Search results for NADPH

1522 hits were found for NADPH

# Family MCID Name MIFTS Score
1
P CHR012 Chronic Granulomatous Disease 69 21.221
2
HYP266 Hypoxia 57 11.541
3
MTH072 Methemoglobin Reductase Deficiency 15 11.104
4
c MCR130 Microvascular Complications of Diabetes 6 41 10.964
5
c MCR120 Microvascular Complications of Diabetes 7 47 10.964
6
c MCR113 Microvascular Complications of Diabetes 3 52 10.964
7
c MCR133 Microvascular Complications of Diabetes 4 41 10.964
8
HYP066 Hyperglycemia 61 10.105
9
ATH013 Atherosclerosis Susceptibility 63 8.656
10
P VSC007 Vascular Disease 63 8.283
11
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 7.832
12
ISC004 Ischemia 61 7.610
13
P PLM037 Pulmonary Hypertension 72 7.595
14
c MCR115 Microvascular Complications of Diabetes 5 65 7.539
15
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 7.377
16
PRT251 Proteinuria, Chronic Benign 57 7.180
17
AGN016 Aging 54 7.040
18
PRT037 Pertussis 65 6.847
19
CRB004 Cerebral Artery Occlusion 45 6.562
20
P SLP006 Sleep Apnea 69 6.529
21
BRN071 Brain Injury 50 6.301
22
GLC009 Glucosephosphate Dehydrogenase Deficiency 53 6.093
23
NNL005 Non-Alcoholic Fatty Liver Disease 63 6.015
24
P HNT016 Huntington Disease 73 5.987
25
IMP005 Impotence 52 5.758
26
P PLM036 Pulmonary Fibrosis 66 5.631
27
CYT002 Cytokine Deficiency 43 5.570
28
c HYP836 Hypercholesterolemia, Familial, 1 73 5.531
29
P NRB001 Neuroblastoma 66 5.531
30
TRM010 Traumatic Brain Injury 51 5.481
31
47X002 47,xyy 48 5.460
32
RNL077 Renal Fibrosis 46 5.367
33
BCT022 Bacterial Infectious Disease 56 5.314
34
GRN051 Granulomatous Disease, Chronic, X-Linked 57 5.231
35
ANX004 Anoxia 40 5.167
36
c PRC016 Pre-Eclampsia 65 5.117
37
FTT001 Fatty Liver Disease 62 5.040
38
RPD005 Rapidly Involuting Congenital Hemangioma 46 4.996
39
48X005 48,xyyy 39 4.902
40
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 4.808
41
P LTR001 Lateral Sclerosis 58 4.805
42
c AMY091 Amyotrophic Lateral Sclerosis 1 88 4.786
43
NNL006 Non-Alcoholic Steatohepatitis 54 4.750
44
c ATR087 Atrial Standstill 1 74 4.741
45
HMC014 Homocysteinemia 52 4.732
46
HLX001 Helix Syndrome 48 4.658
47
SPN186 Spinal Cord Injury 61 4.569
48
CLT003 Colitis 63 4.505
49
c PLM164 Pulmonary Hypertension, Primary, 1 76 4.428
50
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 4.404
51
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 4.380
52
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 4.380
53
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 4.380
54
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 4.380
55
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 4.380
56
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 4.380
57
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 4.380
58
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 4.380
59
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 4.380
60
ALL014 Allergic Encephalomyelitis 34 4.378
61
P ASP006 Aspergillosis 72 4.367
62
GLB002 Glioblastoma 67 4.358
63
P ADL010 Adult Respiratory Distress Syndrome 71 4.358
64
P KDN018 Kidney Disease 72 4.330
65
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 4.272
66
P ADN016 Adenocarcinoma 63 4.269
67
CHL014 Cholera 62 4.233
68
c GRN062 Granulomatous Disease, Chronic, Autosomal Recessive, 1 46 4.212
69
c GRN061 Granulomatous Disease, Chronic, Autosomal Recessive, 4 48 4.212
70
LPD008 Lipid Metabolism Disorder 62 4.174
71
BRN004 Brain Edema 54 4.127
72
c LKM061 Leukemia, Acute Myeloid 83 4.122
73
ART140 Arteries, Anomalies of 53 4.083
74
GLM045 Glioma 63 4.067
75
P INF037 Inflammatory Bowel Disease 53 4.052
76
P MYC084 Mycobacterium Tuberculosis 1 68 4.049
77
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 4.031
78
LPP008 Lipoprotein Quantitative Trait Locus 65 4.013
79
CYT014 Cytochrome P450 Oxidoreductase Deficiency 34 3.968
80
GLL048 Glial Tumor 52 3.960
81
c HYP595 Hypertension, Essential 85 3.947
82
P PNC035 Pancreatic Cancer 86 3.925
83
PLM134 Pulmonary Fibrosis, Idiopathic 76 3.904
84
ATM095 Autoimmune Disease 61 3.899
85
CHG001 Chagas Disease 66 3.895
86
P SCK005 Sickle Cell Disease 56 3.894
87
LNG099 Lung Disease 62 3.871
88
c CHR684 Chronic Kidney Disease 69 3.813
89
P ALZ034 Alzheimer Disease 87 3.777
90
P HML002 Hemolytic Anemia 62 3.762
91
RTN020 Retinal Vascular Disease 46 3.756
92
HYP060 Hyperinsulinism 54 3.730
93
CRB039 Cerebrovascular Disease 66 3.727
94
PLY150 Polykaryocytosis Inducer 29 3.722
95
END086 End Stage Renal Disease 52 3.722
96
P LVR013 Liver Disease 69 3.681
97
P MYL006 Myeloid Leukemia 61 3.632
98
P MYC007 Myocardial Infarction 70 3.627
99
STR067 Stroke, Ischemic 80 3.607
100
P HYP086 Hypothyroidism 69 3.607
101
c ACT027 Acute Pancreatitis 60 3.603
102
c TYP009 Type 2 Diabetes Mellitus 92 3.566
103
ART016 Aortic Aneurysm 68 3.553
104
CYS001 Cystic Fibrosis 78 3.517
105
GLC003 Glucose Intolerance 54 3.511
106
P MSC005 Muscular Dystrophy 67 3.502
107
P PRK039 Parkinsonism 55 3.473
108
CHL068 Cholestasis 61 3.449
109
P KLZ004 Kala-Azar 1 41 3.440
110
LSH001 Leishmaniasis 64 3.440
111
CNG034 Congestive Heart Failure 69 3.425
112
PPL052 Papillomatosis, Confluent and Reticulated 34 3.423
113
TXC005 Toxic Shock Syndrome 62 3.418
115
