Search results for NADH

1225 hits were found for NADH

# Family MCID Name MIFTS Score
1
MTH026 Methemoglobinemia Due to Deficiency of Methemoglobin Reductase 35 44.624
2
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 61 41.306
3
P MTH007 Methemoglobinemia 46 10.669
4
P MPL001 Maple Syrup Urine Disease 70 10.018
5
PYR031 Pyruvate Dehydrogenase E3-Binding Protein Deficiency 43 9.193
6
DHY010 Dihydrolipoamide Dehydrogenase Deficiency 47 9.193
7
ANX004 Anoxia 40 9.107
8
c CNG223 Congenital Methemoglobinemia 39 9.019
9
P MYP004 Myopathy 67 7.725
10
P LCT001 Lactic Acidosis 51 6.566
11
HYP266 Hypoxia 57 6.490
12
MTC005 Mitochondrial Metabolism Disease 45 6.409
13
P OPT006 Optic Nerve Disease 58 6.115
14
P MTC133 Mitochondrial Myopathy 50 6.080
15
P HRD217 Hereditary Optic Neuropathy 36 6.041
16
P NRP001 Neuropathy 60 5.193
17
P MTC069 Mitochondrial Disorders 57 5.133
18
CYN002 Cyanosis, Transient Neonatal 43 5.128
19
FTT001 Fatty Liver Disease 62 5.036
20
LBR038 Leber Hereditary Optic Neuropathy, Modifier of 62 4.935
21
P MYC084 Mycobacterium Tuberculosis 1 68 4.843
22
HLX001 Helix Syndrome 48 4.715
23
P PRK039 Parkinsonism 55 4.638
24
HYP066 Hyperglycemia 61 4.603
25
P NRB001 Neuroblastoma 66 4.383
26
c ATS307 Autosomal Recessive Cerebellar Ataxia 39 4.211
27
LGH007 Leigh Syndrome 70 4.202
28
P ENC018 Encephalopathy 62 3.978
29
MTC004 Mitochondrial Encephalomyopathy 42 3.966
30
CHR066 Chronic Fatigue Syndrome 60 3.873
31
GLL048 Glial Tumor 52 3.855
32
GLM045 Glioma 63 3.855
33
NNL005 Non-Alcoholic Fatty Liver Disease 63 3.843
34
CHG001 Chagas Disease 66 3.801
35
P ALZ034 Alzheimer Disease 87 3.781
36
c ATR087 Atrial Standstill 1 74 3.559
37
AGN016 Aging 54 3.540
38
HYP056 Hypoglycemia 65 3.461
39
ECH003 Echinococcosis 53 3.428
40
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 3.374
41
CHL014 Cholera 62 3.319
42
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 62 3.287
43
LPD008 Lipid Metabolism Disorder 62 3.287
44
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 3.227
45
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 44 3.189
46
BRN071 Brain Injury 50 3.088
47
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 3.079
48
PRT037 Pertussis 65 3.066
49
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 3.043
50
P HYP265 Hypotonia 42 3.043
51
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 2.998
52
P BRS047 Breast Cancer 98 2.959
53
c MCR115 Microvascular Complications of Diabetes 5 65 2.922
54
CYS001 Cystic Fibrosis 78 2.899
55
P CHR012 Chronic Granulomatous Disease 69 2.890
56
MTB004 Metabolic Acidosis 48 2.885
57
P KLZ004 Kala-Azar 1 41 2.857
58
LSH001 Leishmaniasis 64 2.857
59
IRN002 Iron Metabolism Disease 57 2.857
60
48X005 48,xyyy 39 2.827
61
P MSC005 Muscular Dystrophy 67 2.797
62
47X002 47,xyy 48 2.793
63
P DYS154 Dystonia 64 2.786
64
HMP009 Haemophilus Influenzae 41 2.786
65
CTR172 Citrullinemia, Classic 65 2.736
66
CRT015 Carotid Artery Occlusion 45 2.705
67
P PRK057 Parkinson Disease, Late-Onset 80 2.691
68
OST159 Osteogenic Sarcoma 66 2.691
69
P HNT016 Huntington Disease 73 2.656
70
CRB004 Cerebral Artery Occlusion 45 2.642
71
ISC004 Ischemia 61 2.635
72
MTH072 Methemoglobin Reductase Deficiency 15 2.597
73
c MJR022 Major Affective Disorder 8 38 2.595
74
c MJR024 Major Affective Disorder 9 41 2.595
75
P BPL003 Bipolar Disorder 56 2.595
76
TRM010 Traumatic Brain Injury 51 2.584
77
P HYP061 Hypertrophic Cardiomyopathy 69 2.566
78
LBR036 Leber Plus Disease 66 2.546
79
GLB002 Glioblastoma 67 2.546
80
ALC007 Alcohol Dependence 66 2.509
81
c DLT002 Dilated Cardiomyopathy 78 2.440
82
P GST053 Gastric Cancer 83 2.425
83
CYS008 Cystic Echinococcosis 57 2.420
84
P MSC003 Muscular Atrophy 52 2.404
85
P SZR006 Seizure Disorder 70 2.389
86
MLR004 Malaria 80 2.389
87
RNL114 Renal Cell Carcinoma, Nonpapillary 80 2.389
88
HRW001 Hair Whorl 35 2.389
89
DYS015 Dysentery 50 2.381
90
NRM005 Neuromuscular Disease 63 2.367
91
PST092 Posttransplant Acute Limbic Encephalitis 28 2.347
92
P CTR177 Citrullinemia, Type Ii, Adult-Onset 55 2.334
93
ART140 Arteries, Anomalies of 53 2.334
94
LPP008 Lipoprotein Quantitative Trait Locus 65 2.334
95
SCC003 Succinic Acidemia 10 2.308
96
ATH013 Atherosclerosis Susceptibility 63 2.304
97
KRN002 Kearns-Sayre Syndrome 63 2.292
98
CRN030 Coronary Stenosis 50 2.285
99
c BRN108 Branchiootic Syndrome 1 62 2.260
100
DNT012 Dental Caries 53 2.260
101
c AMY091 Amyotrophic Lateral Sclerosis 1 88 2.253
102
P LTR001 Lateral Sclerosis 58 2.253
103
HYP060 Hyperinsulinism 54 2.253
104
CHL068 Cholestasis 61 2.244
105
ATS010 Autosomal Recessive Disease 42 2.235
106
P SPP010 Suppressor of Tumorigenicity 3 51 2.215
107
P CTR002 Cataract 60 2.215
108
STN013 Stenotrophomonas Maltophilia Infection 26 2.213
109
c HPT001 Hepatitis C 62 2.213
110
P MLN008 Melanoma 76 2.183
111
P PHC003 Pheochromocytoma 69 2.172
112
CNG393 Congenital Muscular Dystrophy with Hyperlaxity 12 2.172
113
c HPT073 Hepatitis C Virus 71 2.131
114
SLP001 Sleeping Sickness 56 2.119
115
P VSC007 Vascular Disease 63 2.119
116
ALL014 Allergic Encephalomyelitis 34 2.119
117
c HYP836 Hypercholesterolemia, Familial, 1 73 2.088
118
ORL011 Oral Cancer 60 2.088
119
P RSP003 Respiratory Failure 74 2.069
120
P LVR013 Liver Disease 69 2.054
121
SQM006 Squamous Cell Carcinoma 60 2.044
122
P BRS044 Breast Adenocarcinoma 58 2.017
123
