Search results for NADPH

639 hits were found for NADPH

# Family MCID Name MIFTS Score
1
MTH072 Methemoglobin Reductase Deficiency 16 2.914
2
P CHR012 Chronic Granulomatous Disease 67 0.389
3
P VSC007 Vascular Disease 63 0.235
4
HYP066 Hyperglycemia 61 0.199
5
c MCR113 Microvascular Complications of Diabetes 3 52 0.197
6
c MCR120 Microvascular Complications of Diabetes 7 47 0.197
7
c MCR130 Microvascular Complications of Diabetes 6 41 0.197
8
c MCR133 Microvascular Complications of Diabetes 4 41 0.197
9
ISC004 Ischemia 58 0.179
10
ATH013 Atherosclerosis Susceptibility 65 0.177
11
HYP266 Hypoxia 57 0.168
12
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.154
13
P PLM037 Pulmonary Hypertension 67 0.150
14
P MCR115 Microvascular Complications of Diabetes 5 66 0.144
15
CRB004 Cerebral Artery Occlusion 45 0.139
16
PRT037 Pertussis 65 0.134
17
BRN071 Brain Injury 49 0.128
18
P CLR023 Colorectal Cancer 99 0.122
19
TRM010 Traumatic Brain Injury 51 0.122
20
P SLP006 Sleep Apnea 69 0.119
21
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.119
22
P NRB001 Neuroblastoma 72 0.116
23
P PLM036 Pulmonary Fibrosis 65 0.113
24
P ALZ034 Alzheimer Disease 88 0.109
25
P LVR013 Liver Disease 68 0.109
26
c PRC016 Pre-Eclampsia 63 0.106
27
ATM095 Autoimmune Disease 62 0.106
28
IMP005 Impotence 52 0.106
29
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.102
30
P HRT032 Heart Disease 75 0.102
31
P HNT016 Huntington Disease 72 0.102
32
CNG034 Congestive Heart Failure 69 0.102
33
BCT022 Bacterial Infectious Disease 56 0.102
34
AGN016 Aging 56 0.102
35
P LTR001 Lateral Sclerosis 54 0.102
36
P HYP086 Hypothyroidism 69 0.098
37
LNG099 Lung Disease 60 0.098
38
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.095
39
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.095
40
P ADN016 Adenocarcinoma 64 0.095
41
SPN186 Spinal Cord Injury 60 0.095
42
RNL077 Renal Fibrosis 47 0.095
43
CYT002 Cytokine Deficiency 42 0.095
44
OST012 Osteoarthritis 78 0.091
45
GLB015 Glioblastoma Multiforme 75 0.091
46
c HYP836 Hypercholesterolemia, Familial, 1 73 0.091
47
P KDN018 Kidney Disease 72 0.091
48
BRR014 Barrett Esophagus 65 0.091
49
HMC014 Homocysteinemia 53 0.091
50
ART140 Arteries, Anomalies of 52 0.091
51
47X002 47,xyy 49 0.091
52
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.091
53
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.086
54
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.086
55
CRB039 Cerebrovascular Disease 67 0.086
56
LPP008 Lipoprotein Quantitative Trait Locus 62 0.086
57
FTT001 Fatty Liver Disease 61 0.086
58
P MYL006 Myeloid Leukemia 60 0.086
59
GRN051 Granulomatous Disease, Chronic, X-Linked 57 0.086
60
P INF037 Inflammatory Bowel Disease 54 0.086
61
NNL006 Non-Alcoholic Steatohepatitis 54 0.086
62
HLX001 Helix Syndrome 47 0.086
63
ANX004 Anoxia 40 0.086
64
ALL014 Allergic Encephalomyelitis 38 0.086
65
c LKM061 Leukemia, Acute Myeloid 84 0.082
66
ALL026 Allergic Hypersensitivity Disease 62 0.082
67
c SCL052 Scleroderma, Familial Progressive 61 0.082
68
BRN004 Brain Edema 56 0.082
69
END086 End Stage Renal Disease 51 0.082
70
RTN020 Retinal Vascular Disease 46 0.082
71
P HPT023 Hepatocellular Carcinoma 100 0.077
72
c ATR087 Atrial Standstill 1 75 0.077
73
c CHR684 Chronic Kidney Disease 70 0.077
