Search results for NADH

1236 hits were found for NADH

# Family MCID Name MIFTS Score
1
MTH026 Methemoglobinemia Due to Deficiency of Methemoglobin Reductase 36 42.250
2
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 59 38.963
3
P MPL001 Maple Syrup Urine Disease 69 9.403
4
DHY010 Dihydrolipoamide Dehydrogenase Deficiency 48 9.289
5
PYR031 Pyruvate Dehydrogenase E3-Binding Protein Deficiency 43 9.197
6
P MTH007 Methemoglobinemia 46 6.746
7
c CNG223 Congenital Methemoglobinemia 39 5.883
8
ANX004 Anoxia 40 4.193
9
P MYP004 Myopathy 67 3.636
10
P OPT006 Optic Nerve Disease 57 3.310
11
P LCT001 Lactic Acidosis 50 3.301
12
P HRD217 Hereditary Optic Neuropathy 36 3.292
13
MTC005 Mitochondrial Metabolism Disease 44 3.215
14
P MTC133 Mitochondrial Myopathy 51 3.085
15
P NRP001 Neuropathy 59 2.804
16
LBR038 Leber Hereditary Optic Neuropathy, Modifier of 62 2.800
17
CYN002 Cyanosis, Transient Neonatal 43 2.751
18
HYP266 Hypoxia 56 2.593
19
P MTC069 Mitochondrial Disorders 57 2.525
20
P PRK039 Parkinsonism 55 2.485
21
LGH007 Leigh Syndrome 70 2.415
22
CHR066 Chronic Fatigue Syndrome 59 2.375
23
HLX001 Helix Syndrome 47 2.285
24
P NRB001 Neuroblastoma 66 2.107
25
FTT001 Fatty Liver Disease 61 2.010
26
CHG001 Chagas Disease 65 1.985
27
MTC004 Mitochondrial Encephalomyopathy 42 1.956
28
P MYC084 Mycobacterium Tuberculosis 1 68 1.938
29
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 1.927
30
SCC003 Succinic Acidemia 10 1.918
31
LBR036 Leber Plus Disease 67 1.901
32
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 1.891
33
c ATR087 Atrial Standstill 1 74 1.883
34
P ENC018 Encephalopathy 62 1.875
35
GLL048 Glial Tumor 51 1.875
36
HYP066 Hyperglycemia 60 1.778
37
GLM045 Glioma 62 1.746
38
P ALZ034 Alzheimer Disease 87 1.715
39
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 62 1.704
40
CHL014 Cholera 62 1.704
41
LPD008 Lipid Metabolism Disorder 61 1.697
42
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 44 1.680
43
AGN016 Aging 53 1.648
44
CYS001 Cystic Fibrosis 77 1.599
45
PRT037 Pertussis 49 1.549
46
HYP056 Hypoglycemia 65 1.536
47
MTH072 Methemoglobin Reductase Deficiency 15 1.524
48
BRN071 Brain Injury 50 1.449
49
P HYP061 Hypertrophic Cardiomyopathy 68 1.424
50
P KLZ004 Kala-Azar 1 41 1.392
51
IRN002 Iron Metabolism Disease 56 1.392
52
LSH001 Leishmaniasis 63 1.392
53
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.390
54
P GST053 Gastric Cancer 82 1.389
55
P DYS154 Dystonia 64 1.383
56
TRM010 Traumatic Brain Injury 50 1.383
57
HMP009 Haemophilus Influenzae 41 1.374
58
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.356
59
c MJR022 Major Affective Disorder 8 37 1.326
60
c MJR024 Major Affective Disorder 9 40 1.326
61
P BPL003 Bipolar Disorder 56 1.326
62
P HYP265 Hypotonia 42 1.321
63
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.306
64
c MCR115 Microvascular Complications of Diabetes 5 65 1.283
65
P CHR012 Chronic Granulomatous Disease 69 1.275
66
DYS015 Dysentery 49 1.273
67
ART140 Arteries, Anomalies of 52 1.261
68
LPP008 Lipoprotein Quantitative Trait Locus 65 1.261
69
P BRS047 Breast Cancer 97 1.251
70
P VSC007 Vascular Disease 62 1.249
71
CRN030 Coronary Stenosis 50 1.249
72
ECH003 Echinococcosis 52 1.247
73
ATS010 Autosomal Recessive Disease 42 1.236
74
OST159 Osteogenic Sarcoma 66 1.226
75
P PRK057 Parkinson Disease, Late-Onset 79 1.226
76
P HNT016 Huntington Disease 73 1.217
77
CRT020 Cortisone Reductase Deficiency 36 1.211
78
GLB002 Glioblastoma 67 1.199
79
HRW001 Hair Whorl 35 1.160
80
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 1.160
81
RNL114 Renal Cell Carcinoma, Nonpapillary 79 1.150
82
P SZR006 Seizure Disorder 69 1.150
83
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.140
84
PST092 Posttransplant Acute Limbic Encephalitis 29 1.140
85
c BRN108 Branchiootic Syndrome 1 63 1.118
86
DNT012 Dental Caries 53 1.118
87
MTB004 Metabolic Acidosis 48 1.112
88
P SPP010 Suppressor of Tumorigenicity 3 50 1.107
89
P CTR002 Cataract 59 1.107
90
48X005 48,xyyy 39 1.097
91
SLP001 Sleeping Sickness 56 1.095
92
P MSC005 Muscular Dystrophy 66 1.090
93
MLR004 Malaria 77 1.083
94
P RSP003 Respiratory Failure 73 1.083
95
ALL014 Allergic Encephalomyelitis 34 1.083
96
CTR172 Citrullinemia, Classic 64 1.075
97
CRT015 Carotid Artery Occlusion 45 1.067
98
P BRS044 Breast Adenocarcinoma 58 1.057
99
CRB004 Cerebral Artery Occlusion 45 1.051
100
P INF032 Infertility 60 1.030
101
PRM329 Premature Aging 36 1.030
102
P MYP087 Myopathy, Tubular Aggregate, 1 49 1.025
103
CNT047 Contact Dermatitis 56 1.015
104
ALC007 Alcohol Dependence 65 1.010
105
c DLT002 Dilated Cardiomyopathy 79 1.001
106
c THY056 Thyroid Dyshormonogenesis 3 32 0.999
107
CHL065 Cholangiocarcinoma 57 0.999
108
TRN015 Transient Cerebral Ischemia 62 0.999
109
INT079 Intrahepatic Cholangiocarcinoma 51 0.999
110
P MSC003 Muscular Atrophy 52 0.992
111
LCT008 Lactate Dehydrogenase Deficiency 14 0.986
112
NRM005 Neuromuscular Disease 62 0.983
113
DRM006 Dermatitis 61 0.982
114
CRV040 Cervix Carcinoma 50 0.982
115
KRN002 Kearns-Sayre Syndrome 62 0.973
116
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.964
117
P LTR001 Lateral Sclerosis 57 0.964
118
HYP060 Hyperinsulinism 53 0.954
119
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.944
120
CRB037 Cerebral Palsy 66 0.944
121
PST011 Pustulosis of Palm and Sole 52 0.944
122
GRD001 Giardiasis 46 0.944
123