BNR002 Bone Resorption Disease 47 3.400
116
P PNC044 Pancreatitis 61 3.398
117
STT001 Status Epilepticus 59 3.398
118
c DNT047 Dentinogenesis Imperfecta Type 2 35 3.390
119
SKN016 Skin Disease 63 3.371
120
P MLN008 Melanoma 76 3.371
121
PST092 Posttransplant Acute Limbic Encephalitis 28 3.367
122
ANR040 Aneurysm 61 3.339
123
P ART021 Arteriosclerosis 54 3.324
124
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 3.299
125
P HRS035 Hirschsprung Disease 1 66 3.273
126
INV001 Invasive Aspergillosis 49 3.273
127
P ATR011 Atrial Fibrillation 66 3.247
128
PRS045 Prostatic Hypertrophy 53 3.234
129
P HPT023 Hepatocellular Carcinoma 96 3.196
130
PRT036 Peritonitis 65 3.196
131
P NSP012 Nasopharyngeal Carcinoma 61 3.146
132
ALL006 Allergic Asthma 56 3.138
133
ULC004 Ulcerative Colitis 74 3.138
134
NPH009 Nephrolithiasis 54 3.138
135
PRS129 Prostatic Hyperplasia, Benign 49 3.116
136
PRS021 Prostatic Adenoma 43 3.116
137
HYP014 Hyperuricemia 51 3.087
138
P DBT009 Diabetes Mellitus 67 3.082
139
c GRN064 Granulomatous Disease, Chronic, Autosomal Recessive, 3 36 3.070
140
ALL029 Allergic Disease 59 3.064
141
P BCL017 B-Cell Lymphoma 59 3.054
142
URT010 Ureteral Obstruction 45 3.054
143
P MCR129 Microvascular Complications of Diabetes 1 68 3.030
144
c MCR112 Microvascular Complications of Diabetes 2 42 3.030
145
c DLT002 Dilated Cardiomyopathy 78 3.018
146
c SCL052 Scleroderma, Familial Progressive 61 3.003
147
P PHC003 Pheochromocytoma 69 2.996
148
ADR040 Adrenal Gland Pheochromocytoma 46 2.996
149
P PRK057 Parkinson Disease, Late-Onset 80 2.994
150
HLC007 Helicobacter Pylori Infection 67 2.985
151
RNL114 Renal Cell Carcinoma, Nonpapillary 80 2.979
152
HYP056 Hypoglycemia 65 2.974
153
DBT010 Diabetic Neuropathy 54 2.951
154
c TYP008 Type 1 Diabetes Mellitus 70 2.920
155
BRR014 Barrett Esophagus 66 2.913
156
HYP572 Hypoganglionosis 27 2.891
157
P PNM007 Pneumonia 67 2.890
158
P GST053 Gastric Cancer 83 2.867
159
P CRD246 Cardiovascular System Disease 56 2.862
161
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.834
162
P ECL001 Eclampsia 52 2.831
163
THR024 Thrombosis 56 2.819
164
P ENC018 Encephalopathy 62 2.809
165
PLM129 Pulmonary Disease, Chronic Obstructive 74 2.807
166
P MSC003 Muscular Atrophy 52 2.801
167
P RTN016 Retinal Degeneration 52 2.801
168
TRN015 Transient Cerebral Ischemia 63 2.801
169
THY029 Thyroid Carcinoma 51 2.799
170
CHL123 Chlamydia 58 2.781
171
P ART022 Arthritis 71 2.775
172
OST012 Osteoarthritis 77 2.775
173
P LPS004 Lupus Erythematosus 61 2.774
174
PNC041 Pancreatic Ductal Adenocarcinoma 51 2.764
175
MSC007 Muscle Hypertrophy 64 2.746
176
P HYP076 Hyperthyroidism 53 2.746
177
P ALC033 Alcohol Use Disorder 61 2.740
178
ACT119 Acute Promyelocytic Leukemia 62 2.737
179
CRH001 Crohn's Disease 80 2.725
180
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 2.715
181
P GLM007 Glomerulonephritis 60 2.715
182
c CNG006 Congenital Hypothyroidism 63 2.691
183
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 2.684
184
P SKN015 Skin Carcinoma 71 2.684
185
c EXD008 Exudative Vitreoretinopathy 1 71 2.671
186
DFC004 Deficiency Anemia 74 2.671
187
MLR004 Malaria 80 2.653
188
HPT004 Hepatic Coma 43 2.653
189
P MYP004 Myopathy 67 2.653
190
HPT019 Hepatic Encephalopathy 59 2.653
191
P PRP019 Peripheral Nervous System Disease 58 2.653
192
c PCH010 Pachyonychia Congenita 3 43 2.638
193
P GST044 Gastritis 55 2.635
194
P HYP750 Hypertriglyceridemia, Familial 62 2.621
196
P FBR017 Fibrosarcoma 56 2.599
197
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 60 2.588
198
P PRD008 Periodontitis 64 2.588
199
P LKM002 Leukemia 67 2.588
200
PRT013 Portal Hypertension 59 2.588
201
INS024 Insulin-Like Growth Factor I 78 2.577
202
P CLR023 Colorectal Cancer 100 2.577
203
P RRH023 Rare Hereditary Hemochromatosis 54 2.577
204
HMS001 Hemosiderosis 48 2.577
205
HPT022 Hepatoblastoma 54 2.568
206
P RTN018 Retinal Disease 53 2.561
207
MYL013 Myeloperoxidase Deficiency 44 2.555
208
PNC129 Pancreatic Adenocarcinoma 65 2.555
209
24D001 2,4-Dienoyl-Coa Reductase Deficiency 34 2.544
210
c GRN063 Granulomatous Disease, Chronic, Autosomal Recessive, 2 39 2.539
211
DSR012 Disordered Steroidogenesis Due to Cytochrome P450 Oxidoreductase Deficiency 39 2.522
212
P RNV001 Renovascular Hypertension 49 2.522
213
P BLD134 Bladder Cancer 79 2.515
214
P HRT032 Heart Disease 81 2.515
215
LVR012 Liver Cirrhosis 63 2.515
216
P RHM011 Rheumatoid Arthritis 82 2.487
217
P VSC011 Vasculitis 61 2.487
218
P NRP001 Neuropathy 60 2.487
219
P NTR004 Neutropenia 63 2.487
220
P OST002 Osteoporosis 76 2.484
221
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 2.484
222
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 2.484
223
P CTR002 Cataract 60 2.483
224
ATS010 Autosomal Recessive Disease 42 2.459
225
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 50 2.457
226
MSC157 Muscular Dystrophy, Duchenne Type 79 2.450
227
P PRN023 Prion Disease 60 2.443
228
PRP027 Peripheral Vascular Disease 71 2.420
229
END057 Endometrial Cancer 72 2.416
230
OST159 Osteogenic Sarcoma 66 2.416
231
APN008 Apnea, Obstructive Sleep 67 2.414
232
HMN044 Human Immunodeficiency Virus Type 1 78 2.383
233
c ACT071 Acute Kidney Failure 60 2.383
234