74
CHL014 Cholera 59 0.077
75
P SCK005 Sickle Cell Disease 50 0.077
76
P GRN048 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative 48 0.077
77
PPL052 Papillomatosis, Confluent and Reticulated 33 0.077
78
PST092 Posttransplant Acute Limbic Encephalitis 29 0.077
79
P BRS047 Breast Cancer 97 0.072
80
c HYP595 Hypertension, Essential 84 0.072
81
P PNC035 Pancreatic Cancer 84 0.072
82
CYS001 Cystic Fibrosis 81 0.072
83
STR067 Stroke, Ischemic 81 0.072
84
P ASP006 Aspergillosis 69 0.072
85
P MSC005 Muscular Dystrophy 66 0.072
86
LPD008 Lipid Metabolism Disorder 62 0.072
87
c ACT027 Acute Pancreatitis 60 0.072
88
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.072
89
P CTR002 Cataract 60 0.072
90
STT001 Status Epilepticus 60 0.072
91
THY029 Thyroid Carcinoma 59 0.072
92
ADN018 Adenoma 59 0.072
93
HLC007 Helicobacter Pylori Infection 59 0.072
94
c GRN049 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I 46 0.072
95
48X005 48,xyyy 39 0.072
96
PLY150 Polykaryocytosis Inducer 31 0.072
98
P PRK057 Parkinson Disease, Late-Onset 78 0.067
99
P MYC007 Myocardial Infarction 70 0.067
100
ART016 Aortic Aneurysm 69 0.067
101
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.067
102
c CNG006 Congenital Hypothyroidism 64 0.067
103
SKN016 Skin Disease 63 0.067
104
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.067
105
HYP014 Hyperuricemia 52 0.067
106
P GST053 Gastric Cancer 83 0.061
107
P RHM011 Rheumatoid Arthritis 80 0.061
108
IMM167 Immune Deficiency Disease 78 0.061
109
P OST002 Osteoporosis 74 0.061
110
c HPT073 Hepatitis C Virus 72 0.061
111
P PHC003 Pheochromocytoma 71 0.061
112
c EXD008 Exudative Vitreoretinopathy 1 71 0.061
113
PRP027 Peripheral Vascular Disease 71 0.061
114
c MCR129 Microvascular Complications of Diabetes 1 66 0.061
115
CHG001 Chagas Disease 66 0.061
116
P HRS035 Hirschsprung Disease 1 65 0.061
117
CLT003 Colitis 62 0.061
118
CHL068 Cholestasis 61 0.061
119
P ALC033 Alcohol Use Disorder 58 0.061
120
P PRN023 Prion Disease 57 0.061
121
P CRD246 Cardiovascular System Disease 57 0.061
122
P FBR017 Fibrosarcoma 56 0.061
123
ALL006 Allergic Asthma 56 0.061
124
P GST044 Gastritis 56 0.061
125
NPH009 Nephrolithiasis 55 0.061
126
P ART021 Arteriosclerosis 54 0.061
127
BNR002 Bone Resorption Disease 48 0.061
128
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.061
129
ADR040 Adrenal Gland Pheochromocytoma 46 0.061
130
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.061
131
c MCR112 Microvascular Complications of Diabetes 2 41 0.061
132
c SYS001 Systemic Lupus Erythematosus 86 0.055
133
P BLD134 Bladder Cancer 79 0.055
134
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.055
135
ULC004 Ulcerative Colitis 73 0.055
136
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.055
137
P RTN024 Retinoblastoma 73 0.055
138
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.055
139
HMN044 Human Immunodeficiency Virus Type 1 71 0.055
140
LYM133 Lymphoma, Hodgkin, Classic 69 0.055
141
P LKM002 Leukemia 68 0.055
142
GST092 Gastroesophageal Reflux 67 0.055
143
ANG054 Angina Pectoris 66 0.055
144
P NSP012 Nasopharyngeal Carcinoma 66 0.055
145
PRT036 Peritonitis 64 0.055
146
LSH001 Leishmaniasis 63 0.055
147
ACT119 Acute Promyelocytic Leukemia 63 0.055
148
TRN015 Transient Cerebral Ischemia 63 0.055