GLC003 Glucose Intolerance 54 1.998
124
CRB090 Cerebral Hypoxia 42 1.998
125
c DNT047 Dentinogenesis Imperfecta Type 2 35 1.998
126
P ATS364 Autism 69 1.951
127
c HYP595 Hypertension, Essential 85 1.951
128
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 17 1.951
129
PRM329 Premature Aging 36 1.905
130
P INF032 Infertility 57 1.905
131
P LPR021 Leprosy 3 71 1.903
132
URT049 Urate Oxidase, Pseudogene 24 1.903
133
P MCR010 Microcephaly 60 1.903
134
HNS001 Hansen's Disease 32 1.903
135
CND006 Candida Glabrata 30 1.903
136
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 1.853
137
RPD005 Rapidly Involuting Congenital Hemangioma 46 1.853
138
HYP014 Hyperuricemia 51 1.853
139
CNT047 Contact Dermatitis 57 1.846
140
c MCR130 Microvascular Complications of Diabetes 6 41 1.845
141
c MCR120 Microvascular Complications of Diabetes 7 47 1.845
142
c MCR113 Microvascular Complications of Diabetes 3 52 1.845
143
c MCR133 Microvascular Complications of Diabetes 4 41 1.845
144
P SCK005 Sickle Cell Disease 56 1.845
145
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.800
146
HMC014 Homocysteinemia 52 1.800
147
P SCH015 Schizophrenia 74 1.800
148
P PRS040 Prostate Cancer 95 1.800
149
c CHR095 Chronic Progressive External Ophthalmoplegia 49 1.800
150
P LPS004 Lupus Erythematosus 61 1.800
151
P MYC033 Myoclonus 47 1.800
152
c THY056 Thyroid Dyshormonogenesis 3 31 1.782
153
CHL065 Cholangiocarcinoma 58 1.782
154
TRN015 Transient Cerebral Ischemia 63 1.782
155
INT079 Intrahepatic Cholangiocarcinoma 51 1.782
156
P PLM037 Pulmonary Hypertension 72 1.770
157
DBT010 Diabetic Neuropathy 54 1.770
158
P THL005 Thalassemia 56 1.746
159
CRV035 Cervical Cancer 73 1.746
160
c SYS001 Systemic Lupus Erythematosus 87 1.746
161
P MLT020 Multiple Sclerosis 79 1.746
162
P FBR017 Fibrosarcoma 56 1.746
163
HDN002 Head Injury 44 1.746
164
CRV040 Cervix Carcinoma 50 1.715
165
PPL052 Papillomatosis, Confluent and Reticulated 34 1.691
166
ART002 Arts Syndrome 66 1.689
167
P PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 54 1.689
168
P ANP001 Anaplastic Large Cell Lymphoma 61 1.689
169
c LKM061 Leukemia, Acute Myeloid 83 1.689
170
c ACT068 Acute Cystitis 61 1.689
171
TTN003 Tetanus 65 1.689
172
P PTS002 Ptosis 52 1.689
173
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.650
174
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.650
175
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.650
176
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 1.650
177
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 1.650
178
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.650
179
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 1.650
180
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.650
181
c TYP009 Type 2 Diabetes Mellitus 92 1.650
182
P PRD008 Periodontitis 64 1.650
183
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 1.650
184
TXC005 Toxic Shock Syndrome 62 1.650
185
STT001 Status Epilepticus 59 1.650
186
SPS057 Spasticity 42 1.629
187
VLV047 Volvulus of Midgut 52 1.629
188
P EXN002 Exanthem 58 1.629
189
SCK003 Sickle Cell Anemia 74 1.629
190
c PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 49 1.629
191
OCL069 Ocular Motor Apraxia 57 1.629
192
c PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 53 1.629
193
c HYP807 Hyperinsulinemic Hypoglycemia, Familial, 6 52 1.629
194
ORL015 Oral Squamous Cell Carcinoma 43 1.629
195
P CRD119 Cardiac Arrest 67 1.629
196
P MYC008 Myocarditis 59 1.629
197
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 41 1.608
198
P LNG032 Lung Cancer 98 1.566
199
P BLD134 Bladder Cancer 79 1.566
200
ACT098 Acute Erythroid Leukemia 55 1.566
201
P FRD001 Friedreich Ataxia 61 1.566
202
DBT084 Diabetes Mellitus, Ketosis-Prone 60 1.566
203
P MLG056 Malignant Hyperthermia 66 1.566
204
P CRV031 Cervical Adenocarcinoma 48 1.566
205
INS001 Insulinoma 59 1.566
206
P GST044 Gastritis 55 1.566
207
INT071 Intestinal Perforation 49 1.566
208
ALV002 Alveolar Echinococcosis 57 1.566
209
P HPT021 Hepatitis 69 1.566
210
FLR002 Filariasis 55 1.566
211
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 1.566
212
PHN003 Phenylketonuria 76 1.566
213
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.564
214
P PSR002 Psoriasis 63 1.564
215
PST011 Pustulosis of Palm and Sole 52 1.564
216
GRD001 Giardiasis 46 1.564
217
CRB037 Cerebral Palsy 67 1.564
218
ADR040 Adrenal Gland Pheochromocytoma 46 1.521
220
P BCL017 B-Cell Lymphoma 59 1.521
221
P SKN015 Skin Carcinoma 71 1.521
222
c ACT071 Acute Kidney Failure 60 1.521
223
c MGR028 Migraine with or Without Aura 1 64 1.499
224
OTT002 Otitis Media 71 1.499
225
P MYL006 Myeloid Leukemia 61 1.499
226
c PRC016 Pre-Eclampsia 65 1.499
227
HGH043 High Grade Glioma 45 1.499
228
LTH004 Lathyrism 15 1.499
229
SVR001 Severe Acute Respiratory Syndrome 67 1.477
230
P GLC113 Galactosemia I 66 1.476
231
HPT022 Hepatoblastoma 54 1.476
232
CNG034 Congestive Heart Failure 69 1.476
233
P TRM003 Tremor 48 1.429
234
P LNG064 Lung Cancer Susceptibility 3 70 1.429
235
INS024 Insulin-Like Growth Factor I 78 1.426
236
VSC003 Visceral Leishmaniasis 55 1.426
237
RSC001 Rosacea 55 1.426
238
PRM236 Primary Biliary Cholangitis 60 1.426
239
ONC002 Onchocerciasis 51 1.426
240
PTH003 Pathologic Nystagmus 52 1.426
241
DYS073 Dysphagia 53 1.426
242
c RNG015 Ring Chromosome 2 22 1.426
243