IMM167 Immune Deficiency Disease 78 2.366
235
TLN003 Telangiectasis 51 2.366
236
c HPT073 Hepatitis C Virus 71 2.359
237
P HRD144 Hereditary Mixed Polyposis Syndrome 54 2.353
238
P INF038 Influenza 68 2.349
239
P INF032 Infertility 57 2.349
240
SQM006 Squamous Cell Carcinoma 60 2.349
241
c SYS001 Systemic Lupus Erythematosus 87 2.342
242
CRT015 Carotid Artery Occlusion 45 2.342
243
P AST005 Asthma 76 2.314
244
c LKM063 Leukemia, Chronic Myeloid 71 2.314
245
P MYC008 Myocarditis 59 2.314
246
INT323 Intraocular Pressure Quantitative Trait Locus 64 2.304
247
P MLT020 Multiple Sclerosis 79 2.299
248
ADN018 Adenoma 59 2.299
249
P SLM003 Salmonellosis 54 2.265
250
PRV004 Periventricular Leukomalacia 52 2.265
251
GST092 Gastroesophageal Reflux 61 2.257
252
c HPT001 Hepatitis C 62 2.257
253
PST011 Pustulosis of Palm and Sole 52 2.257
254
RTN003 Retinal Ischemia 49 2.257
255
PRP016 Paraplegia 52 2.242
256
IRN002 Iron Metabolism Disease 57 2.242
257
P LNG032 Lung Cancer 98 2.237
258
P CRN300 Coronary Heart Disease 1 73 2.237
259
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 2.224
260
P PSR002 Psoriasis 63 2.212
261
HRN029 Hearing Loss, Noise-Induced 37 2.204
262
P ATX030 Ataxia-Telangiectasia 80 2.204
263
URM002 Uremia 47 2.204
264
SLP001 Sleeping Sickness 56 2.204
265
P ORT004 Orthostatic Intolerance 63 2.183
266
RBF001 Riboflavin Deficiency 49 2.183
267
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 2.183
268
VSC002 Vascular Dementia 60 2.183
269
LYM133 Lymphoma, Hodgkin, Classic 74 2.167
270
LYM143 Lymphoma, Non-Hodgkin, Familial 75 2.167
271
GTR002 Goiter 53 2.166
272
CRB090 Cerebral Hypoxia 42 2.166
273
c CNG223 Congenital Methemoglobinemia 39 2.157
274
VSC003 Visceral Leishmaniasis 55 2.134
275
P KDN017 Kidney Cancer 61 2.134
276
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 2.127
277
DSS032 Disease by Infectious Agent 55 2.127
278
P HYP098 Hypereosinophilic Syndrome 66 2.127
279
SCH014 Schistosomiasis 56 2.127
280
P PRP029 Porphyria 60 2.127
281
P TMP001 Temporal Lobe Epilepsy 49 2.120
282
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 2.098
283
P MYS005 Myositis 56 2.096
284
PLM010 Pulmonary Edema 55 2.096
285
GRN017 Granulocytopenia 42 2.096
286
LMB062 Limb Ischemia 55 2.086
287
P RHN004 Rhinitis 57 2.086
288
STN013 Stenotrophomonas Maltophilia Infection 26 2.062
289
INS001 Insulinoma 59 2.062
290
P ATS364 Autism 69 2.051
291
MLD001 Melioidosis 67 2.051
292
P ANT006 Antiphospholipid Syndrome 55 2.051
293
HMN002 Human Granulocytic Anaplasmosis 31 2.045
294
P FCL005 Focal Segmental Glomerulosclerosis 57 2.045
295
EHR002 Ehrlichiosis 39 2.045
296
OST017 Osteomyelitis 63 2.024
297
P RTN024 Retinoblastoma 73 2.019
298
P DMN002 Dementia 66 2.019
299
P BRS044 Breast Adenocarcinoma 58 2.003
300
RLP002 Relapsing-Remitting Multiple Sclerosis 56 2.003
301
MTC005 Mitochondrial Metabolism Disease 45 2.002
302
P MTH007 Methemoglobinemia 46 2.002
303
GST023 Gastric Ulcer 52 2.002
304
P LNG064 Lung Cancer Susceptibility 3 70 1.986
305
P RNL015 Renal Hypertension 45 1.986
306
MST005 Mastitis 53 1.986
307
SCR011 Scrapie 39 1.958
308
KDN013 Kidney Hypertrophy 34 1.958
309
ANG054 Angina Pectoris 66 1.954
310
PRP080 Peripheral Artery Disease 54 1.954
311
PNG002 Pain Agnosia 51 1.954
312
P SYS005 Systemic Scleroderma 74 1.954
313
NPH091 Nephrolithiasis, Calcium Oxalate 61 1.947
314
NRR001 Neuroretinitis 42 1.912
315
P AMY004 Amyloidosis 70 1.912
316
RTN023 Retinitis 46 1.912
317
P PLY019 Polyneuropathy 52 1.910
318
P PLY011 Polycystic Ovary Syndrome 57 1.906
319
TLR001 Tularemia 56 1.906
320
P RTN008 Retinitis Pigmentosa 80 1.865
321
P BRS047 Breast Cancer 98 1.865
322
P CND004 Candidiasis 58 1.865
323
P LCT001 Lactic Acidosis 51 1.865
324
ANT024 Anthrax Disease 58 1.865
325
VCC001 Vaccinia 47 1.865
326
BRK010 Burkitt Lymphoma 66 1.850
327
c ATS007 Autism Spectrum Disorder 72 1.850
328
LKS001 Leukostasis 41 1.850
329
CRV035 Cervical Cancer 73 1.822
330
ANT003 Antley-Bixler Syndrome 49 1.822
331
c SML038 Small Cell Cancer of the Lung 69 1.822
332
ACH005 Achalasia 55 1.822
333
CHL147 Chlamydia Pneumonia 47 1.822
334
P GLY013 Glycogen Storage Disease 60 1.822
335
ALC005 Alcoholic Pancreatitis 38 1.822
336
HMP009 Haemophilus Influenzae 41 1.822
337
SLC006 Silicosis 56 1.816
338
CNS004 Constipation 56 1.803
339
CRD223 Cardiac Arrhythmia 63 1.793
340
LST001 Listeriosis 59 1.793
341
ENT011 Enterocolitis 55 1.778
342
P PRS040 Prostate Cancer 95 1.778
343
ARG004 Argyria 26 1.778
344
P HRP006 Herpes Simplex 65 1.778
345
CNN003 Conn's Syndrome 79 1.778
346
CRT013 Carotid Stenosis 51 1.778
347
HLL004 Hellp Syndrome 53 1.778
348
P TXP001 Toxoplasmosis 60 1.778
349
OVR094 Ovarian Epithelial Cancer 39 1.778
350
TRY001 Trypanosomiasis 50 1.769
351
P DRM053 Dermatitis, Atopic 65 1.765
352
P GRV001 Graves' Disease 55 1.765
353
ALC006 Alcoholic Hepatitis 61 1.765
354
SVR004 Severe Combined Immunodeficiency 72 1.765
355
P EYD002 Eye Disease 57 1.765
356
c GRN065 Granulomatous Disease, Chronic, Autosomal Recessive, 5 23 1.738
357
CRN027 Corneal Neovascularization 47 1.734
358
c ACT134 Acute Liver Failure 59 1.733
359
c ATS307 Autosomal Recessive Cerebellar Ataxia 39 1.733
360
P TRM003 Tremor 48 1.733
361
P NPH012 Nephrotic Syndrome 60 1.733
