemia 43 0.048
588
c ACT020 Acute T Cell Leukemia 53 0.048
589
c MCL013 Mucolipidosis Iv 64 0.048
590
ERY003 Erythema Multiforme 57 0.048
591
P HML001 Hemolytic-Uremic Syndrome 52 0.048
592
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.048
593
P MTR003 Mitral Valve Stenosis 50 0.047
594
c ALP101 Alpha-Thalassemia 62 0.047
595
SHG001 Shigellosis 55 0.047
596
OST011 Osteomalacia 52 0.047
597
CRB090 Cerebral Hypoxia 43 0.047
598
ATM052 Autoimmune Disease 1 37 0.047
599
LWC002 Lowe Oculocerebrorenal Syndrome 66 0.047
600
HMP001 Hemopericardium 46 0.047
601
CHL147 Chlamydia Pneumonia 45 0.047
602
CYN002 Cyanosis, Transient Neonatal 45 0.047
603
P CRB088 Cerebral Atrophy 38 0.047
604
ATX010 Ataxia Neuropathy Spectrum 38 0.047
605
ACT064 Acute Necrotizing Encephalitis 32 0.047
606
BLD137 Blood Group--Ahonen 19 0.047
607
MRP001 Morphine Dependence 41 0.047
608
CNV004 Canavan Disease 60 0.046
609
DFF036 Differentiated Thyroid Carcinoma 51 0.046
610
STT002 Status Asthmaticus 49 0.046
611
c PRG020 Paragangliomas 3 38 0.046
612
ALP048 Alopecia Totalis 31 0.046
613
THY006 Thymus Lymphoma 26 0.046
614
CLR030 Clear Cell Renal Cell Carcinoma 53 0.046
615
HRT012 Heart Valve Disease 53 0.046
616
THR016 Thrombophlebitis 51 0.046
617
BLP005 Blepharitis 49 0.046
618
RTC005 Reticulosarcoma 49 0.046
619
c NRF024 Neurofibromatosis, Type I 71 0.045
620
MSN004 Mesenchymal Cell Neoplasm 41 0.045
621
P INB001 Inborn Amino Acid Metabolism Disorder 10 0.045
622
VLV047 Volvulus of Midgut 50 0.045
623
SPT005 Spotted Fever 49 0.045
624
PLS025 Plasmablastic Lymphoma 47 0.045
625
VGN019 Vaginal Discharge 44 0.045
626
P AVS003 Avascular Necrosis 42 0.045
627
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.045
628
c PRG019 Paragangliomas 2 31 0.045
629
P TCD001 Tic Disorder 54 0.045
630
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.045
631
ORL013 Oral Lichen Planus 45 0.045
632
GST020 Gastric Antral Vascular Ectasia 41 0.045
633
LPD012 Lipoid Congenital Adrenal Hyperplasia 71 0.044
634
P EPL140 Epilepsy, Idiopathic Generalized 61 0.044
635
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 49 0.044
636
FMR004 Fumarase Deficiency 41 0.044
637
CHR176 Chromophil Renal Cell Carcinoma 23 0.044
638
P CYS039 Cystic Kidney Disease 54 0.044
639
ACR041 Acromelic Frontonasal Dysostosis 52 0.044
640
CRV040 Cervix Carcinoma 50 0.044
641
c INV001 Invasive Aspergillosis 48 0.044
642
DBT006 Diabetic Macular Edema 48 0.044
643
c BCT013 Bacterial Pneumonia 47 0.044
644
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.044
645
CNN003 Conn's Syndrome 79 0.044
646
RSP019 Respiratory Distress Syndrome in Premature Infants 57 0.044
647
GLL018 Gallbladder Cancer 56 0.044
648
P HYP111 Hyperprolinemia 39 0.044
649
NSP002 Nasopharyngitis 41 0.043
650
GBM001 Gaba Aminotransferase Deficiency 19 0.043
651
CLB002 Clubfoot 47 0.042
652
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.042
653
P AXN002 Axenfeld-Rieger Syndrome 58 0.042
654
SJG002 Sjogren-Larsson Syndrome 57 0.042
655
ARG007 Argininemia 57 0.042
656
URT001 Urethritis 48 0.042
657
INT017 Intestinal Schistosomiasis 47 0.042
658
P SPR086 Spermatogenic Failure 3 44 0.042
659
UND005 Undifferentiated Pleomorphic Sarcoma 66 0.041
660
P EPL198 Epilepsy, Myoclonic Juvenile 62 0.041
661
GNR004 Generalized Anxiety Disorder 56 0.041
662
BRT005 Barth Syndrome 53 0.041
663
EXP004 Exophthalmos 52 0.041
664
OPT003 Opiate Dependence 50 0.041
665
RCK002 Rocky Mountain Spotted Fever 40 0.041
666
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 61 0.041
667
SMN007 Seminoma 44 0.041
668
c CWD006 Cowden Syndrome 1 77 0.041
669
P ALG028 Alagille Syndrome 1 73 0.040
670
ATR057 Atrioventricular Block 55 0.040
671
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.040
672
LNG015 Lingual-Facial-Buccal Dyskinesia 47 0.040
673
ALR002 Al-Raqad Syndrome 34 0.040
674
P PLV020 Pelvic Organ Prolapse 59 0.040
675