P MYP087 Myopathy, Tubular Aggregate, 1 49 1.416
244
c TYP008 Type 1 Diabetes Mellitus 70 1.381
245
BRN004 Brain Edema 54 1.381
246
RBF001 Riboflavin Deficiency 49 1.378
247
LCT008 Lactate Dehydrogenase Deficiency 14 1.377
248
CYN003 Cyanide Poisoning 22 1.347
249
MSC007 Muscle Hypertrophy 64 1.347
250
INF034 Infective Endocarditis 54 1.347
251
c THY071 Thyroid Dyshormonogenesis 1 31 1.347
252
RTN212 Retinal Dystrophy with or Without Macular Staphyloma 31 1.347
253
P MTH008 Methylmalonic Acidemia 52 1.347
254
PRT036 Peritonitis 65 1.347
255
CLR030 Clear Cell Renal Cell Carcinoma 54 1.347
256
P CCK001 Cockayne Syndrome 68 1.347
257
P ECL001 Eclampsia 52 1.347
258
GLC009 Glucosephosphate Dehydrogenase Deficiency 53 1.347
259
CHL123 Chlamydia 58 1.347
260
P END033 Endocarditis 58 1.347
261
P BNG032 Benign Mesothelioma 53 1.347
262
P PRP029 Porphyria 60 1.347
263
ISL099 Isolated Methylmalonic Acidemia 36 1.347
264
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 1.330
265
DFC004 Deficiency Anemia 74 1.330
266
BCT022 Bacterial Infectious Disease 56 1.330
267
MTH071 Methane Production 25 1.278
268
P BRG001 Brugada Syndrome 69 1.278
269
ARG004 Argyria 26 1.278
270
CYS005 Cysticercosis 60 1.278
271
PRP027 Peripheral Vascular Disease 71 1.260
272
ANG054 Angina Pectoris 66 1.260
273
EXT007 Extracutaneous Mastocytoma 38 1.260
274
MST004 Mast Cell Neoplasm 42 1.260
275
P HRD018 Hair Disease 44 1.260
276
HLL004 Hellp Syndrome 53 1.260
277
KRT002 Keratomalacia 55 1.240
278
c SPR086 Spermatogenic Failure 3 46 1.224
279
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 1.224
280
P PNC035 Pancreatic Cancer 86 1.224
281
P HML002 Hemolytic Anemia 62 1.224
282
P RRH023 Rare Hereditary Hemochromatosis 54 1.224
283
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 1.224
284
HMS001 Hemosiderosis 48 1.224
285
SCH014 Schistosomiasis 56 1.224
286
P HYP076 Hyperthyroidism 53 1.224
287
HRT015 Heritable Pulmonary Arterial Hypertension 46 1.224
288
BRN056 Bronchopulmonary Dysplasia 56 1.224
289
CRT020 Cortisone Reductase Deficiency 34 1.209
290
c PLM164 Pulmonary Hypertension, Primary, 1 76 1.167
291
P ALC033 Alcohol Use Disorder 61 1.167
292
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.167
293
P LKM002 Leukemia 67 1.167
294
c ACT027 Acute Pancreatitis 60 1.167
295
MNK001 Menkes Disease 64 1.161
296
BRK010 Burkitt Lymphoma 66 1.161
297
LBR031 Leber Optic Atrophy and Dystonia 39 1.161
298
DWN001 Down Syndrome 70 1.161
299
ESP021 Esophageal Cancer 83 1.161
300
ORG002 Organic Acidemia 44 1.161
301
PRX097 Paroxysmal Dystonia 32 1.161
302
LYD001 Leydig Cell Tumor 45 1.161
303
P HYD006 Hydrocephalus 61 1.161
304
CRB039 Cerebrovascular Disease 66 1.161
305
P LRY044 Larynx Cancer 54 1.161
306
c SPR009 Sporadic Breast Cancer 42 1.108
307
c THY107 Thymoma, Familial 42 1.107
308
ONC007 Oncocytoma 50 1.107
309
P OVR042 Ovarian Cancer 88 1.107
310
P CLR023 Colorectal Cancer 100 1.107
311
c DVL036 Developmental and Epileptic Encephalopathy 39 39 1.107
312
P HPT023 Hepatocellular Carcinoma 96 1.107
313
DSS032 Disease by Infectious Agent 55 1.107
314
HPT004 Hepatic Coma 43 1.107
315
c CHR684 Chronic Kidney Disease 69 1.107
316
P MLN007 Male Infertility 56 1.107
317
HPT019 Hepatic Encephalopathy 59 1.107
318
DPH001 Diphtheria 59 1.107
319
P HRT032 Heart Disease 81 1.107
320
P MYG005 Myoglobinuria 40 1.107
321
P PRP019 Peripheral Nervous System Disease 58 1.107
322
P THY023 Thymoma 64 1.107
323
LKS001 Leukostasis 41 1.107
324
P RRT020 Rare Tumor 39 1.044
325
P DFN349 Deafness, Nonsyndromic Sensorineural, Mitochondrial 34 1.044
326
KRT058 Keratoderma, Palmoplantar, with Deafness 43 1.044
327
HMM004 Hamamy Syndrome 39 1.044
328
SNG007 Sengers Syndrome 45 1.044
329
MYL069 Myeloma, Multiple 77 1.044
330
PLT031 Platelet Membrane Fluidity 28 1.044
331
SCR011 Scrapie 39 1.044
332
PRS034 Parasitic Helminthiasis Infectious Disease 51 1.044
333
ALL010 Allergic Contact Dermatitis 56 1.044
334
P BRN006 Branchiootorenal Syndrome 50 1.044
335
CNR001 Coenurosis 26 1.044
336
TNS005 Tonsillitis 57 1.044
337
P GRV001 Graves' Disease 55 1.044
338
ANS011 Anus Cancer 57 1.044
339
NNS010 Nonsyndromic Hearing Loss and Deafness, Mitochondrial 13 1.044
340
PRS119 Persistent Genital Arousal Disorder 18 1.044
341
P LKM062 Leukemia, Acute Lymphoblastic 69 1.044
342
BRT005 Barth Syndrome 56 1.044
343
RCH002 Richards-Rundle Syndrome 31 1.044
344
P SCL018 Scoliosis 57 1.044
345
THY029 Thyroid Carcinoma 51 1.044
346
P DBT009 Diabetes Mellitus 67 1.044
347
YLL002 Yellow Fever 61 1.044
348
PLC005 Placental Insufficiency 56 1.044
349
MLT006 Multidrug-Resistant Tuberculosis 47 1.044
350
ADN018 Adenoma 59 1.044
351
END086 End Stage Renal Disease 52 1.044
352
P BRB001 Beriberi 44 1.044
353
P ADN016 Adenocarcinoma 63 1.044
354
P INS002 in Situ Carcinoma 53 1.044
355
SPN186 Spinal Cord Injury 61 0.976
356
c ACT134 Acute Liver Failure 59 0.976
357
ACR009 Acromesomelic Dysplasia, Hunter-Thompson Type 41 0.976
358
P RTN008 Retinitis Pigmentosa 80 0.976
359
c OPT053 Optic Atrophy 1 62 0.976
360
c L2H001 L-2-Hydroxyglutaric Aciduria 49 0.976
361
P APL001 Aplastic Anemia 73 0.976
362
c 2HY001 2-Hydroxyglutaric Aciduria 38 0.976
364
BTT016 Batten-Turner Congenital Myopathy 53 0.976
365
c CHL116 Cholestasis, Intrahepatic, of Pregnancy, 1 52 0.976
366
NRR001 Neuroretinitis 42 0.976
367
MDD018 Middle East Respiratory Syndrome 44 0.976