P PSR002 Psoriasis 63 0.944
124
c HPT001 Hepatitis C 61 0.944
125
STN013 Stenotrophomonas Maltophilia Infection 26 0.944
126
P PHC003 Pheochromocytoma 70 0.934
127
CNG393 Congenital Muscular Dystrophy with Hyperlaxity 12 0.934
128
P ATS364 Autism 72 0.924
129
c HPT073 Hepatitis C Virus 70 0.924
130
c HYP836 Hypercholesterolemia, Familial, 1 73 0.913
131
ORL011 Oral Cancer 60 0.913
132
SQM006 Squamous Cell Carcinoma 59 0.902
133
RBF001 Riboflavin Deficiency 49 0.898
134
GLC003 Glucose Intolerance 53 0.891
135
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.891
136
CRB090 Cerebral Hypoxia 42 0.891
137
ATH013 Atherosclerosis Susceptibility 63 0.879
138
c HYP595 Hypertension, Essential 84 0.879
139
P MCR010 Microcephaly 59 0.879
140
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 24 0.879
141
URT049 Urate Oxidase, Pseudogene 24 0.867
142
P LPR021 Leprosy 3 71 0.867
143
HNS001 Hansen's Disease 32 0.867
144
CND006 Candida Glabrata 29 0.867
145
MYP161 Myopathy, Congenital Proximal, with Minicore Lesions 17 0.856
146
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.854
147
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.854
148
HYP014 Hyperuricemia 51 0.854
149
c CHR095 Chronic Progressive External Ophthalmoplegia 48 0.854
150
KRT002 Keratomalacia 54 0.841
151
P CRD119 Cardiac Arrest 68 0.841
152
P MLT020 Multiple Sclerosis 79 0.841
153
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.841
154
HMC014 Homocysteinemia 52 0.841
155
P LPS004 Lupus Erythematosus 61 0.841
156
P MYC033 Myoclonus 46 0.841
157
c SPR009 Sporadic Breast Cancer 42 0.830
158
ORL015 Oral Squamous Cell Carcinoma 43 0.828
159
c SYS001 Systemic Lupus Erythematosus 85 0.828
160
P PRS040 Prostate Cancer 95 0.828
161
P PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 54 0.828
162
CRV035 Cervical Cancer 72 0.828
163
P FBR017 Fibrosarcoma 55 0.828
164
P THL005 Thalassemia 56 0.828
165
HDN002 Head Injury 44 0.828
166
P PTS002 Ptosis 52 0.813
167
P SCH015 Schizophrenia 74 0.813
168
c LKM061 Leukemia, Acute Myeloid 83 0.813
169
ART002 Arts Syndrome 66 0.813
170
c PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 49 0.813
171
c PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 52 0.813
172
P ANP001 Anaplastic Large Cell Lymphoma 59 0.813
173
c ACT068 Acute Cystitis 60 0.813
174
TTN003 Tetanus 64 0.813
175
SPS057 Spasticity 43 0.813
176
c HYP807 Hyperinsulinemic Hypoglycemia, Familial, 6 52 0.798
177
OCL069 Ocular Motor Apraxia 57 0.798
178
SCK003 Sickle Cell Anemia 74 0.798
179
P EXN002 Exanthem 58 0.798
180
VLV047 Volvulus of Midgut 55 0.798
181
P MYC008 Myocarditis 59 0.798
182
DBT084 Diabetes Mellitus, Ketosis-Prone 59 0.783
183
P FRD001 Friedreich Ataxia 62 0.783
184
INT071 Intestinal Perforation 49 0.783
185
P CRV031 Cervical Adenocarcinoma 48 0.783
186
ACT098 Acute Erythroid Leukemia 55 0.783
187
INS001 Insulinoma 59 0.783
188
P GST044 Gastritis 55 0.783
189
FLR002 Filariasis 55 0.783
190
ALV002 Alveolar Echinococcosis 56 0.783
191
P MLG056 Malignant Hyperthermia 65 0.783
192
c MGR028 Migraine with or Without Aura 1 63 0.766
193
OTT002 Otitis Media 70 0.766
194
P BLD134 Bladder Cancer 79 0.766
195
HGH043 High Grade Glioma 46 0.766
196
c PRC016 Pre-Eclampsia 64 0.766
197
P MYL006 Myeloid Leukemia 60 0.766
198
LTH004 Lathyrism 15 0.766
199
INS024 Insulin-Like Growth Factor I 77 0.748
200
P LNG032 Lung Cancer 98 0.748
201
ONC002 Onchocerciasis 50 0.748
202
PRM236 Primary Biliary Cholangitis 62 0.748
203
RSC001 Rosacea 55 0.748
204
VSC003 Visceral Leishmaniasis 54 0.748
205
PTH003 Pathologic Nystagmus 52 0.748
206
c RNG015 Ring Chromosome 2 22 0.748
207
DYS073 Dysphagia 53 0.748
208
INF034 Infective Endocarditis 53 0.728
209
PRT251 Proteinuria, Chronic Benign 58 0.728
210
RTN212 Retinal Dystrophy with or Without Macular Staphyloma 31 0.728
211
MSC007 Muscle Hypertrophy 64 0.728
212
c THY071 Thyroid Dyshormonogenesis 1 31 0.728
213
CHL123 Chlamydia 58 0.728
214
P BNG032 Benign Mesothelioma 53 0.728
215
P ECL001 Eclampsia 52 0.728
216
CLR030 Clear Cell Renal Cell Carcinoma 53 0.728
217
P END033 Endocarditis 58 0.728
218
P PRP029 Porphyria 60 0.728
219
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.728
220
P CCK001 Cockayne Syndrome 67 0.728
221
P MTH008 Methylmalonic Acidemia 52 0.728
222
ISL099 Isolated Methylmalonic Acidemia 35 0.728
223
PRT036 Peritonitis 65 0.728
224
CYN003 Cyanide Poisoning 22 0.728
225
RHB024 Rhabdomyosarcoma 2 65 0.711
226
HYP781 Hypoascorbemia 52 0.711
227
ANT039 Antisynthetase Syndrome 55 0.711
228
FST001 Foster-Kennedy Syndrome 39 0.711
229
ORG002 Organic Acidemia 43 0.706
230
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.706
231
PRP027 Peripheral Vascular Disease 71 0.706
232
ANG054 Angina Pectoris 65 0.706
233
MST004 Mast Cell Neoplasm 41 0.706
234
EXT007 Extracutaneous Mastocytoma 38 0.706
235
P HRD018 Hair Disease 43 0.706
236
HLL004 Hellp Syndrome 53 0.706
237
ISC004 Ischemia 61 0.683
238
DWN001 Down Syndrome 70 0.682
239
MNK001 Menkes Disease 64 0.682
240
LBR031 Leber Optic Atrophy and Dystonia 39 0.682
241
BRK010 Burkitt Lymphoma 65 0.682
242
ESP021 Esophageal Cancer 84 0.682
243
P LRY044 Larynx Cancer 53 0.682
244
P HPT021 Hepatitis 68 0.682
245
LYD001 Leydig Cell Tumor 45 0.682
246
P HYD006 Hydrocephalus 62 0.682
247
CRB039 Cerebrovascular Disease 65 0.682
248
PRX097 Paroxysmal Dystonia 32 0.682
249
HMM004 Hamamy Syndrome 39 0.652
250