BHR001 Behr Syndrome 49 0.040
676
TST015 Testicular Disease 43 0.040
677
P HYP263 Hypersomnia 41 0.040
678
GBT001 Gaba-Transaminase Deficiency 39 0.040
679
P OTT001 Otitis Externa 39 0.040
680
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.040
681
ALP097 Alopecia Universalis Congenita 56 0.039
682
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 58 0.039
683
APH002 Aphasia 57 0.039
684
TNG003 Tongue Cancer 55 0.039
685
APR001 Apraxia 51 0.039
686
HPT082 Hepatic Adenomas, Familial 37 0.039
687
HNM002 Hinman Syndrome 29 0.039
688
c MTC060 Mitochondrial Dna Depletion Syndrome 9 48 0.039
689
ONC007 Oncocytoma 48 0.039
690
c MTR002 Mitral Valve Insufficiency 47 0.039
691
MLN003 Melancholia 39 0.039
692
ART001 Arterial Tortuosity Syndrome 66 0.038
693
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 64 0.038
694
ISL001 Islet Cell Tumor 56 0.038
695
P ALP106 Alport Syndrome 1, X-Linked 55 0.038
696
HMT008 Hematuria, Benign Familial 53 0.038
697
ADR016 Adrenal Cortical Carcinoma 48 0.038
698
ADP007 Adie Pupil 39 0.038
699
VTM028 Vitamin E, Familial Isolated Deficiency of 52 0.038
700
CRR012 Cirrhotic Cardiomyopathy 23 0.038
701
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.038
702
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.038
703
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.038
704
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 39 0.038
705
ADR004 Adrenal Cortical Adenocarcinoma 38 0.038
706
DRM009 Dermatomycosis 36 0.038
707
RSP007 Respiratory Distress Syndrome, Infant 30 0.038
708
LYM053 Lymphomatous Thyroiditis 22 0.037
710
P END047 Endophthalmitis 52 0.037
711
P MGR003 Migraine with Aura 50 0.037
712
P PRT026 Parotitis 42 0.037
713
CVT001 Cavitary Optic Disc Anomalies 38 0.037
714
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.036
715
CHR072 Chordoma 59 0.036
716
P RNL017 Renal Oncocytoma 53 0.036
717
DYS009 Dysthymic Disorder 48 0.036
718
CRN019 Coronary Artery Vasospasm 46 0.036
719
c RNG019 Ring Chromosome 3 21 0.036
720
OBS524 Obsolete: Benign Exophthalmos Syndrome 15 0.036
721
P ACR001 Aicardi-Goutieres Syndrome 65 0.035
722
PNM001 Pneumocystosis 54 0.035
723
c SPN294 Spinocerebellar Ataxia 1 52 0.035
724
c ACR116 Aicardi-Goutieres Syndrome 1 51 0.035
725
APL002 Aplasia of Lacrimal and Salivary Glands 50 0.035
726
SCL003 Social Phobia 48 0.035
727
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 43 0.035
728
BRK012 Broken Heart Syndrome 35 0.035
729
TRC120 Tricarboxylic Acid Cycle, Defect of 16 0.035
730
c MLT160 Multiple Endocrine Neoplasia, Type Iia 69 0.035
731
NRL004 Neuroleptic Malignant Syndrome 55 0.035
732
EPT021 Epithelial Recurrent Erosion Dystrophy 37 0.035
733
PRX097 Paroxysmal Dystonia 31 0.035
734
TST003 Testicular Leukemia 26 0.035
735
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 24 0.035
736
DRG016 Drug Induced Dyskinesia 24 0.035
737
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 67 0.034
738
HMN009 Hemangioblastoma 54 0.034
739
ENC055 Encephalopathy, Ethylmalonic 52 0.034
740
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 50 0.034
741
MNN020 Meningococcal Infection 45 0.034
742
SDD008 Sudden Sensorineural Hearing Loss 43 0.034
744
HYP026 Hypoglycemic Coma 38 0.034
745
HYP189 Hypoadrenalism 37 0.034
746
MYC088 Mycobacterium Avium Complex Infections 29 0.034
747
P MTR012 Mitral Valve Disease 57 0.033
748
P ART018 Aortic Valve Insufficiency 53 0.033
749
P ACT105 Acute Mountain Sickness 52 0.033
750
WRN003 Wernicke Encephalopathy 47 0.033
751
OPD001 Opioid Abuse 45 0.033
752
PNC085 Penicillin Allergy 44 0.033
753
P PHT010 Photoparoxysmal Response 1 42 0.033
754
P MYC026 Myoclonus Epilepsy 35 0.033
755
NRP027 Neuropathy, Painful 24 0.033
756
NCL007 Nuclear Gene-Encoded Leigh Syndrome 23 0.033
758
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.033
759
MNN032 Meningococcal Meningitis 46 0.033
760
DNT006 Dental Pulp Necrosis 40 0.033