368
RTN023 Retinitis 46 0.976
369
P MVM001 Movement Disease 61 0.976
370
P RNV001 Renovascular Hypertension 49 0.976
371
SKN016 Skin Disease 63 0.976
372
P CNT004 Centronuclear Myopathy 57 0.976
373
SPN035 Spindle Cell Sarcoma 54 0.976
374
P RTN016 Retinal Degeneration 52 0.976
376
P SNS001 Sensorineural Hearing Loss 59 0.976
377
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.976
378
P BRS053 Breast Fibroadenoma 49 0.976
379
P GLY013 Glycogen Storage Disease 60 0.976
380
SRC014 Sarcoma 65 0.976
381
LVR012 Liver Cirrhosis 63 0.976
382
P ADL010 Adult Respiratory Distress Syndrome 71 0.976
383
CYT002 Cytokine Deficiency 43 0.976
384
MSC157 Muscular Dystrophy, Duchenne Type 79 0.904
385
STR067 Stroke, Ischemic 80 0.904
386
P MYS005 Myositis 56 0.904
387
c PRM108 Primary Progressive Multiple Sclerosis 51 0.904
388
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.904
389
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.904
390
c PCH010 Pachyonychia Congenita 3 43 0.904
391
P ASP006 Aspergillosis 72 0.904
392
P GLM040 Glioma Susceptibility 1 71 0.904
393
RNL077 Renal Fibrosis 46 0.904
394
P PLY041 Polymyositis 59 0.904
395
INT075 Intracranial Hypertension 53 0.904
396
P RBL001 Rubella 58 0.904
397
VCC001 Vaccinia 47 0.904
398
TRY001 Trypanosomiasis 50 0.904
399
P DRM010 Dermatomyositis 61 0.904
400
RCK004 Rickets 68 0.904
401
TLN003 Telangiectasis 51 0.904
402
ALC006 Alcoholic Hepatitis 61 0.904
403
PSY004 Psychotic Disorder 66 0.904
404
CCC002 Coccidiosis 50 0.904
405
MLG169 Malignant Astrocytoma 57 0.904
406
ERL001 Early Myoclonic Encephalopathy 62 0.904
407
P KDN017 Kidney Cancer 61 0.904
408
GST045 Gastroenteritis 58 0.904
409
DBT007 Diabetic Cataract 36 0.904
410
IDP022 Idiopathic Spinal Cord Herniation 17 0.904
411
P DBT005 Diabetes Insipidus 54 0.891
412
P MCH002 Machado-Joseph Disease 62 0.891
413
ALZ029 Alzheimer Disease Mitochondrial 24 0.891
414
ARG002 Argininosuccinic Aciduria 61 0.891
415
ASP002 Aspartylglucosaminuria 58 0.891
416
SPS007 Spastic Cerebral Palsy 46 0.891
417
APR001 Apraxia 52 0.891
418
PNB004 Panbronchiolitis, Diffuse 34 0.891
419
HYP690 Hyper-Beta-Alaninemia 24 0.891
420
EST002 Estrogen-Receptor Negative Breast Cancer 45 0.891
421
P BLD062 Bile Duct Cancer 67 0.891
422
PTN001 Patent Foramen Ovale 62 0.891
423
P DRR001 Diarrhea 55 0.891
424
MYP161 Myopathy, Congenital Proximal, with Minicore Lesions 17 0.855
425
PRS129 Prostatic Hyperplasia, Benign 49 0.825
426
FRN006 Frontotemporal Dementia 68 0.825
427
PLY150 Polykaryocytosis Inducer 29 0.825
428
P ATX030 Ataxia-Telangiectasia 80 0.825
429
HMN044 Human Immunodeficiency Virus Type 1 78 0.825
430
c ATS007 Autism Spectrum Disorder 72 0.825
431
CLT003 Colitis 63 0.825
432
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.825
433
P MYC007 Myocardial Infarction 70 0.825
434
P HYP098 Hypereosinophilic Syndrome 66 0.825
435
P CND004 Candidiasis 58 0.825
436
P RNL017 Renal Oncocytoma 54 0.825
437
PRP016 Paraplegia 52 0.825
438
CHL045 Choline Deficiency Disease 39 0.825
439
STR103 Streptococcus Pneumonia 47 0.825
440
CRN019 Coronary Artery Vasospasm 47 0.825
441
CNS004 Constipation 56 0.825
442
PRS021 Prostatic Adenoma 43 0.825
443
c BSL007 Basal Cell Carcinoma 68 0.825
444
FCL014 Focal Epilepsy 53 0.825
445
P RNL015 Renal Hypertension 45 0.825
446
LYM017 Lyme Disease 62 0.825
447
PRS045 Prostatic Hypertrophy 53 0.825
448
SVR004 Severe Combined Immunodeficiency 72 0.825
449
P ART021 Arteriosclerosis 54 0.825
450
P OVR049 Ovarian Disease 52 0.825
451
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.825
452
STM007 Stomatitis 54 0.825
453
MYC005 Myocardial Stunning 46 0.825
454
WLL004 Wallerian Degeneration 38 0.825
455
P MRC003 Mercury Poisoning 49 0.825
456
P MYC026 Myoclonus Epilepsy 35 0.825
457
MYC015 Mycobacterium Fortuitum 28 0.825
458
ADR022 Adrenomyeloneuropathy 39 0.738
459
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 0.738
460
P CRN300 Coronary Heart Disease 1 73 0.738
461
ADR007 Adrenoleukodystrophy 73 0.738
462
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 50 0.738
463
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.738
464
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.738
465
ATM095 Autoimmune Disease 61 0.738
466
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 0.738
467
P SLP006 Sleep Apnea 69 0.738
468
FML037 Female Breast Cancer 51 0.738
469
CHK001 Chikungunya 60 0.738
470
P URN019 Urinary Tract Infection 49 0.738
471
NNL006 Non-Alcoholic Steatohepatitis 54 0.738
472
HLC007 Helicobacter Pylori Infection 67 0.738
473
VRC005 Varicose Veins 60 0.738
474
c HYP368 Hyperphenylalaninemia, Bh4-Deficient, C 37 0.738
475
MNN043 Meningioma, Familial 79 0.738
476
FSC002 Fascioliasis 44 0.738
477
c ACT075 Acute Myocardial Infarction 56 0.738
478
P KDN018 Kidney Disease 72 0.738
479
P RHB003 Rhabdomyosarcoma 66 0.738
480
GSG001 Gas Gangrene 52 0.738
481
ULC004 Ulcerative Colitis 74 0.738
482
CHR074 Choriocarcinoma 46 0.738
483
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 0.738
484
P PTT006 Pituitary Adenoma 55 0.738
485
TRC003 Trichomoniasis 53 0.738
486
ART016 Aortic Aneurysm 68 0.738
487
GLC008 Glucose Metabolism Disease 40 0.738
488
SCR001 Secretory Meningioma 40 0.738
489
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.738
490
LNG099 Lung Disease 62 0.738
491
P KRT007 Keratoconus 50 0.738