SNG007 Sengers Syndrome 45 0.652
251
PLT031 Platelet Membrane Fluidity 28 0.652
252
KRT058 Keratoderma, Palmoplantar, with Deafness 42 0.652
253
MYL069 Myeloma, Multiple 76 0.652
254
P DFN349 Deafness, Nonsyndromic Sensorineural, Mitochondrial 35 0.652
255
CNR001 Coenurosis 26 0.652
256
PRS119 Persistent Genital Arousal Disorder 18 0.652
257
ANS011 Anus Cancer 55 0.652
258
SVR001 Severe Acute Respiratory Syndrome 68 0.652
259
ALL010 Allergic Contact Dermatitis 55 0.652
260
P GRV001 Graves' Disease 54 0.652
261
TNS005 Tonsillitis 57 0.652
262
P BRN006 Branchiootorenal Syndrome 51 0.652
263
SCR011 Scrapie 39 0.652
264
NNS010 Nonsyndromic Hearing Loss and Deafness, Mitochondrial 13 0.652
265
PRS034 Parasitic Helminthiasis Infectious Disease 50 0.652
266
P RRT020 Rare Tumor 39 0.652
267
EST002 Estrogen-Receptor Negative Breast Cancer 45 0.614
268
APR001 Apraxia 51 0.614
269
ARG002 Argininosuccinic Aciduria 61 0.614
270
P MCH002 Machado-Joseph Disease 62 0.614
271
ALZ029 Alzheimer Disease Mitochondrial 24 0.614
272
SPS007 Spastic Cerebral Palsy 45 0.614
273
ASP002 Aspartylglucosaminuria 57 0.614
274
HYP690 Hyper-Beta-Alaninemia 24 0.614
275
PNB004 Panbronchiolitis, Diffuse 34 0.614
276
PTN001 Patent Foramen Ovale 61 0.614
277
P DRR001 Diarrhea 55 0.614
278
P BLD062 Bile Duct Cancer 69 0.614
279
P DBT005 Diabetes Insipidus 54 0.614
280
CYS008 Cystic Echinococcosis 57 0.604
281
P CTR177 Citrullinemia, Type Ii, Adult-Onset 56 0.583
282
CHL068 Cholestasis 61 0.560
283
P MLN008 Melanoma 75 0.553
284
c ALP101 Alpha-Thalassemia 62 0.522
285
P DRM053 Dermatitis, Atopic 65 0.522
286
c LCT020 Lactic Acidosis, Chronic Adult Form 8 0.522
288
P LVR013 Liver Disease 68 0.521
289
P SCK005 Sickle Cell Disease 56 0.470
290
c MCR133 Microvascular Complications of Diabetes 4 41 0.461
291
c MCR113 Microvascular Complications of Diabetes 3 52 0.461
292
c MCR130 Microvascular Complications of Diabetes 6 41 0.461
293
c MCR120 Microvascular Complications of Diabetes 7 47 0.461
294
P PLM037 Pulmonary Hypertension 69 0.442
295
DBT010 Diabetic Neuropathy 54 0.442
296
47X002 47,xyy 47 0.432
297
PPL052 Papillomatosis, Confluent and Reticulated 34 0.422
298
STT001 Status Epilepticus 58 0.412
299
TXC005 Toxic Shock Syndrome 61 0.412
300
P PRD008 Periodontitis 63 0.412
301
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 41 0.402
302
c TYP009 Type 2 Diabetes Mellitus 91 0.402
303
c ACT071 Acute Kidney Failure 60 0.402
304
PHN003 Phenylketonuria 76 0.391
305
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.380
306
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.380
307
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.380
308
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.380
309
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.380
310
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.380
311
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 0.380
312
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.380
313
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.380
314
ADR040 Adrenal Gland Pheochromocytoma 45 0.380
315
P SKN015 Skin Carcinoma 71 0.380
316
P BCL017 B-Cell Lymphoma 57 0.380
318
P GLC113 Galactosemia I 65 0.369
319
HPT022 Hepatoblastoma 54 0.369
320
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 0.357
321
P LNG064 Lung Cancer Susceptibility 3 69 0.357
322
CNG034 Congestive Heart Failure 69 0.357
323
HRT015 Heritable Pulmonary Arterial Hypertension 46 0.357
324
P TRM003 Tremor 50 0.357
325
c TYP008 Type 1 Diabetes Mellitus 77 0.345
326
BRN004 Brain Edema 54 0.345
327
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 0.332
328
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.332
329
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.332
330
BCT022 Bacterial Infectious Disease 55 0.332
331
P BRG001 Brugada Syndrome 69 0.319
332
MTH071 Methane Production 24 0.319
333
CYS005 Cysticercosis 60 0.319
334
ARG004 Argyria 26 0.319
335
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.306
336
c SPR086 Spermatogenic Failure 3 47 0.306
337
P LKM002 Leukemia 65 0.306
338
HMS001 Hemosiderosis 48 0.306
339
c ACT027 Acute Pancreatitis 60 0.306
340
SCH014 Schistosomiasis 56 0.306
341
P HML002 Hemolytic Anemia 62 0.306
342
BRN056 Bronchopulmonary Dysplasia 57 0.306
343
c CHR684 Chronic Kidney Disease 73 0.306
344
P HYP076 Hyperthyroidism 53 0.306
345
P RRH023 Rare Hereditary Hemochromatosis 52 0.306
346
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.291
347
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.291
348
DSS032 Disease by Infectious Agent 55 0.291
349
P PNC035 Pancreatic Cancer 87 0.291
350
P ALC033 Alcohol Use Disorder 67 0.291
351
P DBT009 Diabetes Mellitus 67 0.291
352
P OVR042 Ovarian Cancer 88 0.276
353
P CLR023 Colorectal Cancer 100 0.276
354
c THY107 Thymoma, Familial 42 0.276
355
c DVL036 Developmental and Epileptic Encephalopathy 39 39 0.276
356
P HPT023 Hepatocellular Carcinoma 95 0.276
357
ONC007 Oncocytoma 49 0.276
358
P MYG005 Myoglobinuria 40 0.276
359
DPH001 Diphtheria 59 0.276
360
HPT019 Hepatic Encephalopathy 59 0.276
361
P THY023 Thymoma 64 0.276
362
P MLN007 Male Infertility 56 0.276
363
P PRP019 Peripheral Nervous System Disease 57 0.276
364
P HRT032 Heart Disease 84 0.276
365
LKS001 Leukostasis 40 0.276
366
HPT004 Hepatic Coma 43 0.276
367
P SCL018 Scoliosis 57 0.261
368
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.261