362
PLP001 Pulpitis 48 1.733
363
P SLP005 Sleep Disorder 61 1.733
364
DPR016 Depression 65 1.733
365
CRT065 Cortisone Reductase Deficiency 1 25 1.723
366
FRN006 Frontotemporal Dementia 68 1.711
367
ANX010 Anxiety 70 1.711
368
XRD010 Xeroderma Pigmentosum, Variant Type 73 1.711
369
MYL069 Myeloma, Multiple 77 1.711
370
c VRL010 Viral Hepatitis 53 1.711
371
PLC002 Plica Syndrome 35 1.711
372
THY030 Thyroid Gland Disease 50 1.711
373
SYN007 Synovitis 55 1.711
374
PST028 Post-Traumatic Stress Disorder 59 1.711
375
PHN003 Phenylketonuria 76 1.685
377
CHR074 Choriocarcinoma 46 1.685
378
OST003 Osteonecrosis 61 1.685
379
NNT012 Neonatal Jaundice 53 1.685
380
P END044 Endometriosis 62 1.685
381
BLR008 Bilirubin Metabolic Disorder 57 1.664
382
P LYM118 Lymphoma 67 1.655
383
ACT084 Acute Stress Disorder 54 1.655
384
MCR013 Microphthalmia 60 1.655
385
PHR003 Pharyngitis 58 1.655
386
ALC007 Alcohol Dependence 66 1.636
387
MYL009 Myelodysplastic Syndrome 67 1.636
388
OCL069 Ocular Motor Apraxia 57 1.636
389
FML063 Familial Glucocorticoid Deficiency 58 1.636
390
P THR014 Thrombocytopenia 66 1.636
391
P MNC007 Monocytic Leukemia 47 1.636
392
P ESP024 Esophagitis 60 1.636
393
ATN005 Autonomic Dysfunction 46 1.636
394
P EPL164 Epilepsy 68 1.602
395
MLD018 Mild Cognitive Impairment 48 1.596
396
P HPT021 Hepatitis 69 1.596
397
DMY004 Demyelinating Disease 50 1.596
398
ART074 Aortic Dissection 53 1.585
399
P GLC113 Galactosemia I 66 1.585
400
ORL015 Oral Squamous Cell Carcinoma 43 1.585
401
PRM329 Premature Aging 36 1.585
402
P HMC002 Homocystinuria 53 1.585
403
PSD009 Pseudohermaphroditism 46 1.585
404
P THY032 Thyroiditis 57 1.585
405
P GRF003 Graft-Versus-Host Disease 71 1.585
406
P PYL005 Pyelonephritis 57 1.585
407
CCN002 Cocaine Abuse 49 1.585
408
P OVR082 Overgrowth Syndrome 49 1.532
409
PSR001 Psoriatic Arthritis 62 1.532
410
CRT004 Carotid Artery Thrombosis 39 1.532
411
GNT167 Genetic Obesity 30 1.532
412
P ANP001 Anaplastic Large Cell Lymphoma 61 1.532
413
CRH005 Crohn's Colitis 53 1.532
414
c ATM022 Autoimmune Myocarditis 36 1.532
415
LKC009 Leukocyte Adhesion Deficiency, Type I 70 1.532
416
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 1.532
417
HYP006 Hypertensive Heart Disease 49 1.532
418
DBT008 Diabetic Angiopathy 45 1.528
419
SPS057 Spasticity 42 1.475
420
ALL003 Allergic Rhinitis 67 1.475
421
c NTR047 Neutropenia, Severe Congenital, 1, Autosomal Dominant 37 1.475
422
NRM005 Neuromuscular Disease 63 1.475
423
RCK004 Rickets 68 1.475
424
KHN001 Kuhnt-Junius Degeneration 48 1.475
425
HYP026 Hypoglycemic Coma 37 1.475
426
LCH001 Leech Infestation 38 1.475
427
PRN019 Perinatal Necrotizing Enterocolitis 60 1.475
428
P OVR042 Ovarian Cancer 88 1.472
429
P OPN001 Open-Angle Glaucoma 55 1.472
430
MTH026 Methemoglobinemia Due to Deficiency of Methemoglobin Reductase 35 1.464
431
PLR008 Pleurisy 50 1.464
432
ORL011 Oral Cancer 60 1.464
433
CRD132 Cardiac Conduction Defect 60 1.416
434
P SCH015 Schizophrenia 74 1.416
435
URL001 Urolithiasis 46 1.416
436
NRL016 Neural Tube Defects 81 1.416
437
c DPH024 Diaphragmatic Hernia, Congenital 64 1.416
438
TRC022 Tricuspid Valve Insufficiency 47 1.416
439
MTR002 Mitral Valve Insufficiency 52 1.416
440
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.390
441
MRF001 Marfan Syndrome 76 1.390
442
P BND020 Bone Disease 59 1.390
443
MLT157 Multiple System Atrophy 1 69 1.388
444
ESP021 Esophageal Cancer 83 1.388
445
c GLC092 Glaucoma, Primary Open Angle 62 1.388
446
P MLN007 Male Infertility 56 1.388
447
PYL006 Pyloric Stenosis 48 1.388
448
SMT004 Smith-Lemli-Opitz Syndrome 70 1.352
449
c OPT051 Opitz Gbbb Syndrome, Type I 46 1.352
450
WLL001 Williams-Beuren Syndrome 61 1.352
451
P MGL010 Megalencephalic Leukoencephalopathy with Subcortical Cysts 2a 40 1.352
452
c RTN143 Retinitis Pigmentosa 47 41 1.352
453
c BRN108 Branchiootic Syndrome 1 62 1.352
454
c RTN140 Retinitis Pigmentosa 67 32 1.352
455
CTN007 Cutaneous Leishmaniasis 62 1.352
456
DGN001 Degenerative Disc Disease 49 1.352
457
ACQ007 Acquired Immunodeficiency Syndrome 59 1.352
458
P ACN011 Acne 57 1.352
459
P UVT001 Uveitis 57 1.352
460
P HYP061 Hypertrophic Cardiomyopathy 69 1.352
461
TXC004 Toxic Diffuse Goiter 23 1.352
462
P MTR012 Mitral Valve Disease 57 1.352
463
P BNG032 Benign Mesothelioma 53 1.352
464
MST020 Mast Cell Activation Syndrome 28 1.352
465
HDN002 Head Injury 44 1.352
466
P CHR345 Chronic Pain 50 1.352
467
P GLM040 Glioma Susceptibility 1 71 1.344
468
P BRB001 Beriberi 44 1.344
469
P MTR014 Motor Neuron Disease 65 1.344
470
P HYP009 Hypertrophic Pyloric Stenosis 41 1.344
471
c SVR005 Severe Pre-Eclampsia 50 1.344
472
BRN056 Bronchopulmonary Dysplasia 56 1.344
473
P AGG001 Aggressive Periodontitis 55 1.308
474
OBS082 Obstructive Nephropathy 41 1.298
475
MLG169 Malignant Astrocytoma 57 1.298
476
LYM021 Lymphadenitis 56 1.298
477
MLG163 Malignant Tumor of Penis 29 1.284
478
P SZR006 Seizure Disorder 70 1.284
479
P STR035 Streptococcal Group a Invasive Disease 24 1.284
480
MTB004 Metabolic Acidosis 48 1.284
481
ACT098 Acute Erythroid Leukemia 55 1.284
482
MYL005 Myelofibrosis 71 1.284
483
RFS006 Refsum Disease, Classic 63 1.284
484
GLB001 Gilbert Syndrome 53 1.284
485