492
P CHR071 Charcot-Marie-Tooth Disease 64 0.738
493
P SPN046 Spinal Muscular Atrophy 63 0.738
494
KRT009 Keratosis 53 0.738
495
CLN015 Colon Adenocarcinoma 65 0.738
496
HMG005 Hemoglobinopathy 56 0.738
497
P MYS079 Miyoshi Muscular Dystrophy 54 0.738
498
P BND020 Bone Disease 59 0.738
499
TTH006 Tooth Disease 51 0.738
500
P PLY011 Polycystic Ovary Syndrome 57 0.738
501
P PRN023 Prion Disease 60 0.738
502
P PNC044 Pancreatitis 61 0.738
503
P EYD002 Eye Disease 57 0.738
504
P PRM002 Primary Hyperoxaluria 65 0.738
505
P OBS001 Obstructive Jaundice 48 0.738
506
IDP070 Idiopathic Scoliosis 42 0.738
507
FML035 Familial Hyperlipidemia 55 0.738
508
SPN021 Spinal Meningioma 50 0.738
509
P CRD246 Cardiovascular System Disease 56 0.738
510
HYP141 Hyperphenylalaninemia 42 0.738
511
P MYT002 Myotonic Dystrophy 51 0.738
512
NCL011 Nuclear Gene-Encoded Leigh Syndrome Spectrum 21 0.738
513
P TXP001 Toxoplasmosis 60 0.738
515
ANR040 Aneurysm 61 0.738
516
FST010 Fasting Hypoglycemia 33 0.738
517
HYP781 Hypoascorbemia 52 0.719
518
RHB024 Rhabdomyosarcoma 2 67 0.719
519
ANT039 Antisynthetase Syndrome 55 0.719
520
FST001 Foster-Kennedy Syndrome 39 0.719
521
FRC013 Fructose Utilization 15 0.639
522
PLY100 Polyploidy 36 0.639
523
ETH012 Ethylene Glycol Poisoning 29 0.639
524
c ACQ047 Acquired Methemoglobinemia 30 0.639
525
P RTT002 Rett Syndrome 79 0.639
526
c GLL024 Gallbladder Disease 1 52 0.639
527
MHR001 Mohr-Tranebjaerg Syndrome 49 0.639
528
P MTR004 Maturity-Onset Diabetes of the Young 68 0.639
529
DGL002 D-Glyceric Aciduria 41 0.639
530
MTC205 Mitochondrial Complex Iv Deficiency, Nuclear Type 1 57 0.639
531
HYP814 Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency 34 0.639
532
c MSC106 Mosaic Variegated Aneuploidy Syndrome 2 41 0.639
533
P INF037 Inflammatory Bowel Disease 53 0.639
534
DFF005 Diffuse Large B-Cell Lymphoma 54 0.639
535
LMB062 Limb Ischemia 55 0.639
536
INV001 Invasive Aspergillosis 49 0.639
537
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.639
538
MLD018 Mild Cognitive Impairment 48 0.639
539
DBT090 Diabetes and Deafness, Maternally Inherited 45 0.639
540
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.639
541
TRD006 Tardive Dyskinesia 53 0.639
542
WRN002 Wernicke-Korsakoff Syndrome 50 0.639
543
c HYP602 Hyperoxaluria, Primary, Type Ii 49 0.639
544
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.639
545
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.639
546
P SCL057 Scoliosis, Isolated 1 40 0.639
547
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 53 0.639
548
INC002 Inclusion Body Myositis 57 0.639
549
CMR002 Coumarin Resistance 59 0.639
550
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.639
551
ACH004 Achondroplasia 66 0.639
552
RHM034 Rahman Syndrome 37 0.639
553
c ACT073 Acute Leukemia 58 0.639
554
P ZLL001 Zellweger Syndrome 65 0.639
555
BRR002 Barrett's Adenocarcinoma 37 0.639
556
URM002 Uremia 47 0.639
557
CRC021 Carcinosarcoma 64 0.639
558
SKN019 Skin Melanoma 71 0.639
559
MSC193 Muscular Lipidosis 22 0.639
560
c PRG106 Progressive Muscular Dystrophy 32 0.639
561
PNC129 Pancreatic Adenocarcinoma 65 0.639
562
P EPL164 Epilepsy 68 0.639
563
P PLM036 Pulmonary Fibrosis 66 0.639
564
GST040 Gastric Adenocarcinoma 67 0.639
565
ANV001 Anovulation 47 0.639
566
OVR063 Overnutrition 42 0.639
567
P BNG002 Benign Meningioma 36 0.639
568
PPT005 Peptic Ulcer Disease 58 0.639
569
P PLL002 Pellagra 46 0.639
570
P ART022 Arthritis 71 0.639
571
OST012 Osteoarthritis 77 0.639
572
P INT070 Intestinal Obstruction 57 0.639
573
P DNG005 Dengue Virus 56 0.639
574
SPR006 Sparganosis 35 0.639
575
P DMN002 Dementia 66 0.639
576
ALL029 Allergic Disease 59 0.639
577
VRC001 Varicocele 48 0.639
578
PCD001 Pica Disease 38 0.639
579
SKN005 Skin Atrophy 41 0.639
580
NRT004 Neuritis 53 0.639
581
P HYP086 Hypothyroidism 69 0.639
582
GLN002 Glanders 38 0.639
583
GST033 Gestational Diabetes 61 0.639
584
MST005 Mastitis 53 0.639
585
P FNC004 Fanconi Syndrome 60 0.639
586
BRN024 Bronchitis 67 0.639
587
P CWD010 Cowden Syndrome 70 0.639
588
NRT001 Neurotic Disorder 56 0.639
589
P RTN018 Retinal Disease 53 0.639
590
ACT058 Active Peptic Ulcer Disease 56 0.639
591
MDD011 Mood Disorder 62 0.639
592
P GLM007 Glomerulonephritis 60 0.639
593
DMY004 Demyelinating Disease 50 0.639
594
P PLY019 Polyneuropathy 52 0.639
595
GST023 Gastric Ulcer 52 0.639
596
QDR001 Quadriplegia 50 0.639
597
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.639
598
c HPT016 Hepatitis B 62 0.639
599
GRN017 Granulocytopenia 42 0.639
600
SYS003 Systolic Heart Failure 49 0.639
601
P DRM053 Dermatitis, Atopic 65 0.522
602
c ALP101 Alpha-Thalassemia 62 0.522
603
c LCT020 Lactic Acidosis, Chronic Adult Form 8 0.522
605
MTH047 Methanol Poisoning 37 0.522
606
CNG506 Congenital Amyoplasia 27 0.522
607
GRN033 Granulomatous Mastitis 32 0.522
608
GLM044 Glomerular Disease 35 0.522
609
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.522
610
P NSP012 Nasopharyngeal Carcinoma 61 0.522
611
CHR696 Charcot-Marie-Tooth Disease, X-Linked Recessive, 4, with or Without Cerebellar Ataxia 32 0.522
612
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.522
613
3HY007 3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency 51 0.522
614
P MYS003 Myasthenia Gravis 68 0.522
615
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 59 0.522
616