369
BRT005 Barth Syndrome 55 0.261
370
ACR009 Acromesomelic Dysplasia, Hunter-Thompson Type 41 0.261
371
RCH002 Richards-Rundle Syndrome 31 0.261
372
P LKM062 Leukemia, Acute Lymphoblastic 69 0.261
373
P GLY013 Glycogen Storage Disease 59 0.261
374
P BRB001 Beriberi 44 0.261
375
ADN018 Adenoma 58 0.261
376
P ADN016 Adenocarcinoma 63 0.261
377
SPN035 Spindle Cell Sarcoma 51 0.261
378
PLC005 Placental Insufficiency 55 0.261
379
MLT006 Multidrug-Resistant Tuberculosis 47 0.261
380
SRC014 Sarcoma 64 0.261
381
YLL002 Yellow Fever 61 0.261
382
END086 End Stage Renal Disease 54 0.261
383
P INS002 in Situ Carcinoma 52 0.261
384
THY029 Thyroid Carcinoma 55 0.261
385
P APL001 Aplastic Anemia 72 0.244
386
c L2H001 L-2-Hydroxyglutaric Aciduria 49 0.244
387
BTT016 Batten-Turner Congenital Myopathy 54 0.244
389
c 2HY001 2-Hydroxyglutaric Aciduria 38 0.244
390
P RTN008 Retinitis Pigmentosa 79 0.244
392
c OPT053 Optic Atrophy 1 62 0.244
393
c CHL116 Cholestasis, Intrahepatic, of Pregnancy, 1 52 0.244
394
P SNS001 Sensorineural Hearing Loss 60 0.244
395
TRY001 Trypanosomiasis 50 0.244
396
P RNV001 Renovascular Hypertension 48 0.244
397
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.244
398
P BRS053 Breast Fibroadenoma 48 0.244
399
P MVM001 Movement Disease 61 0.244
400
MDD018 Middle East Respiratory Syndrome 44 0.244
401
NRR001 Neuroretinitis 42 0.244
402
P ADL010 Adult Respiratory Distress Syndrome 70 0.244
403
P CNT004 Centronuclear Myopathy 56 0.244
404
RTN023 Retinitis 45 0.244
405
SKN016 Skin Disease 63 0.244
406
P RTN016 Retinal Degeneration 52 0.244
407
c ACT134 Acute Liver Failure 57 0.244
408
DFC004 Deficiency Anemia 74 0.226
409
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.226
410
c PRM108 Primary Progressive Multiple Sclerosis 51 0.226
411
RNL077 Renal Fibrosis 46 0.226
412
MSC157 Muscular Dystrophy, Duchenne Type 78 0.226
413
STR067 Stroke, Ischemic 79 0.226
414
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.226
415
c PCH010 Pachyonychia Congenita 3 43 0.226
416
P ASP006 Aspergillosis 71 0.226
417
P MYS005 Myositis 55 0.226
418
P GLM040 Glioma Susceptibility 1 70 0.226
419
P PLY041 Polymyositis 58 0.226
420
MLG169 Malignant Astrocytoma 57 0.226
421
VCC001 Vaccinia 49 0.226
422
CCC002 Coccidiosis 50 0.226
423
DBT007 Diabetic Cataract 36 0.226
424
LVR012 Liver Cirrhosis 62 0.226
425
GST045 Gastroenteritis 58 0.226
426
P HYP086 Hypothyroidism 68 0.226
427
P CND004 Candidiasis 57 0.226
428
P KDN017 Kidney Cancer 60 0.226
429
CNS004 Constipation 56 0.226
430
ERL001 Early Myoclonic Encephalopathy 62 0.226
431
PSY004 Psychotic Disorder 66 0.226
432
ALC006 Alcoholic Hepatitis 61 0.226
433
RCK004 Rickets 64 0.226
434
P DRM010 Dermatomyositis 61 0.226
435
TLN003 Telangiectasis 51 0.226
436
P RBL001 Rubella 58 0.226
437
STM007 Stomatitis 52 0.226
438
IDP022 Idiopathic Spinal Cord Herniation 17 0.226
439
INT075 Intracranial Hypertension 52 0.226
440
c ATS007 Autism Spectrum Disorder 71 0.206
441
CLT003 Colitis 63 0.206
442
P INF037 Inflammatory Bowel Disease 53 0.206
443
PLY150 Polykaryocytosis Inducer 29 0.206
444
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.206
445
P ATX030 Ataxia-Telangiectasia 80 0.206
446
FRN006 Frontotemporal Dementia 68 0.206
447
HMN044 Human Immunodeficiency Virus Type 1 76 0.206
448
PRS129 Prostatic Hyperplasia, Benign 48 0.206
449
FCL014 Focal Epilepsy 53 0.206
450
P ART021 Arteriosclerosis 53 0.206
451
c BSL007 Basal Cell Carcinoma 67 0.206
452
STR103 Streptococcus Pneumonia 47 0.206
453
PRP016 Paraplegia 52 0.206
454
SVR004 Severe Combined Immunodeficiency 70 0.206
455
LYM017 Lyme Disease 63 0.206
456
CRN019 Coronary Artery Vasospasm 47 0.206
457
P OVR049 Ovarian Disease 50 0.206
458
PRS021 Prostatic Adenoma 43 0.206
459
P RNL015 Renal Hypertension 45 0.206
460
PRS045 Prostatic Hypertrophy 53 0.206
461
P RNL017 Renal Oncocytoma 54 0.206
462
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.206
463
CHL045 Choline Deficiency Disease 39 0.206
464
P TXP001 Toxoplasmosis 59 0.206
465
P HYP098 Hypereosinophilic Syndrome 66 0.206
466
WLL004 Wallerian Degeneration 38 0.206
467
MYC005 Myocardial Stunning 45 0.206
468
P MRC003 Mercury Poisoning 48 0.206
469
MYC015 Mycobacterium Fortuitum 28 0.206
470
P MYC026 Myoclonus Epilepsy 35 0.206
471
IDP070 Idiopathic Scoliosis 41 0.184
472
P CRN300 Coronary Heart Disease 1 73 0.184
473
P SLP006 Sleep Apnea 69 0.184
474
VRC005 Varicose Veins 59 0.184
475
ADR007 Adrenoleukodystrophy 73 0.184
476
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.184
477
c ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.184
478
FML037 Female Breast Cancer 51 0.184
479
c HYP368 Hyperphenylalaninemia, Bh4-Deficient, C 35 0.184
480
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 50 0.184
481
MNN043 Meningioma, Familial 79 0.184
482
ATM095 Autoimmune Disease 61 0.184
483
HLC007 Helicobacter Pylori Infection 67 0.184
484
P BND020 Bone Disease 60 0.184
485
CHK001 Chikungunya 60 0.184
486
P MYS079 Miyoshi Muscular Dystrophy 53 0.184
487
FML035 Familial Hyperlipidemia 54 0.184
488
NNL006 Non-Alcoholic Steatohepatitis 54 0.184
489
TTH006 Tooth Disease 51 0.184
490
CLN015 Colon Adenocarcinoma 64 0.184
491
P PRM002 Primary Hyperoxaluria 65 0.184
492
TRC003 Trichomoniasis 53 0.184
493
KRT009 Keratosis 52 0.184
494
P SPN046 Spinal Muscular Atrophy 62 0.184
495