P CRC039 Coarctation of Aorta 46 1.284
486
P CHR285 Chronic Myelomonocytic Leukemia 60 1.284
487
PRP007 Priapism 47 1.284
488
GST040 Gastric Adenocarcinoma 67 1.284
489
PPT005 Peptic Ulcer Disease 58 1.284
490
CLN015 Colon Adenocarcinoma 65 1.284
491
IRN001 Iron Deficiency Anemia 58 1.284
492
HMN014 Human Immunodeficiency Virus Infectious Disease 54 1.284
493
P INT068 Intestinal Disease 53 1.284
494
P TRT010 Teratoma 51 1.284
495
BRN002 Bronchiolitis 57 1.284
496
PNL012 Penile Cancer 57 1.284
497
KLD004 Keloid Disorder 39 1.284
498
P MYT002 Myotonic Dystrophy 51 1.284
499
c JVN010 Juvenile Rheumatoid Arthritis 66 1.284
500
c RNG019 Ring Chromosome 3 19 1.284
501
SHR103 Short Stature, Developmental Delay, and Congenital Heart Defects 29 1.284
502
RTN017 Retinal Detachment 60 1.251
503
P SRC025 Sarcoidosis 1 71 1.251
504
CHL065 Cholangiocarcinoma 58 1.251
505
GT001 Gout 64 1.251
506
HGH043 High Grade Glioma 45 1.251
507
INT079 Intrahepatic Cholangiocarcinoma 51 1.251
508
DBT007 Diabetic Cataract 36 1.251
509
P VTR007 Vitreoretinopathy 46 1.215
510
CRT084 Creatinine Clearance Quantitative Trait Locus 25 1.215
511
WTH001 Withdrawal Disorder 48 1.215
512
PHG002 Phagocyte Bactericidal Dysfunction 34 1.215
513
P ECT006 Ectodermal Dysplasia 63 1.215
514
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 1.210
515
c CHR711 Chronic Asthma 41 1.210
516
ANT042 Antley-Bixler Syndrome with Genital Anomalies and Disordered Steroidogenesis 35 1.210
517
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 1.210
518
c THY109 Thyroid Cancer, Nonmedullary, 1 55 1.210
519
TST044 Testicular Torsion 45 1.210
520
ACT003 Acute Kidney Tubular Necrosis 46 1.210
521
HRT012 Heart Valve Disease 53 1.210
522
EXT034 Extrinsic Allergic Alveolitis 57 1.210
523
EPD006 Epidermolysis Bullosa Acquisita 48 1.210
524
P DDN001 Duodenal Ulcer 53 1.210
525
TTN003 Tetanus 65 1.210
526
ART004 Aortic Atherosclerosis 47 1.210
527
MCL006 Macular Retinal Edema 57 1.210
528
P EPD016 Epidermolysis Bullosa 53 1.210
529
SGN002 Signet Ring Cell Adenocarcinoma 46 1.210
530
PNM001 Pneumocystosis 61 1.210
531
PPT001 Peptic Esophagitis 52 1.210
532
P MNN013 Meningitis 65 1.210
533
SPL018 Splenomegaly 49 1.210
534
KPS004 Kaposi Sarcoma 77 1.202
535
c ACT068 Acute Cystitis 61 1.202
536
P THL005 Thalassemia 56 1.151
537
HRW001 Hair Whorl 35 1.151
538
P CYS018 Cystitis 59 1.151
539
OVR063 Overnutrition 42 1.151
540
c ATM011 Autoimmune Hepatitis 63 1.151
541
P RSP003 Respiratory Failure 74 1.151
542
STR077 Streptococcal Toxic-Shock Syndrome 35 1.128
543
PNM013 Pneumococcal Meningitis 43 1.128
544
SPN119 Spondylarthropathy 38 1.128
545
ADN027 Adenomyosis 57 1.128
546
ASP026 Asplenia, Isolated Congenital 43 1.128
547
P FRG001 Fragile X Syndrome 70 1.128
548
XNT003 Xanthomatosis 49 1.128
549
P LKM071 Leukemia, Chronic Lymphocytic 75 1.128
550
c MST023 Mesothelioma, Malignant 56 1.128
551
c FNC027 Fanconi Anemia, Complementation Group a 81 1.128
552
CMP034 Complete Androgen Insensitivity Syndrome 55 1.128
553
ILC002 Ileocolitis 43 1.128
554
RHM028 Rheumatic Heart Disease 56 1.128
555
CRB011 Cerebrotendinous Xanthomatosis 65 1.128
556
P PRP003 Porphyria Cutanea Tarda 66 1.128
557
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 1.128
559
THR100 Thrombocytopenic Purpura, Autoimmune 61 1.128
560
URT049 Urate Oxidase, Pseudogene 24 1.128
561
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 1.128
562
BRN147 Brain Inflammatory Disease 7 1.128
563
P CHL066 Cholangitis 52 1.128
564
P SBR004 Seborrheic Dermatitis 44 1.128
565
CRV038 Cervical Squamous Cell Carcinoma 58 1.128
566
P ESN008 Eosinophilic Pneumonia 50 1.128
567
P DNG005 Dengue Virus 56 1.128
568
P HMN010 Hemangioma 62 1.128
569
P GCH001 Gaucher's Disease 70 1.128
570
MCS002 Mucositis 56 1.128
571
VSM001 Vasomotor Rhinitis 38 1.128
572
PRP030 Purpura 54 1.128
573
RHM001 Rheumatic Fever 59 1.128
574
P DRR001 Diarrhea 55 1.128
575
NCR007 Necrotizing Fasciitis 49 1.128
576
PLM035 Pulmonary Eosinophilia 49 1.128
577
FSC004 Fasciitis 49 1.128
578
TRC096 Trichothiodystrophy 55 1.128
579
CRB086 Cerebral Aneurysms 40 1.128
580
P CRB059 Cerebellar Degeneration 36 1.128
581
CYT018 Cytochrome P450 2d6 Variant 26 1.128
582
CRT072 Creutzfeldt-Jakob Disease 68 1.105
583
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 57 1.105
584
P DMY001 Demyelinating Polyneuropathy 41 1.105
585
PLM033 Pulmonary Embolism 58 1.105
586
SBC016 Subacute Delirium 43 1.105
587
PRQ002 Paraquat Poisoning 28 1.097
588
GLM044 Glomerular Disease 35 1.097
589
VLV047 Volvulus of Midgut 52 1.097
590
PLT004 Platelet Glycoprotein Iv Deficiency 56 1.097
591
P EXN002 Exanthem 58 1.097
592
P LKM062 Leukemia, Acute Lymphoblastic 69 1.097
593
DWN001 Down Syndrome 70 1.097
594
CRT020 Cortisone Reductase Deficiency 34 1.097
595
LMY002 Leiomyoma 51 1.097
596
c ACT075 Acute Myocardial Infarction 56 1.097
597
AMB001 Amebiasis 57 1.097
598
DST006 Diastolic Heart Failure 45 1.097
599
HVY002 Heavy Metal Poisoning 22 1.097
600
P LPR021 Leprosy 3 71 1.041
601
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 1.041
602
P APL001 Aplastic Anemia 73 1.041
603
P ADL017 Adult T-Cell Leukemia 56 1.041
604
c SVR003 Severe Congenital Neutropenia 59 1.041
605