c SPS222 Spastic Paraplegia 20, Autosomal Recessive 56 0.522
617
SQM013 Squamous Cell Carcinoma, Head and Neck 73 0.522
618
P ALB003 Albinism-Deafness Syndrome 34 0.522
619
CMB017 Combined Oxidative Phosphorylation Deficiency 6 41 0.522
620
CRD223 Cardiac Arrhythmia 63 0.522
621
ANR007 Anorexia Nervosa 60 0.522
622
ALL003 Allergic Rhinitis 67 0.522
623
c CTR132 Cataract 3, Multiple Types 42 0.522
624
PRK088 Parkinson Disease, Mitochondrial 19 0.522
625
MTC029 Mitochondrial Complex V Deficiency, Nuclear Type 1 40 0.522
626
END057 Endometrial Cancer 72 0.522
627
P TRC072 Treacher Collins Syndrome 1 62 0.522
628
HMF006 Hemifacial Microsomia 55 0.522
629
PHS025 Phosphatase, Acid, of Tissues 28 0.522
630
CRT072 Creutzfeldt-Jakob Disease 68 0.522
631
CRZ001 Crouzon Syndrome 65 0.522
632
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.522
633
c LKM063 Leukemia, Chronic Myeloid 71 0.522
634
CHR100 Chronic Ulcer of Skin 57 0.522
635
EPD015 Epidemic Typhus 44 0.522
637
P FML011 Familial Adenomatous Polyposis 71 0.522
638
VTM002 Vitamin B12 Deficiency 48 0.522
639
P PRG013 Paraganglioma 57 0.522
640
CRB150 Cerebral Creatine Deficiency Syndrome 2 54 0.522
641
PYR012 Pyruvate Dehydrogenase E1-Beta Deficiency 41 0.522
642
PRT251 Proteinuria, Chronic Benign 57 0.522
643
NRN005 Neuronal Ceroid-Lipofuscinoses 61 0.522
644
BCT021 Bacterial Sepsis 43 0.522
645
P HYP111 Hyperprolinemia 45 0.522
646
P PLY014 Polycystic Kidney Disease 69 0.522
647
P ATR011 Atrial Fibrillation 66 0.522
648
P FTL001 Fetal Alcohol Syndrome 55 0.522
649
CRD231 Cardiomyopathy, Infantile Histiocytoid 45 0.522
650
SLF014 Sulfite Oxidase Deficiency, Isolated 53 0.522
651
CNT105 Central Core Disease of Muscle 59 0.522
652
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 0.522
653
P MCR129 Microvascular Complications of Diabetes 1 68 0.522
654
c MTH083 Methemoglobinemia, Beta Type 22 0.522
655
c MTH084 Methemoglobinemia, Alpha Type 11 0.522
656
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.522
657
EWN003 Ewing Sarcoma 70 0.522
658
P MJR001 Major Depressive Disorder 68 0.522
659
ACT119 Acute Promyelocytic Leukemia 62 0.522
660
c BRS111 Breast-Ovarian Cancer, Familial 2 53 0.522
661
c SCH079 Schizophrenia 1 44 0.522
662
TBL029 Tubulin, Beta 28 0.522
663
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.522
664
c HYP597 Hyperprolinemia, Type Ii 43 0.522
665
P TRT019 Torticollis 47 0.522
666
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 0.522
667
KRT071 Keratosis, Seborrheic 56 0.522
668
PTR032 Peters-Plus Syndrome 63 0.522
669
RFS006 Refsum Disease, Classic 63 0.522
670
c TBR025 Tuberous Sclerosis 1 84 0.522
671
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 69 0.522
672
c SML038 Small Cell Cancer of the Lung 69 0.522
673
P HYP726 Hypercalcemia, Infantile, 1 58 0.522
674
P HYP750 Hypertriglyceridemia, Familial 62 0.522
675
MLT157 Multiple System Atrophy 1 69 0.522
676
P MDL005 Medulloblastoma 75 0.522
677
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.522
678
P MYP105 Myopathy, Myosin Storage, Autosomal Dominant 40 0.522
679
c CHR489 Charcot-Marie-Tooth Disease, Axonal, Type 2q 32 0.522
680
MLD001 Melioidosis 67 0.522
681
MTC155 Mitochondrial Complex I Deficiency, Nuclear Type 7 22 0.522
682
CHR431 Chronic Venous Insufficiency 48 0.522
683
CRD137 Cardiogenic Shock 56 0.522
684
P NRD007 Neurodegeneration with Brain Iron Accumulation 52 0.522
685
c CHR697 Charcot-Marie-Tooth Disease X-Linked Recessive 4 31 0.522
686
P HRD144 Hereditary Mixed Polyposis Syndrome 54 0.522
687
RGD003 Rigid Spine Muscular Dystrophy 1 56 0.522
688
LMY002 Leiomyoma 51 0.522
689
P FML068 Familial Hypocalciuric Hypercalcemia 55 0.522
690
FBR009 Fibrous Dysplasia 48 0.522
691
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.522
692
P SDR003 Sideroblastic Anemia 51 0.522
693
SCT002 Scotoma 42 0.522
694
P HLP001 Holoprosencephaly 69 0.522
695
NTR005 Nutritional Deficiency Disease 61 0.522
696
URT010 Ureteral Obstruction 45 0.522
697
P EMB005 Embryonal Rhabdomyosarcoma 53 0.522
698
INT007 Intermediate Coronary Syndrome 54 0.522
699
DRM011 Dermatophytosis 52 0.522
700
BLT006 Bilateral Breast Cancer 48 0.522
701
GLY085 Glycogen Storage Disease Due to Lactate Dehydrogenase Deficiency 16 0.522
702
EMR021 Emery-Dreifuss Syndrome 11 0.522
703
c VRL010 Viral Hepatitis 53 0.522
704
MNT002 Mental Depression 57 0.522
705
PSD009 Pseudohermaphroditism 46 0.522
706
PYD002 Pyoderma 50 0.522
707
MLG077 Malignant Peripheral Nerve Sheath Tumor 54 0.522
708
ACQ007 Acquired Immunodeficiency Syndrome 59 0.522
709
ILS001 Ileus 50 0.522
710
NPH009 Nephrolithiasis 54 0.522
711
TNC002 Tinea Capitis 42 0.522
712
CMB007 Combined Immunodeficiency 57 0.522
713
P VNS003 Venous Insufficiency 55 0.522
714
c MCR112 Microvascular Complications of Diabetes 2 42 0.522
715
c DVL110 Developmental and Epileptic Encephalopathy 88 20 0.522
716
P MGR003 Migraine with Aura 52 0.522
717
OST003 Osteonecrosis 61 0.522
718
ANT018 Anthracosis 51 0.522
719
OST011 Osteomalacia 52 0.522
720
P MGR001 Migraine Without Aura 49 0.522
721
ALC010 Alcoholic Cardiomyopathy 42 0.522
722
GT001 Gout 64 0.522
723
DNG003 Dengue Disease 65 0.522
724
CRY005 Cryptococcosis 60 0.522
725
GTR002 Goiter 53 0.522
726
FLR001 Filarial Elephantiasis 59 0.522
727
PNC001 Pancytopenia 53 0.522
728
CRT012 Cortical Blindness 42 0.522
729