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.184
496
P EYD002 Eye Disease 57 0.184
497
P KDN018 Kidney Disease 71 0.184
498
P PLY011 Polycystic Ovary Syndrome 57 0.184
499
P URN019 Urinary Tract Infection 48 0.184
500
P OBS001 Obstructive Jaundice 49 0.184
501
HMG005 Hemoglobinopathy 55 0.184
502
SCR001 Secretory Meningioma 40 0.184
503
P PLM036 Pulmonary Fibrosis 65 0.184
504
P PTT006 Pituitary Adenoma 55 0.184
505
P RHB003 Rhabdomyosarcoma 66 0.184
506
ART016 Aortic Aneurysm 68 0.184
507
P PNC044 Pancreatitis 61 0.184
508
GLC008 Glucose Metabolism Disease 40 0.184
509
P CHR071 Charcot-Marie-Tooth Disease 64 0.184
510
INT395 Intracranial Meningioma 47 0.184
511
P CRD246 Cardiovascular System Disease 55 0.184
512
P KRT007 Keratoconus 49 0.184
513
P PRN023 Prion Disease 60 0.184
514
CHR074 Choriocarcinoma 46 0.184
515
FSC002 Fascioliasis 43 0.184
516
GSG001 Gas Gangrene 52 0.184
517
HYP141 Hyperphenylalaninemia 42 0.184
518
P MYT002 Myotonic Dystrophy 51 0.184
519
ADR022 Adrenomyeloneuropathy 38 0.184
520
ULC004 Ulcerative Colitis 74 0.184
521
c ACT075 Acute Myocardial Infarction 55 0.184
522
LNG099 Lung Disease 62 0.184
524
FST010 Fasting Hypoglycemia 33 0.184
525
NCL011 Nuclear Gene-Encoded Leigh Syndrome Spectrum 21 0.184
526
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 0.184
527
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 0.184
528
RHM034 Rahman Syndrome 37 0.160
529
MTC029 Mitochondrial Complex V Deficiency, Nuclear Type 1 40 0.160
530
P MTR004 Maturity-Onset Diabetes of the Young 66 0.160
531
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.160
532
ACH004 Achondroplasia 65 0.160
533
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.160
534
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.160
535
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 53 0.160
536
P SCL057 Scoliosis, Isolated 1 40 0.160
537
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.160
538
P RTT002 Rett Syndrome 79 0.160
539
WRN002 Wernicke-Korsakoff Syndrome 49 0.160
540
MHR001 Mohr-Tranebjaerg Syndrome 49 0.160
541
c HYP602 Hyperoxaluria, Primary, Type Ii 51 0.160
542
TRD006 Tardive Dyskinesia 53 0.160
543
DBT090 Diabetes and Deafness, Maternally Inherited 44 0.160
544
HYP814 Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency 34 0.160
545
c MSC106 Mosaic Variegated Aneuploidy Syndrome 2 41 0.160
546
MTC205 Mitochondrial Complex Iv Deficiency, Nuclear Type 1 57 0.160
547
DGL002 D-Glyceric Aciduria 40 0.160
548
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.160
549
c GLL024 Gallbladder Disease 1 53 0.160
550
P DNG005 Dengue Virus 55 0.160
551
INC002 Inclusion Body Myositis 56 0.160
552
CMR002 Coumarin Resistance 59 0.160
553
FRC013 Fructose Utilization 15 0.160
554
DFF005 Diffuse Large B-Cell Lymphoma 55 0.160
555
INV001 Invasive Aspergillosis 48 0.160
556
c PRG106 Progressive Muscular Dystrophy 31 0.160
557
MLD018 Mild Cognitive Impairment 48 0.160
558
LMB062 Limb Ischemia 55 0.160
559
GST023 Gastric Ulcer 52 0.160
560
SKN005 Skin Atrophy 41 0.160
561
NRT004 Neuritis 53 0.160
562
GLN002 Glanders 38 0.160
563
NRT001 Neurotic Disorder 56 0.160
564
OVR063 Overnutrition 42 0.160
565
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.160
566
P PLY019 Polyneuropathy 52 0.160
567
P GLM007 Glomerulonephritis 59 0.160
568
c HPT016 Hepatitis B 62 0.160
569
P BNG002 Benign Meningioma 36 0.160
570
CRC021 Carcinosarcoma 62 0.160
571
PNC129 Pancreatic Adenocarcinoma 64 0.160
572
ANV001 Anovulation 46 0.160
573
DMY004 Demyelinating Disease 50 0.160
574
MDD011 Mood Disorder 61 0.160
575
URM002 Uremia 47 0.160
576
ALL029 Allergic Disease 61 0.160
577
GST033 Gestational Diabetes 60 0.160
578
P FNC004 Fanconi Syndrome 60 0.160
579
c ACT073 Acute Leukemia 59 0.160
580
QDR001 Quadriplegia 49 0.160
581
MST005 Mastitis 52 0.160
582
PCD001 Pica Disease 38 0.160
583
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.160
584
P DMN002 Dementia 65 0.160
585
SPR006 Sparganosis 35 0.160
586
VRC001 Varicocele 48 0.160
587
P INT070 Intestinal Obstruction 57 0.160
588
P RTN018 Retinal Disease 53 0.160
589
P CWD010 Cowden Syndrome 70 0.160
590
GST040 Gastric Adenocarcinoma 66 0.160
591
BRN024 Bronchitis 67 0.160
592
BRR002 Barrett's Adenocarcinoma 37 0.160
593
SKN019 Skin Melanoma 70 0.160
594
P ZLL001 Zellweger Syndrome 65 0.160
595
ACT058 Active Peptic Ulcer Disease 55 0.160
596
PPT005 Peptic Ulcer Disease 58 0.160
597
P PLL002 Pellagra 46 0.160
598
OST012 Osteoarthritis 77 0.160
599
CYT002 Cytokine Deficiency 43 0.160
600
SYS003 Systolic Heart Failure 49 0.160
601
GRN017 Granulocytopenia 42 0.160
602
PLY100 Polyploidy 36 0.160
603
ETH012 Ethylene Glycol Poisoning 29 0.160
604
SPN186 Spinal Cord Injury 60 0.160
605
MSC193 Muscular Lipidosis 23 0.160
606
c ACQ047 Acquired Methemoglobinemia 30 0.160
607
ACT119 Acute Promyelocytic Leukemia 62 0.130
608
ALL003 Allergic Rhinitis 66 0.130
609
P ATR011 Atrial Fibrillation 66 0.130
610
CRB137 Cerebral Creatine Deficiency Syndrome 31 0.130
611
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 0.130
612
P MYP105 Myopathy, Myosin Storage, Autosomal Dominant 39 0.130
613
P PRG013 Paraganglioma 57 0.130
614
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.130
615
ING001 Inguinal Hernia 59 0.130
616
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 69 0.130
617
PHS025 Phosphatase, Acid, of Tissues 28 0.130
618
P MDL005 Medulloblastoma 75 0.130