c HYP602 Hyperoxaluria, Primary, Type Ii 49 1.041
606
VRC005 Varicose Veins 60 1.041
607
ACT149 Acetaminophen Metabolism 35 1.041
608
IGG001 Iga Glomerulonephritis 50 1.041
609
SPN035 Spindle Cell Sarcoma 54 1.041
610
P MMB011 Membranous Nephropathy 50 1.041
612
DPH001 Diphtheria 59 1.041
613
SRC014 Sarcoma 65 1.041
614
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 1.041
615
P PRM002 Primary Hyperoxaluria 65 1.041
616
GST045 Gastroenteritis 58 1.041
617
P OBS001 Obstructive Jaundice 48 1.041
618
c FML021 Familial Hypercholesterolemia 72 1.041
619
HNS001 Hansen's Disease 32 1.041
620
c LKM005 Leukemia, T-Cell, Chronic 34 1.041
621
P MRC003 Mercury Poisoning 49 1.041
622
LYS003 Lysinuric Protein Intolerance 57 1.035
623
GLY111 Glycogen Storage Disease Due to Glucose-6-Phosphatase Deficiency Type Ib 29 1.035
624
CYN002 Cyanosis, Transient Neonatal 43 1.035
625
OST006 Osteoblastoma 38 1.035
626
P FTL001 Fetal Alcohol Syndrome 55 1.035
627
c SCN036 Secondary Progressive Multiple Sclerosis 55 1.035
628
CHR288 Chronic Recurrent Multifocal Osteomyelitis 60 1.035
629
P CRB048 Cerebral Cavernous Malformations 63 1.035
630
c PRG020 Paragangliomas 3 39 1.035
631
HYP114 Hypertensive Nephropathy 36 1.035
632
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 1.035
633
P MDL005 Medulloblastoma 75 1.035
634
OCL052 Ocular Dominance 40 1.035
635
PRX001 Peroxisomal Disease 46 1.035
636
EXT007 Extracutaneous Mastocytoma 38 1.035
637
CRN030 Coronary Stenosis 50 1.035
638
c TRN047 Transient Congenital Hypothyroidism 22 1.035
639
MST004 Mast Cell Neoplasm 42 1.035
640
INT002 Intermittent Claudication 61 1.035
641
MLG079 Malignant Pleural Mesothelioma 42 1.035
642
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 1.035
643
CVR010 Cavernous Malformation 30 1.035
644
AMN006 Aminoaciduria 37 1.035
645
P TRM004 Trimethylaminuria 45 0.981
646
c OPT053 Optic Atrophy 1 62 0.981
647
c MJR022 Major Affective Disorder 8 38 0.981
648
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.981
649
P MJR001 Major Depressive Disorder 68 0.981
650
c MJR024 Major Affective Disorder 9 41 0.981
651
CLR109 Colorectal Adenocarcinoma 50 0.981
652
P PLM034 Pulmonary Emphysema 58 0.981
653
P BPL003 Bipolar Disorder 56 0.981
654
MNT002 Mental Depression 57 0.981
655
CLR030 Clear Cell Renal Cell Carcinoma 54 0.981
656
INT060 Intestinal Atresia 41 0.981
657
HRP004 Herpes Zoster 61 0.981
658
P ENC004 Encephalitis 61 0.981
659
CND006 Candida Glabrata 30 0.981
660
PRT058 Pure Autonomic Failure 58 0.981
661
P PLY180 Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy 1 56 0.925
662
PLY100 Polyploidy 36 0.925
663
FBR032 Fibromuscular Dysplasia 48 0.925
664
CHR100 Chronic Ulcer of Skin 57 0.925
666
BTN004 Biotin Deficiency 45 0.925
667
THY121 Thyroid Gland Anaplastic Carcinoma 67 0.925
668
TRD006 Tardive Dyskinesia 53 0.925
669
EPT021 Epithelial Recurrent Erosion Dystrophy 46 0.925
670
c SPN291 Spinocerebellar Ataxia 7 53 0.925
671
TNG009 Tongue Squamous Cell Carcinoma 43 0.925
672
PLM014 Pleomorphic Adenoma 51 0.925
673
SYS071 Systemic Autoimmune Disease 35 0.925
674
ACY011 Acyl-Coa Dehydrogenase Deficiency 30 0.925
675
P VNT002 Ventricular Septal Defect 58 0.925
676
c ACT076 Acute Myocarditis 47 0.925
677
ANG020 Angiosarcoma 64 0.925
678
DNG002 Dengue Hemorrhagic Fever 60 0.925
679
PRM236 Primary Biliary Cholangitis 60 0.925
680
CRV040 Cervix Carcinoma 50 0.925
681
CRY003 Cryptosporidiosis 56 0.925
682
KRT009 Keratosis 53 0.925
683
HYD002 Hydronephrosis 58 0.925
684
P TCD001 Tic Disorder 49 0.925
685
MDD011 Mood Disorder 62 0.925
686
DRM006 Dermatitis 62 0.925
687
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.925
688
P DSR090 Disorder of Sexual Development 44 0.925
689
P TRC031 Trichorhinophalangeal Syndrome 38 0.925
690
c NNS007 Nonsyndromic Deafness 33 0.925
691
CRB087 Cerebral Arteriosclerosis 17 0.925
692
CTN027 Cutaneous Mastocytoma 26 0.925
693
MYC017 Mycobacterium Kansasii 36 0.925
694
DXR001 Doxorubicin Induced Cardiomyopathy 32 0.925
695
ADR022 Adrenomyeloneuropathy 39 0.918
696
ADR007 Adrenoleukodystrophy 73 0.918
697
LMY014 Leiomyoma, Uterine 56 0.918
698
SCK003 Sickle Cell Anemia 74 0.918
699
c PRD040 Periodontitis, Chronic 52 0.918
700
c PYL018 Pyloric Stenosis, Infantile Hypertrophic, 1 35 0.918
701
c TBR025 Tuberous Sclerosis 1 84 0.918
702
ADR041 Adrenal Cortical Adenoma 49 0.918
703
P HML001 Hemolytic-Uremic Syndrome 52 0.918
704
P RHB003 Rhabdomyosarcoma 66 0.918
705
VRL011 Viral Infectious Disease 61 0.918
706
c BCT013 Bacterial Pneumonia 48 0.918
707
P GLL022 Guillain-Barre Syndrome 60 0.918
708
SNS003 Sensory Peripheral Neuropathy 52 0.918
709
P TBR001 Tuberous Sclerosis 69 0.918
710
GST033 Gestational Diabetes 61 0.918
711
P MCR010 Microcephaly 60 0.918
712
BRN024 Bronchitis 67 0.918
713
PLS007 Plasmodium Falciparum Malaria 52 0.918
714
MGC001 Megacolon 48 0.918
715
P DYS021 Dysautonomia 38 0.918
716
OST115 Osteonecrosis of the Jaw 41 0.850
717
P HYP605 Hyperphenylalaninemia, Bh4-Deficient, B 44 0.850
718
ADR016 Adrenal Cortical Carcinoma 62 0.850
719
HYP025 Hyperphosphatemia 48 0.850
720
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.850
721
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.850
722