NRX001 Neuroaxonal Dystrophy 38 0.522
730
P NRN021 Neuronal Ceroid Lipofuscinosis 65 0.522
731
RYS001 Reye Syndrome 49 0.522
732
c ATM011 Autoimmune Hepatitis 63 0.522
733
P CRN037 Craniosynostosis 68 0.522
734
P TBR001 Tuberous Sclerosis 69 0.522
735
P LNG028 Long Qt Syndrome 64 0.522
736
P END044 Endometriosis 62 0.522
737
ING001 Inguinal Hernia 59 0.522
738
P MTC010 Mitochondrial Dna Depletion Syndrome 47 0.522
739
LPR001 Lepromatous Leprosy 49 0.522
740
HMP005 Hemiplegia 54 0.522
741
VTM033 Vitamin K Deficiency Bleeding 48 0.522
742
MCR013 Microphthalmia 60 0.522
743
c INH020 Inherited Metabolic Disorder 48 0.522
744
P PSD003 Pseudohypoaldosteronism 44 0.522
745
P SLP005 Sleep Disorder 61 0.522
746
P AXN001 Axonal Neuropathy 35 0.522
747
CCN002 Cocaine Abuse 49 0.522
748
P TRT010 Teratoma 51 0.522
749
INT066 Interstitial Lung Disease 60 0.522
750
MLG067 Malignant Giant Cell Tumor 28 0.522
751
P MTR014 Motor Neuron Disease 65 0.522
752
P TMP001 Temporal Lobe Epilepsy 49 0.522
753
BRS051 Breast Disease 58 0.522
754
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.522
755
LYS002 Lysosomal Storage Disease 51 0.522
756
AMN001 Amenorrhea 54 0.522
757
KLB003 Klebsiella Pneumonia 50 0.522
758
OPS001 Opisthorchiasis 41 0.522
759
DBT002 Diabetic Autonomic Neuropathy 41 0.522
760
LCH001 Leech Infestation 38 0.522
761
MYS004 Myiasis 39 0.522
762
HYP080 Hypogonadism 50 0.522
763
PST028 Post-Traumatic Stress Disorder 59 0.522
764
BBS001 Babesiosis 49 0.522
765
INV005 Inverted Follicular Keratosis 32 0.522
766
P NRF002 Neurofibromatosis 57 0.522
767
DST006 Diastolic Heart Failure 45 0.522
768
HYD005 Hydrocele 46 0.522
769
TTR005 Tetrahydrobiopterin Deficiency 48 0.522
770
P RDC010 Reducing Body Myopathy 33 0.522
771
DPR016 Depression 65 0.522
772
P CRB088 Cerebral Atrophy 33 0.522
773
MYT011 Myotonia 39 0.522
774
OVR094 Ovarian Epithelial Cancer 39 0.522
775
GST039 Gastroduodenitis 37 0.522
776
LYM133 Lymphoma, Hodgkin, Classic 74 0.369
777
SPN050 Spinocerebellar Degeneration 39 0.369
778
CLF004 Cleft Lip/palate 57 0.369
779
P OTT001 Otitis Externa 42 0.369
780
c BCT007 Bacterial Meningitis 55 0.369
781
SCL025 Scleromyxedema 32 0.369
782
VNZ002 Venezuelan Equine Encephalitis 46 0.369
783
SLN002 Selenium Poisoning 10 0.369
784
CNN002 Cannabis Abuse 45 0.369
785
c INF185 Infantile Epilepsy Syndrome 29 0.369
786
RFR010 Refractory Anemia 49 0.369
787
ACT181 Acute Motor Axonal Neuropathy 22 0.369
788
MTB016 Metabolic Myopathy 30 0.369
789
IDP079 Idiopathic Dropped Head Syndrome 10 0.369
790
BNG077 Benign Idiopathic Neonatal Seizures 23 0.369
791
NRM022 Neurometabolic Disease 24 0.369
792
CCN009 Cocaine Intoxication 30 0.369
793
PRC051 Paracetamol Poisoning 29 0.369
794
c ADL084 Adult-Onset Myasthenia Gravis 21 0.369
795
SPS019 Spastic Paraparesis 38 0.369
796
SDD008 Sudden Sensorineural Hearing Loss 41 0.369
797
GNT167 Genetic Obesity 30 0.369
798
THY128 Thyroid Tumor 35 0.369
799
c AMY088 Amyotrophic Lateral Sclerosis 3 31 0.369
800
c ART068 Aortic Aneurysm, Familial Thoracic 2 33 0.369
801
EPL050 Epilepsy, Partial, with Pericentral Spikes 26 0.369
802
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 58 0.369
803
SPP011 Suppression of Tumorigenicity 12 61 0.369
804
PLM061 Pulmonary Edema of Mountaineers 26 0.369
805
c SCL052 Scleroderma, Familial Progressive 61 0.369
806
P DNT020 Dent Disease 1 63 0.369
807
DNN001 Danon Disease 59 0.369
808
MSC152 Muscular Dystrophy, Becker Type 69 0.369
809
MTC147 Mitochondrial Complex I Deficiency, Nuclear Type 12 21 0.369
810
CRD132 Cardiac Conduction Defect 60 0.369
811
c MCL013 Mucolipidosis Iv 65 0.369
812
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 64 0.369
813
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.369
814
ALK013 Alkaptonuria 59 0.369
815
FBR012 Fabry Disease 70 0.369
816
KFR001 Kufor-Rakeb Syndrome 59 0.369
817
SNS008 Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis 60 0.369
818
MTC149 Mitochondrial Complex I Deficiency, Mitochondrial Type 1 14 0.369
819
c NPH049 Nephrotic Syndrome, Type 2 51 0.369
820
P SPR120 Supranuclear Palsy, Progressive, 1 69 0.369
821
ENC055 Encephalopathy, Ethylmalonic 51 0.369
822
PRS127 Pearson Marrow-Pancreas Syndrome 52 0.369
823
c MTR020 Maturity-Onset Diabetes of the Young, Type 3 54 0.369
824
P D2H002 D-2-Hydroxyglutaric Aciduria 1 52 0.369
825
ASC010 Ascaris Lumbricoides Infection 49 0.369
826
P RHM011 Rheumatoid Arthritis 82 0.369
827
HRD029 Hereditary Leiomyomatosis and Renal Cell Cancer 56 0.369
828
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 68 0.369
829
P OST002 Osteoporosis 76 0.369
830
P LKM071 Leukemia, Chronic Lymphocytic 75 0.369
831
CLF027 Cleft Palate, Isolated 64 0.369
832
c SPN225 Spondyloarthropathy 1 70 0.369
833
c SYN084 Synpolydactyly 1 36 0.369
834
SYR010 Syringomyelia, Noncommunicating Isolated 36 0.369
835
c THR092 Thrombophilia Due to Thrombin Defect 74 0.369
836
ARG007 Argininemia 58 0.369
837
CYS019 Cystathioninuria 46 0.369
838
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 63 0.369
839
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.369
840
SRB001 Sorbitol Dehydrogenase Deficiency with Peripheral Neuropathy 21 0.369
841
c FNC066 Fanconi Renotubular Syndrome 5 27 0.369
842
ADR016 Adrenal Cortical Carcinoma 62 0.369
843
P LSS002 Lissencephaly 50 0.369
844
END014 Endemic Typhus 32 0.369
845