619
c SCH079 Schizophrenia 1 44 0.130
620
KRT071 Keratosis, Seborrheic 56 0.130
621
c SML038 Small Cell Cancer of the Lung 68 0.130
622
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.130
623
CRZ001 Crouzon Syndrome 64 0.130
624
CRD223 Cardiac Arrhythmia 63 0.130
625
3HY007 3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency 51 0.130
626
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.130
627
CHR696 Charcot-Marie-Tooth Disease, X-Linked Recessive, 4, with or Without Cerebellar Ataxia 32 0.130
628
RFS006 Refsum Disease, Classic 63 0.130
629
P MCR129 Microvascular Complications of Diabetes 1 67 0.130
630
c CTR132 Cataract 3, Multiple Types 41 0.130
631
RGD003 Rigid Spine Muscular Dystrophy 1 56 0.130
632
PTR032 Peters-Plus Syndrome 63 0.130
633
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 59 0.130
634
P NSP012 Nasopharyngeal Carcinoma 60 0.130
635
MTC155 Mitochondrial Complex I Deficiency, Nuclear Type 7 24 0.130
636
CHR100 Chronic Ulcer of Skin 57 0.130
637
P FML011 Familial Adenomatous Polyposis 70 0.130
638
VTM002 Vitamin B12 Deficiency 48 0.130
639
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.130
640
EWN003 Ewing Sarcoma 69 0.130
641
c MTH083 Methemoglobinemia, Beta Type 21 0.130
642
c MTH084 Methemoglobinemia, Alpha Type 10 0.130
643
NRN005 Neuronal Ceroid-Lipofuscinoses 61 0.130
644
c MCR112 Microvascular Complications of Diabetes 2 42 0.130
645
PYR012 Pyruvate Dehydrogenase E1-Beta Deficiency 40 0.130
646
ANR007 Anorexia Nervosa 59 0.130
647
c DVL110 Developmental and Epileptic Encephalopathy 88 21 0.130
649
SLF014 Sulfite Oxidase Deficiency, Isolated 53 0.130
650
c SPS222 Spastic Paraplegia 20, Autosomal Recessive 56 0.130
651
P ALB003 Albinism-Deafness Syndrome 33 0.130
652
CMB017 Combined Oxidative Phosphorylation Deficiency 6 41 0.130
653
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.130
654
c TBR025 Tuberous Sclerosis 1 84 0.130
655
P HYP750 Hypertriglyceridemia, Familial 61 0.130
656
CNT105 Central Core Disease of Muscle 59 0.130
657
P TRT019 Torticollis 47 0.130
658
c HYP597 Hyperprolinemia, Type Ii 43 0.130
659
P MYS003 Myasthenia Gravis 67 0.130
660
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.130
661
TBL029 Tubulin, Beta 28 0.130
662
CRB150 Cerebral Creatine Deficiency Syndrome 2 54 0.130
663
P MYC007 Myocardial Infarction 69 0.130
664
P MJR001 Major Depressive Disorder 68 0.130
665
c LKM063 Leukemia, Chronic Myeloid 70 0.130
666
c CHR489 Charcot-Marie-Tooth Disease, Axonal, Type 2q 32 0.130
667
MLD001 Melioidosis 67 0.130
668
c BTT014 Beta-Thalassemia 72 0.130
669
HMF006 Hemifacial Microsomia 55 0.130
670
P HYP726 Hypercalcemia, Infantile, 1 58 0.130
671
CRT072 Creutzfeldt-Jakob Disease 67 0.130
672
MLT157 Multiple System Atrophy 1 69 0.130
673
P TRC072 Treacher Collins Syndrome 1 62 0.130
674
END057 Endometrial Cancer 76 0.130
675
PRK088 Parkinson Disease, Mitochondrial 19 0.130
676
CRD231 Cardiomyopathy, Infantile Histiocytoid 47 0.130
677
c BRS111 Breast-Ovarian Cancer, Familial 2 53 0.130
678
EPD015 Epidemic Typhus 44 0.130
679
P FTL001 Fetal Alcohol Syndrome 55 0.130
680
FBR009 Fibrous Dysplasia 48 0.130
681
P FML068 Familial Hypocalciuric Hypercalcemia 55 0.130
682
BCT021 Bacterial Sepsis 43 0.130
683
P HRD144 Hereditary Mixed Polyposis Syndrome 54 0.130
684
CMB007 Combined Immunodeficiency 56 0.130
685
P VNS003 Venous Insufficiency 54 0.130
686
OST003 Osteonecrosis 60 0.130
687
P MTC010 Mitochondrial Dna Depletion Syndrome 46 0.130
688
VTM033 Vitamin K Deficiency Bleeding 49 0.130
689
P PLY014 Polycystic Kidney Disease 71 0.130
690
P HYP111 Hyperprolinemia 44 0.130
691
CHR431 Chronic Venous Insufficiency 48 0.130
692
ANT018 Anthracosis 50 0.130
693
P MGR003 Migraine with Aura 51 0.130
694
PNC001 Pancytopenia 52 0.130
695
NRX001 Neuroaxonal Dystrophy 38 0.130
696
PST028 Post-Traumatic Stress Disorder 58 0.130
697
P CRN037 Craniosynostosis 67 0.130
698
c ATM011 Autoimmune Hepatitis 62 0.130
699
HYP080 Hypogonadism 49 0.130
700
P TMP001 Temporal Lobe Epilepsy 49 0.130
701
P LNG028 Long Qt Syndrome 63 0.130
702
MLG067 Malignant Giant Cell Tumor 28 0.130
703
P TBR001 Tuberous Sclerosis 69 0.130
704
OPS001 Opisthorchiasis 41 0.130
705
c CHR697 Charcot-Marie-Tooth Disease X-Linked Recessive 4 33 0.130
706
P NRD007 Neurodegeneration with Brain Iron Accumulation 51 0.130
707
URT010 Ureteral Obstruction 44 0.130
708
PSD009 Pseudohermaphroditism 46 0.130
709
TNC002 Tinea Capitis 42 0.130
710
NTR005 Nutritional Deficiency Disease 60 0.130
711
P EMB005 Embryonal Rhabdomyosarcoma 53 0.130
712
NPH009 Nephrolithiasis 54 0.130
713
P MTR014 Motor Neuron Disease 65 0.130
714
AMN001 Amenorrhea 53 0.130
715
RYS001 Reye Syndrome 49 0.130
716
P EPL164 Epilepsy 70 0.130
717
c VRL010 Viral Hepatitis 52 0.130
718
HMP005 Hemiplegia 53 0.130
719
MYS004 Myiasis 38 0.130
720
CRT012 Cortical Blindness 42 0.130
721
LCH001 Leech Infestation 37 0.130
722
KLB003 Klebsiella Pneumonia 49 0.130
723
P END044 Endometriosis 62 0.130
724
PYD002 Pyoderma 49 0.130
725
INT066 Interstitial Lung Disease 60 0.130
726
LYS002 Lysosomal Storage Disease 51 0.130
727
P TRT010 Teratoma 50 0.130
728
P PSD003 Pseudohypoaldosteronism 45 0.130
729
P HLP001 Holoprosencephaly 68 0.130
730
GTR002 Goiter 52 0.130
731
DBT002 Diabetic Autonomic Neuropathy 40 0.130
732
OST011 Osteomalacia 52 0.130
733
MCR013 Microphthalmia 59 0.130
734