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.850
723
P SPP010 Suppressor of Tumorigenicity 3 51 0.850
724
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.850
725
P ALP008 Alopecia 54 0.850
726
c PRG106 Progressive Muscular Dystrophy 32 0.850
727
ADR004 Adrenal Cortical Adenocarcinoma 38 0.850
728
PLM001 Pulmonary Tuberculosis 69 0.850
729
P INT070 Intestinal Obstruction 57 0.850
730
P SNS001 Sensorineural Hearing Loss 59 0.850
731
P HMP002 Hemophagocytic Lymphohistiocytosis 61 0.850
732
c ATM104 Autoimmune Vasculitis 37 0.850
733
PLM012 Pulmonary Sarcoidosis 53 0.850
734
CNG017 Congenital Nonspherocytic Hemolytic Anemia 33 0.850
735
KRT002 Keratomalacia 55 0.850
736
LMY003 Leiomyomatosis 44 0.850
737
INT020 Intravenous Leiomyomatosis 36 0.850
738
INT066 Interstitial Lung Disease 60 0.850
739
KRT008 Keratopathy 46 0.850
740
HYP080 Hypogonadism 50 0.850
741
WLL004 Wallerian Degeneration 38 0.850
742
CHR178 Chromosomal Triplication 34 0.850
743
LYM019 Lymphosarcoma 46 0.850
744
MGL012 Megaloblastic Anemia Due to Dihydrofolate Reductase Deficiency 31 0.793
745
CRT066 Cortisone Reductase Deficiency 2 23 0.793
746
PDT035 Pediatric Systemic Lupus Erythematosus 47 0.781
748
P AVS003 Avascular Necrosis 41 0.781
749
c ART115 Aortic Valve Disease 1 74 0.781
750
RST011 Restrictive Dermopathy, Lethal 51 0.781
751
OBS002 Obsessive-Compulsive Disorder 68 0.781
752
HYP457 Hypertrophic Scars 42 0.781
753
FTL006 Fetal Alcohol Spectrum Disorder 43 0.781
754
c ATM099 Autoimmune Uveitis 45 0.781
755
c ACT249 Acute Asthma 40 0.781
756
ECT108 Ectodermal Dysplasia and Immunodeficiency 1 38 0.781
757
GRG001 Greig Cephalopolysyndactyly Syndrome 64 0.781
758
PNB004 Panbronchiolitis, Diffuse 34 0.781
759
KWS002 Kawasaki Disease 65 0.781
760
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.781
761
IMM222 Immunodeficiency 67 41 0.781
762
GYN001 Gynecomastia 47 0.781
763
MTC004 Mitochondrial Encephalomyopathy 42 0.781
764
P ATR005 Atrophic Gastritis 50 0.781
765
P ALK015 Alk-Positive Anaplastic Large Cell Lymphoma 39 0.781
766
HRT011 Heart Septal Defect 49 0.781
767
OVR059 Ovary Adenocarcinoma 49 0.781
768
P ART023 Arthropathy 61 0.781
769
STR103 Streptococcus Pneumonia 47 0.781
770
BLR002 Bile Reflux 38 0.781
771
NRX001 Neuroaxonal Dystrophy 38 0.781
772
PPL022 Papilloma 53 0.781
773
DRG002 Drug-Induced Hepatitis 42 0.781
774
HYP068 Hyperostosis 47 0.781
775
CCC001 Coccidioidomycosis 58 0.781
776
c MLG069 Malignant Hypertension 46 0.781
777
CDQ001 Cauda Equina Syndrome 37 0.781
778
INF021 Infant Gynecomastia 30 0.781
779
EMB004 Embryonal Carcinoma 56 0.781
780
GNG012 Gingival Overgrowth 49 0.781
781
c CNT035 Central Nervous System Disease 54 0.781
782
BNN003 Bone Inflammation Disease 48 0.781
783
SPH001 Sapho Syndrome 47 0.781
784
P NRV007 Nervous System Disease 67 0.781
785
NPH018 Nephrogenic Systemic Fibrosis 49 0.781
786
c HMC039 Hemochromatosis, Type 1 73 0.776
787
ALD013 Aldosterone-Producing Adenoma 36 0.776
788
DHY002 Dihydropyrimidine Dehydrogenase Deficiency 57 0.776
789
HMR023 Hemorrhagic Cystitis 43 0.776
790
BCT021 Bacterial Sepsis 43 0.776
791
P URN019 Urinary Tract Infection 49 0.776
792
SXL003 Sexual Disorder 49 0.776
793
c 2HY001 2-Hydroxyglutaric Aciduria 38 0.776
794
P CHN012 Chondrosarcoma 57 0.776
795
MSN001 Mesangial Proliferative Glomerulonephritis 44 0.776
796
CRC021 Carcinosarcoma 64 0.776
797
P MVM001 Movement Disease 61 0.776
798
P MTC133 Mitochondrial Myopathy 50 0.776
799
ADG002 Audiogenic Seizures 25 0.776
800
P PLY018 Polycythemia 56 0.776
801
P VNS003 Venous Insufficiency 55 0.776
802
DYS015 Dysentery 50 0.776
803
LWC001 Low Compliance Bladder 45 0.776
804
ORC001 Orchitis 44 0.776
805
CCC002 Coccidiosis 50 0.776
806
MYL031 Myeloproliferative Neoplasm 66 0.776
807
JPN002 Japanese Encephalitis 61 0.776
808
MNN009 Meningoencephalitis 48 0.776
809
URN010 Urinary Tract Obstruction 55 0.776
810
PLC008 Placenta Disease 49 0.776
811
CRT016 Carotid Artery Disease 52 0.776
812
P OST001 Osteopetrosis 71 0.776
813
P RCT021 Rectum Cancer 54 0.776
814
HYP141 Hyperphenylalaninemia 42 0.776
815
c ACT135 Acute Graft Versus Host Disease 51 0.776
816
c RNG021 Ring Chromosome 5 20 0.776
817
P FML187 Familial Hypertension 34 0.776
818
c BCT007 Bacterial Meningitis 55 0.694
819
DSC009 Discoid Lupus Erythematosus 43 0.694
820
ACT228 Acute Radiation Syndrome 30 0.694
821
HMZ003 Homozygous Familial Hypercholesterolemia 60 0.694
822
c GLL024 Gallbladder Disease 1 52 0.694
823
P D2H002 D-2-Hydroxyglutaric Aciduria 1 52 0.694
824
c LKM070 Leukemia, Acute Monocytic 56 0.694
825
c MGR028 Migraine with or Without Aura 1 64 0.694
826
DGL002 D-Glyceric Aciduria 41 0.694
827
c BTT014 Beta-Thalassemia 72 0.694
828
ATR057 Atrioventricular Block 54 0.694
829
CVD001 Covid-19 57 0.694
830
ILT001 Ileitis 48 0.694
831
APP015 Apparent Mineralocorticoid Excess 57 0.694
832
c THY056 Thyroid Dyshormonogenesis 3 31 0.694
833
IGR001 Ige Responsiveness, Atopic 59 0.694
834
AGN004 Aganglionosis, Total Intestinal 23 0.694
835
HMC041 Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity 48 0.694
836
PSD021 Pseudovaginal Perineoscrotal Hypospadias 42 0.694
837
INT051 Intussusception 52 0.694
838
GST071 Gastrointestinal Carcinoma 46 0.694