761
CRB009 Cerebritis 36 0.033
762
c BLD140 Blood Group, I System 30 0.033
763
DFF015 Diffuse Glomerulonephritis 27 0.033
764
AND005 Androgen Insensitivity Syndrome, Mild 22 0.033
765
HYP780 Hypoadrenocorticism, Familial 62 0.031
766
P OST009 Osteochondritis Dissecans 60 0.031
767
P JVN007 Juvenile Absence Epilepsy 48 0.031
768
MCR037 Macroglossia 45 0.031
769
URN003 Urinary Schistosomiasis 44 0.031
770
ADR041 Adrenal Cortical Adenoma 43 0.031
771
BSL008 Basal Ganglia Disease 43 0.031
772
PTY002 Pityriasis Versicolor 37 0.031
773
PRS025 Presbyopia 37 0.031
774
P BCL013 B-Cell Adult Acute Lymphocytic Leukemia 32 0.031
775
ACT216 Acute Leukemia of Ambiguous Lineage 32 0.031
776
FCL001 Facial Dermatosis 29 0.031
777
WLM014 Wilms Tumor, Aniridia, Genitourinary Anomalies, and Mental Retardation Syndrome 49 0.031
778
FML304 Familial Isolated Dilated Cardiomyopathy 40 0.031
779
c MLG157 Malignant Pheochromocytoma 39 0.031
780
WLM019 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome 17 0.031
781
CHR001 Churg-Strauss Syndrome 60 0.030
782
P CRN028 Corneal Ulcer 47 0.030
783
c CHR095 Chronic Progressive External Ophthalmoplegia 46 0.030
784
c EPL133 Epilepsy, Juvenile Absence 1 39 0.030
785
GLT028 Glutaric Aciduria Iii 28 0.030
786
ALL012 Allergic Angiitis 24 0.030
787
P CNG499 Congenital Anomalies of Kidney and Urinary Tract 2 49 0.029
788
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 43 0.029
789
P CRB045 Cerebellar Hypoplasia 37 0.029
790
P SYR003 Syringoma 37 0.029
791
c GST103 Gastric Cancer, Hereditary Diffuse 64 0.028
792
P DYS193 Dystonia 11, Myoclonic 56 0.028
793
c VRL005 Viral Pneumonia 49 0.028
794
P PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 48 0.028
795
P CPL014 Capillary Malformation-Arteriovenous Malformation 1 47 0.028
796
c ATM092 Autoimmune Polyendocrine Syndrome, Type Ii 46 0.028
797
c HYP793 Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 44 0.028
798
c PRG039 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 44 0.028
799
c PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 42 0.028
800
P CRN035 Cranial Nerve Palsy 41 0.028
801
c PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 40 0.028
802
TST043 Testicular Seminoma 35 0.028
803
FMR011 Fumarate Hydratase Deficiency 30 0.028
804
P JBR020 Joubert Syndrome 1 72 0.026
805
MLT163 Multiple Pterygium Syndrome, Escobar Variant 64 0.026
806
P CHR640 Charcot-Marie-Tooth Disease, X-Linked Dominant, 1 56 0.026
807
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 56 0.026
808
CLL002 Collecting Duct Carcinoma 54 0.026
809
SPS007 Spastic Cerebral Palsy 45 0.026
810
EMP001 Empty Sella Syndrome 44 0.026
811
c XLN110 X-Linked Charcot-Marie-Tooth Disease 43 0.026
812
ANG011 Angiodysplasia 43 0.026
813
PSD001 Pseudobulbar Palsy 40 0.026
814
MCC013 Mucocutaneous Ulceration, Chronic 39 0.026
815
SCL001 Scalp Dermatosis 37 0.026
816
CNT001 Contagious Pustular Dermatitis 29 0.026
817
LKN027 Leukoencephalopathy, Acute Reversible, with Increased Urinary Alpha-Ketoglutarate 18 0.026
818
WLL001 Williams-Beuren Syndrome 62 0.024
819
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 59 0.024
820
c CTS029 Cutis Laxa, Autosomal Recessive, Type Iiia 54 0.024
821
HYP134 Hypoparathyroidism-Retardation-Dysmorphism Syndrome 52 0.024
822
FCL022 Focal Dystonia 42 0.024
823
MRN002 Mooren's Ulcer 38 0.024
824
HRM003 Hormone Producing Pituitary Cancer 37 0.024
825
PHT003 Phototoxic Dermatitis 34 0.024
826
INT040 Intrinsic Asthma 34 0.024
827
PRN007 Perinephritis 33 0.024
828
c INF086 Inflammatory Bowel Disease 3 32 0.024
829
c SPR094 Sporadic Pheochromocytoma 32 0.024
830
CTC004 Catecholamine-Producing Tumor 30 0.024
831
MSC004 Muscle Tissue Disease 25 0.024
832
HND001 Hand Dermatosis 22 0.024
833
CHL135 Chloramphenicol Toxicity 18 0.024
834
STN005 St Anthony's Fire 17 0.024
Content
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