LPR001 Lepromatous Leprosy 49 0.130
735
LMY002 Leiomyoma 51 0.130
736
P MGR001 Migraine Without Aura 48 0.130
737
MNT002 Mental Depression 56 0.130
738
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.130
739
DMP001 Dumping Syndrome 43 0.130
740
ALC010 Alcoholic Cardiomyopathy 42 0.130
741
CRY005 Cryptococcosis 61 0.130
742
DNG003 Dengue Disease 65 0.130
743
FLR001 Filarial Elephantiasis 59 0.130
744
GT001 Gout 63 0.130
745
P ART022 Arthritis 70 0.130
746
P SLP005 Sleep Disorder 61 0.130
747
MLG077 Malignant Peripheral Nerve Sheath Tumor 53 0.130
748
c INH020 Inherited Metabolic Disorder 47 0.130
749
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.130
750
BRS051 Breast Disease 58 0.130
751
ACQ007 Acquired Immunodeficiency Syndrome 58 0.130
752
INV005 Inverted Follicular Keratosis 31 0.130
753
P AXN001 Axonal Neuropathy 33 0.130
754
ILS001 Ileus 49 0.130
755
P NRF002 Neurofibromatosis 60 0.130
756
BLT006 Bilateral Breast Cancer 48 0.130
757
CRT055 Creatine Deficiency Syndromes 38 0.130
758
SCT002 Scotoma 42 0.130
759
BBS001 Babesiosis 48 0.130
760
DRM011 Dermatophytosis 52 0.130
761
P SDR003 Sideroblastic Anemia 49 0.130
762
P INF038 Influenza 68 0.130
763
GST039 Gastroduodenitis 37 0.130
764
INT007 Intermediate Coronary Syndrome 53 0.130
765
EMR021 Emery-Dreifuss Syndrome 11 0.130
766
TTR005 Tetrahydrobiopterin Deficiency 49 0.130
767
P THY032 Thyroiditis 56 0.130
768
CCN002 Cocaine Abuse 49 0.130
769
P RDC010 Reducing Body Myopathy 33 0.130
770
HYD005 Hydrocele 46 0.130
771
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.130
772
OVR094 Ovarian Epithelial Cancer 39 0.130
773
DST006 Diastolic Heart Failure 45 0.130
774
CNG506 Congenital Amyoplasia 27 0.130
775
GLM044 Glomerular Disease 34 0.130
776
MYT011 Myotonia 37 0.130
777
DPR016 Depression 64 0.130
778
P CRB088 Cerebral Atrophy 32 0.130
779
GLY085 Glycogen Storage Disease Due to Lactate Dehydrogenase Deficiency 16 0.130
780
MTH047 Methanol Poisoning 37 0.130
781
GRN033 Granulomatous Mastitis 31 0.130
782
CRD137 Cardiogenic Shock 56 0.130
783
ADT001 Auditory Agnosia 25 0.092
784
c 3MT007 3-Methylglutaconic Aciduria 37 0.092
785
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.092
786
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.092
787
MYP099 Myopathy, Isolated Mitochondrial, Autosomal Dominant 27 0.092
788
c MYP118 Myopathy, Myofibrillar, 8 31 0.092
789
MTC158 Mitochondrial Complex I Deficiency, Nuclear Type 10 26 0.092
790
MTC164 Mitochondrial Complex I Deficiency, Nuclear Type 17 24 0.092
791
SRB001 Sorbitol Dehydrogenase Deficiency with Peripheral Neuropathy 21 0.092
792
c FNC066 Fanconi Renotubular Syndrome 5 25 0.092
793
c AMY088 Amyotrophic Lateral Sclerosis 3 33 0.092
794
KFR001 Kufor-Rakeb Syndrome 59 0.092
795
SNS008 Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis 59 0.092
796
CRT007 Cortical Deafness 26 0.092
797
MYL009 Myelodysplastic Syndrome 67 0.092
798
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.092
799
c MLT068 Multiple Mitochondrial Dysfunctions Syndrome 1 45 0.092
800
LTN004 Late-Onset Retinal Degeneration 59 0.092
801
ASC010 Ascaris Lumbricoides Infection 49 0.092
802
P LYM118 Lymphoma 66 0.092
803
ART110 Arteritic Anterior Ischemic Optic Neuropathy 34 0.092
804
TNG009 Tongue Squamous Cell Carcinoma 43 0.092
805
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.092
806
PNG002 Pain Agnosia 51 0.092
807
P HRD021 Hereditary Sensory Neuropathy 48 0.092
808
c PRT132 Protoporphyria, Erythropoietic, 1 61 0.092
809
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 63 0.092
810
LPD012 Lipoid Congenital Adrenal Hyperplasia 68 0.092
811
CYS019 Cystathioninuria 46 0.092
812
c NTR047 Neutropenia, Severe Congenital, 1, Autosomal Dominant 37 0.092
813
ALK013 Alkaptonuria 58 0.092
814
c MTC056 Mitochondrial Dna Depletion Syndrome 4a 62 0.092
815
CYS044 Cystic Disease of Lung 19 0.092
816
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 68 0.092
817
P OST002 Osteoporosis 76 0.092
818
CRN048 Craniofacial-Deafness-Hand Syndrome 52 0.092
819
c DNT027 Dentin Dysplasia, Type Ii 36 0.092
820
P MJR007 Major Affective Disorder 1 42 0.092
821
EXF001 Exfoliation Syndrome 55 0.092
822
c SCL052 Scleroderma, Familial Progressive 60 0.092
823
P PLV020 Pelvic Organ Prolapse 57 0.092
824
PLM061 Pulmonary Edema of Mountaineers 25 0.092
825
c RTN150 Retinitis Pigmentosa 10 44 0.092
826
LYM133 Lymphoma, Hodgkin, Classic 69 0.092
827
MTC207 Mitochondrial Complex Ii Deficiency, Nuclear Type 1 57 0.092
828
c MCL013 Mucolipidosis Iv 64 0.092
829
CRN295 Carnitine Palmitoyltransferase I Deficiency 55 0.092
830
MYP097 Myopathy with Lactic Acidosis, Hereditary 33 0.092
831
MYP091 Myopathy, Congenital, with Fiber-Type Disproportion 44 0.092
832
c NPH055 Nephrotic Syndrome, Type 1 52 0.092
833
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 0.092
834
c GLC092 Glaucoma, Primary Open Angle 60 0.092
835
CRD132 Cardiac Conduction Defect 59 0.092
836
P HYP768 Hyperlipoproteinemia, Type I 67 0.092
837
HYP784 Hypogonadism, Male 43 0.092
838
MTH076 Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency 50 0.092
839
MYC079 Myoclonic Epilepsy of Lafora 63 0.092
840
MYC080 Myoclonic Epilepsy of Unverricht and Lundborg 52 0.092
841
SPN354 Spinal Arachnoiditis 35 0.092
842
c SYN084 Synpolydactyly 1 36 0.092
843
c GLC112 Galactosemia Iii 51 0.092
844
c GLY008 Glycogen Storage Disease Ii 72 0.092