839
P HRD008 Hereditary Hemorrhagic Telangiectasia 65 0.694
840
P ZLL001 Zellweger Syndrome 65 0.694
841
PRS042 Prostate Disease 42 0.694
842
INT007 Intermediate Coronary Syndrome 54 0.694
843
SKN019 Skin Melanoma 71 0.694
844
P RBL001 Rubella 58 0.694
845
P MLG056 Malignant Hyperthermia 66 0.694
846
HGH041 High-Grade Astrocytoma 36 0.694
847
TRT001 Teratocarcinoma 42 0.694
848
PLC005 Placental Insufficiency 56 0.694
849
FLL031 Follicular Adenoma 40 0.694
850
P KRT007 Keratoconus 50 0.694
851
c FML297 Familial Thyroid Dyshormonogenesis 47 0.694
852
ALC010 Alcoholic Cardiomyopathy 42 0.694
853
LYM009 Lymphocytic Choriomeningitis 46 0.694
854
VRC001 Varicocele 48 0.694
855
PYL002 Pylorospasm 23 0.694
856
TST015 Testicular Disease 42 0.694
857
GLS001 Gliosarcoma 64 0.694
858
RBS001 Rabies 58 0.694
859
IMM001 Immune-Complex Glomerulonephritis 36 0.694
860
EXC002 Exocrine Pancreatic Insufficiency 42 0.694
861
ENT004 Enthesopathy 51 0.694
862
DYS032 Dystrophinopathies 47 0.694
863
7Q1002 7q11.23 Duplication Syndrome 33 0.694
864
PRM209 Primary Trimethylaminuria 19 0.694
865
ACT200 Acute Monoblastic Leukemia 41 0.694
866
MYC005 Myocardial Stunning 46 0.694
867
c RNG008 Ring Chromosome 13 30 0.694
868
G6P001 G6pc3 Deficiency 23 0.694
869
P MTC069 Mitochondrial Disorders 57 0.694
870
PTT037 Pituitary Tumors 44 0.694
871
MYC019 Mycobacterium Marinum 29 0.694
872
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 0.649
873
ANT039 Antisynthetase Syndrome 55 0.649
874
MCK005 Mckusick-Kaufman Syndrome 61 0.601
875
HYP625 Hyperandrogenism Due to Cortisone Reductase Deficiency 15 0.601
876
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.601
877
BNG077 Benign Idiopathic Neonatal Seizures 23 0.601
878
P RTT002 Rett Syndrome 79 0.601
879
MCL009 Mcleod Syndrome 46 0.601
880
P WSK001 Wiskott-Aldrich Syndrome 72 0.601
881
SDD001 Sudden Infant Death Syndrome 60 0.601
882
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 62 0.601
883
MYC072 Myoclonic Epilepsy Associated with Ragged-Red Fibers 45 0.601
884
FLT006 Floating-Harbor Syndrome 52 0.601
885
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.601
886
OTT002 Otitis Media 71 0.601
887
P HYP769 Hyperlysinemia, Type I 42 0.601
888
P MLT008 Multinodular Goiter 42 0.601
889
GLT039 Glutathione Peroxidase Deficiency 33 0.601
890
DFF005 Diffuse Large B-Cell Lymphoma 54 0.601
891
P STR022 Stargardt Disease 61 0.601
892
P ERY036 Erythema Nodosum 49 0.601
893
SNT005 Sinoatrial Node Disease 47 0.601
894
CNT105 Central Core Disease of Muscle 59 0.601
895
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.601
896
c PRT132 Protoporphyria, Erythropoietic, 1 61 0.601
897
TRN021 Transaldolase Deficiency 43 0.601
898
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.601
899
LPT014 Leptin Deficiency or Dysfunction 78 0.601
900
CHR515 Chronic Atrial and Intestinal Dysrhythmia 43 0.601
901
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.601
902
HMC033 Homocystinuria-Megaloblastic Anemia, Cblg Complementation Type 34 0.601
903
CHD001 Chediak-Higashi Syndrome 67 0.601
904
HYP784 Hypogonadism, Male 43 0.601
905
c WLM013 Wilms Tumor 1 66 0.601
906
PLY001 Polycythemia Vera 69 0.601
907
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.601
908
P PTN014 Patent Ductus Arteriosus 1 59 0.601
909
OLG020 Oligoarticular Juvenile Idiopathic Arthritis 45 0.601
910
c PRM340 Primary Adrenal Insufficiency 38 0.601
911
ANG046 Angioimmunoblastic T-Cell Lymphoma 51 0.601
912
c HPT003 Hepatitis a 63 0.601
913
OCC016 Occupational Asthma 33 0.601
914
c ACT073 Acute Leukemia 58 0.601
915
XLN170 X-Linked Mendelian Susceptibility to Mycobacterial Diseases 21 0.601
916
FSC002 Fascioliasis 44 0.601
917
HPT009 Hepatopulmonary Syndrome 48 0.601
918
P DYS154 Dystonia 64 0.601
919
NTR005 Nutritional Deficiency Disease 61 0.601
920
P NRC002 Narcolepsy 56 0.601
921
P LCH002 Lichen Planus 54 0.601
922
INT040 Intrinsic Asthma 36 0.601
923
CHR066 Chronic Fatigue Syndrome 60 0.601
924
PRD003 Periodontosis 25 0.601
925
SVR001 Severe Acute Respiratory Syndrome 67 0.601
926
FDL002 Food Allergy 47 0.601
927
TRC003 Trichomoniasis 53 0.601
928
CLL003 Cellulitis 53 0.601
929
APP008 Appendicitis 62 0.601
930
LYM027 Lymphopenia 56 0.601
931
PYR009 Pyridoxine Deficiency Anemia 35 0.601
932
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.601
933
CMM005 Common Cold 56 0.601
934
ASP007 Aspiration Pneumonia 49 0.601
935
THY006 Thymus Lymphoma 27 0.601
936
OST011 Osteomalacia 52 0.601
937
BRN028 Brain Cancer 74 0.601
938
P SPN046 Spinal Muscular Atrophy 63 0.601
939
DNT012 Dental Caries 53 0.601
940
MYM001 Myoma 54 0.601
941
HRY003 Hairy Cell Leukemia 61 0.601
942
P HYP069 Hyperparathyroidism 62 0.601
943
NRT004 Neuritis 53 0.601
944
FNG017 Fungal Infectious Disease 54 0.601
945
P CRN037 Craniosynostosis 68 0.601
946
KDN001 Kidney Cortex Necrosis 33 0.601
947
URT001 Urethritis 53 0.601
948
GLN002 Glanders 38 0.601
949
FCL012 Facial Paralysis 49 0.601
950
P HYP040 Hypospadias 51 0.601
951
INT030 Intracranial Aneurysm 55 0.601
952
HYP043 Hyperandrogenism 48 0.601
953
c CNG027 Congenital Hemolytic Anemia 48 0.601
954
GST050 Gastrointestinal System Disease 55 0.601
955
P CTS001 Cutis Laxa 65 0.601
956