HYP017 Hypophosphatemia 49 0.369
846
CRR001 Carrion's Disease 31 0.369
847
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.369
848
DSR012 Disordered Steroidogenesis Due to Cytochrome P450 Oxidoreductase Deficiency 39 0.369
849
c LBR006 Leber Congenital Amaurosis 11 35 0.369
850
P MGL010 Megalencephalic Leukoencephalopathy with Subcortical Cysts 2a 40 0.369
851
c BTT014 Beta-Thalassemia 72 0.369
852
MYL009 Myelodysplastic Syndrome 67 0.369
853
P HRD021 Hereditary Sensory Neuropathy 48 0.369
854
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.369
855
c RTN143 Retinitis Pigmentosa 47 41 0.369
856
HRS016 Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction 26 0.369
857
P HMG032 Hemoglobin H Disease 51 0.369
858
MLT150 Multiple Mitochondrial Dysfunctions Syndrome 2 with Hyperglycinemia 36 0.369
859
HMN002 Human Granulocytic Anaplasmosis 31 0.369
860
RCK002 Rocky Mountain Spotted Fever 34 0.369
861
P MCL001 Mucolipidosis 49 0.369
862
THY121 Thyroid Gland Anaplastic Carcinoma 67 0.369
863
ADT001 Auditory Agnosia 26 0.369
864
CRT007 Cortical Deafness 26 0.369
865
HMN047 Human Cytomegalovirus Infection 57 0.369
866
c HRD201 Hereditary Sensory and Autonomic Neuropathy Type 1 43 0.369
867
OLG022 Oligoasthenoteratozoospermia 36 0.369
868
c 3MT007 3-Methylglutaconic Aciduria 37 0.369
869
PLL012 Pollen Allergy 45 0.369
870
PHY002 Physical Disorder 41 0.369
871
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.369
872
P LYM118 Lymphoma 67 0.369
873
HYP025 Hyperphosphatemia 48 0.369
874
c PRM032 Primary Congenital Glaucoma 41 0.369
875
TNS007 Taeniasis 46 0.369
876
INT017 Intestinal Schistosomiasis 51 0.369
877
P MYF003 Myofibrillar Myopathy 49 0.369
878
PYR022 Pyruvate Dehydrogenase E1-Alpha Deficiency 64 0.369
879
c DFN251 Deafness, Autosomal Dominant 11 44 0.369
880
c HYP839 Hyperlipidemia, Familial Combined, 1 30 0.369
881
c PRX059 Peroxisome Biogenesis Disorder 1a 56 0.369
882
CYS044 Cystic Disease of Lung 20 0.369
883
c GLC112 Galactosemia Iii 51 0.369
884
P HYP768 Hyperlipoproteinemia, Type I 67 0.369
885
c GRV008 Graves Disease 1 54 0.369
886
MYC079 Myoclonic Epilepsy of Lafora 64 0.369
887
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.369
888
SPN354 Spinal Arachnoiditis 36 0.369
889
CTY001 Cat Eye Syndrome 44 0.369
890
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.369
891
c PRT132 Protoporphyria, Erythropoietic, 1 61 0.369
892
P PLV020 Pelvic Organ Prolapse 58 0.369
893
KRT019 Keratitis, Hereditary 66 0.369
894
KPS004 Kaposi Sarcoma 77 0.369
895
GRG001 Greig Cephalopolysyndactyly Syndrome 64 0.369
896
EXF001 Exfoliation Syndrome 56 0.369
897
CHD004 Chudley-Mccullough Syndrome 48 0.369
898
c TTH012 Tooth Agenesis, Selective, 3 25 0.369
899
P ORT004 Orthostatic Intolerance 63 0.369
900
LTN004 Late-Onset Retinal Degeneration 60 0.369
901
c TTH011 Tooth Agenesis, Selective, 2 13 0.369
902
c LNG048 Long Qt Syndrome 3 53 0.369
903
c MLT068 Multiple Mitochondrial Dysfunctions Syndrome 1 45 0.369
904
LYM143 Lymphoma, Non-Hodgkin, Familial 75 0.369
905
PHL006 Phelan-Mcdermid Syndrome 60 0.369
906
c LNG047 Long Qt Syndrome 2 59 0.369
907
c ART101 Aortic Valve Disease 2 66 0.369
908
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 66 0.369
909
MYP099 Myopathy, Isolated Mitochondrial, Autosomal Dominant 27 0.369
910
AKL001 Au-Kline Syndrome 39 0.369
911
HRT037 Heart and Brain Malformation Syndrome 31 0.369
912
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 0.369
913
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 0.369
914
INT258 Interstitial Nephritis, Karyomegalic 45 0.369
915
c RTN140 Retinitis Pigmentosa 67 32 0.369
916
c DFN360 Deafness, Autosomal Dominant 69 34 0.369
917
c MCR312 Microphthalmia, Syndromic 10 40 0.369
918
HRN029 Hearing Loss, Noise-Induced 37 0.369
920
WST005 West Nile Virus 57 0.369
921
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.369
922
2MN001 2-Aminoadipic 2-Oxoadipic Aciduria 34 0.369
923
PRP083 Porphyria, Acute Intermittent 65 0.369
924
c NTR047 Neutropenia, Severe Congenital, 1, Autosomal Dominant 37 0.369
925
MLL018 Miller-Dieker Lissencephaly Syndrome 52 0.369
926
MTC207 Mitochondrial Complex Ii Deficiency, Nuclear Type 1 55 0.369
927
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.369
928
c MTC056 Mitochondrial Dna Depletion Syndrome 4a 62 0.369
929
LWC002 Lowe Oculocerebrorenal Syndrome 68 0.369
930
LGN006 Legionnaire Disease 52 0.369
931
c MYC058 Myocardial Infarction 2 24 0.369
932
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.369
933
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.369
934
ENT011 Enterocolitis 55 0.369
935
c GLY008 Glycogen Storage Disease Ii 72 0.369
936
HLT002 Halothane Hepatitis 31 0.369
937
P HYP058 Hypervitaminosis a 47 0.369
938
HYP784 Hypogonadism, Male 43 0.369
939
TRG002 Trigeminal Neuralgia 61 0.369
940
CRN295 Carnitine Palmitoyltransferase I Deficiency 55 0.369
941
MYP091 Myopathy, Congenital, with Fiber-Type Disproportion 43 0.369
942
MYL013 Myeloperoxidase Deficiency 44 0.369
943
c PRD040 Periodontitis, Chronic 52 0.369
944
PLY001 Polycythemia Vera 69 0.369
945
MYC080 Myoclonic Epilepsy of Unverricht and Lundborg 53 0.369
946
MYP097 Myopathy with Lactic Acidosis, Hereditary 31 0.369
947
c NPH055 Nephrotic Syndrome, Type 1 52 0.369
948
P TTR001 Tetralogy of Fallot 69 0.369
949
WLF001 Wolff-Parkinson-White Syndrome 65