845
PYR022 Pyruvate Dehydrogenase E1-Alpha Deficiency 63 0.092
846
c SPN225 Spondyloarthropathy 1 70 0.092
847
c PRD040 Periodontitis, Chronic 52 0.092
848
GTL001 Gitelman Syndrome 65 0.092
849
ENC055 Encephalopathy, Ethylmalonic 51 0.092
850
c TTH011 Tooth Agenesis, Selective, 2 13 0.092
851
SPP011 Suppression of Tumorigenicity 12 61 0.092
852
c DFN251 Deafness, Autosomal Dominant 11 44 0.092
853
c LNG048 Long Qt Syndrome 3 52 0.092
854
SCT005 Scott Syndrome 51 0.092
855
DNN001 Danon Disease 59 0.092
856
GRN051 Granulomatous Disease, Chronic, X-Linked 57 0.092
857
CNG184 Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects 56 0.092
858
MTC149 Mitochondrial Complex I Deficiency, Mitochondrial Type 1 14 0.092
859
P D2H002 D-2-Hydroxyglutaric Aciduria 1 53 0.092
860
c ART068 Aortic Aneurysm, Familial Thoracic 2 34 0.092
861
EPL050 Epilepsy, Partial, with Pericentral Spikes 26 0.092
862
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 58 0.092
863
ART164 Arthrogryposis Multiplex Congenita 1, Neurogenic, with Myelin Defect 24 0.092
864
MTC156 Mitochondrial Complex I Deficiency, Nuclear Type 8 21 0.092
865
ART166 Arthrogryposis Multiplex Congenita 4, Neurogenic, with Agenesis of the Corpus Callosum 22 0.092
866
HYP017 Hypophosphatemia 49 0.092
867
CRR001 Carrion's Disease 31 0.092
868
HYP025 Hyperphosphatemia 47 0.092
869
c PRM032 Primary Congenital Glaucoma 40 0.092
870
TNS007 Taeniasis 46 0.092
871
INT017 Intestinal Schistosomiasis 51 0.092
872
CNN008 Cinnamon Odor, Pleasantness of 13 0.092
873
c MCR312 Microphthalmia, Syndromic 10 39 0.092
874
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.092
875
c LNG047 Long Qt Syndrome 2 59 0.092
876
HRT037 Heart and Brain Malformation Syndrome 32 0.092
877
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 0.092
878
ART167 Arthrogryposis Multiplex Congenita 5 21 0.092
879
c SPR162 Spermatogenic Failure 50 42 0.092
880
IMM065 Immunodeficiency 10 47 0.092
881
DSR012 Disordered Steroidogenesis Due to Cytochrome P450 Oxidoreductase Deficiency 39 0.092
882
P HMG032 Hemoglobin H Disease 51 0.092
883
AKL001 Au-Kline Syndrome 38 0.092
884
c DFN360 Deafness, Autosomal Dominant 69 34 0.092
885
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 0.092
886
ADR016 Adrenal Cortical Carcinoma 61 0.092
887
P LSS002 Lissencephaly 52 0.092
888
PLY001 Polycythemia Vera 69 0.092
889
P DNT020 Dent Disease 1 63 0.092
890
MSC152 Muscular Dystrophy, Becker Type 69 0.092
891
LWC002 Lowe Oculocerebrorenal Syndrome 68 0.092
892
WLF001 Wolff-Parkinson-White Syndrome 63 0.092
893
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.092
894
ARG007 Argininemia 58 0.092
895
c PRX059 Peroxisome Biogenesis Disorder 1a 57 0.092
896
ENT011 Enterocolitis 55 0.092
897
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.092
898
KRT019 Keratitis, Hereditary 66 0.092
899
P KBK002 Kabuki Syndrome 1 66 0.092
900
CTY001 Cat Eye Syndrome 45 0.092
901
KPS004 Kaposi Sarcoma 76 0.092
902
SYR010 Syringomyelia, Noncommunicating Isolated 36 0.092
903
P TTR001 Tetralogy of Fallot 69 0.092
904
TRG002 Trigeminal Neuralgia 61 0.092
905
PCK003 Pick Disease of Brain 70 0.092
906
GRG001 Greig Cephalopolysyndactyly Syndrome 64 0.092
907
PRP083 Porphyria, Acute Intermittent 64 0.092
908
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.092
909
HRD029 Hereditary Leiomyomatosis and Renal Cell Cancer 56 0.092
910
P HYP058 Hypervitaminosis a 47 0.092
911
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 63 0.092
912
HLT002 Halothane Hepatitis 32 0.092
913
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.092
914
MLL018 Miller-Dieker Lissencephaly Syndrome 53 0.092
915
MYL013 Myeloperoxidase Deficiency 44 0.092
916
c GRV008 Graves Disease 1 54 0.092
917
MTC147 Mitochondrial Complex I Deficiency, Nuclear Type 12 21 0.092
918
FBR012 Fabry Disease 71 0.092
919
STR081 Stormorken Syndrome 56 0.092
920
P STR020 Strabismus 56 0.092
921
c THR092 Thrombophilia Due to Thrombin Defect 74 0.092
923
c RTN143 Retinitis Pigmentosa 47 42 0.092
924
c LBR006 Leber Congenital Amaurosis 11 35 0.092
925
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.092
926
CNZ006 Coenzyme Q10 Deficiency, Primary, 1 42 0.092
927
c ART101 Aortic Valve Disease 2 65 0.092
928
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.092
929
LGN006 Legionnaire Disease 52 0.092
930
c MYC058 Myocardial Infarction 2 23 0.092
931
c ATS371 Autism 6 21 0.092
932
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.092
933
INT258 Interstitial Nephritis, Karyomegalic 46 0.092
934
c INC015 Inclusion Body Myopathy with Early-Onset Paget Disease with or Without Frontotemporal Dementia 2 33 0.092
935
P TMR010 Tumor Predisposition Syndrome 69 0.092
936
c PRS114 Prostate Cancer, Hereditary, 2 33 0.092
937
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 50 0.092
938
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 52 0.092
939
HYP555 Hypertriglyceridemia, Transient Infantile 39 0.092
940
c RTN140 Retinitis Pigmentosa 67 32 0.092
941
HRN029 Hearing Loss, Noise-Induced 37 0.092
942
HRS016 Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction 26 0.092
943
P MGL010 Megalencephalic Leukoencephalopathy with Subcortical Cysts 2a 39 0.092
944
APN008 Apnea, Obstructive Sleep 66 0.092
945
P LKM071 Leukemia, Chronic Lymphocytic 74 0.092
946
THY111 Thyroid Carcinoma, Familial Medullary 67 0.092
947
c