149
TXC005 Toxic Shock Syndrome 62 0.055
150
LVR012 Liver Cirrhosis 62 0.055
151
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.055
152
P PNC044 Pancreatitis 61 0.055
153
P LPS004 Lupus Erythematosus 61 0.055
154
ANR040 Aneurysm 59 0.055
155
P NRP001 Neuropathy 56 0.055
156
P PLY019 Polyneuropathy 56 0.055
157
HPT022 Hepatoblastoma 56 0.055
158
HYP060 Hyperinsulinism 54 0.055
159
GLC003 Glucose Intolerance 54 0.055
160
DBT010 Diabetic Neuropathy 54 0.055
161
P RTN016 Retinal Degeneration 53 0.055
162
c FML008 Familial Retinoblastoma 53 0.055
163
P RTN018 Retinal Disease 53 0.055
164
P MSC003 Muscular Atrophy 52 0.055
165
RTN003 Retinal Ischemia 50 0.055
166
P ECL001 Eclampsia 50 0.055
167
c INV001 Invasive Aspergillosis 49 0.055
168
ATS010 Autosomal Recessive Disease 48 0.055
169
c PCH010 Pachyonychia Congenita 3 44 0.055
170
c GRN050 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type Ii 42 0.055
171
P KLZ004 Kala-Azar 1 41 0.055
172
CYT014 Cytochrome P450 Oxidoreductase Deficiency 32 0.055
173
P LNG032 Lung Cancer 98 0.047
174
P PRS040 Prostate Cancer 97 0.047
175
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.047
176
END057 Endometrial Cancer 74 0.047
177
P MLT020 Multiple Sclerosis 72 0.047
178
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.047
179
P MYP004 Myopathy 70 0.047
180
P MLN008 Melanoma 69 0.047
181
P LYM118 Lymphoma 68 0.047
182
P SYS005 Systemic Scleroderma 68 0.047
183
MLD001 Melioidosis 68 0.047
184
PNC129 Pancreatic Adenocarcinoma 68 0.047
185
BRK010 Burkitt Lymphoma 67 0.047
186
P SKN015 Skin Carcinoma 66 0.047
187
HYP056 Hypoglycemia 66 0.047
188
APN008 Apnea, Obstructive Sleep 64 0.047
189
P PRD008 Periodontitis 64 0.047
190
MSC007 Muscle Hypertrophy 64 0.047
191
MGK001 Megakaryocytic Leukemia 64 0.047
192
P GLM045 Glioma 63 0.047
193
P PSR002 Psoriasis 62 0.047
194
P HYP750 Hypertriglyceridemia, Familial 62 0.047
195
P VSC011 Vasculitis 62 0.047
196
P ORT004 Orthostatic Intolerance 62 0.047
197
P ENC018 Encephalopathy 61 0.047
198
HPT019 Hepatic Encephalopathy 60 0.047
199
CRD223 Cardiac Arrhythmia 60 0.047
200
SQM006 Squamous Cell Carcinoma 60 0.047
201
PRT013 Portal Hypertension 59 0.047
202
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.047
203
VSL002 Visual Epilepsy 59 0.047
204
P BRS044 Breast Adenocarcinoma 59 0.047
205
P BCL017 B-Cell Lymphoma 58 0.047
206
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.047
207
P PRP019 Peripheral Nervous System Disease 58 0.047
208
THR024 Thrombosis 57 0.047
209
VSC002 Vascular Dementia 57 0.047
210
P MYS005 Myositis 56 0.047
211
LST001 Listeriosis 56 0.047
212
P SZR006 Seizure Disorder 56 0.047
213
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.047
214
P ANT006 Antiphospholipid Syndrome 55 0.047
215
P HYP076 Hyperthyroidism 55 0.047
216
P SLM003 Salmonellosis 55 0.047
217
PLM010 Pulmonary Edema 54 0.047
218
PRP080 Peripheral Artery Disease 53 0.047
219
PST011 Pustulosis of Palm and Sole 52 0.047
220
PRV004 Periventricular Leukomalacia 52 0.047
221
P TMP001 Temporal Lobe Epilepsy 50 0.047
222
NTR046 Neutrophil Migration 50 0.047
223
RBF001 Riboflavin Deficiency 49 0.047
224
MYL013 Myeloperoxidase Deficiency 46 0.047
225
LKS001 Leukostasis 46 0.047
226
GLL048 Glial Tumor 45 0.047
227
URT010 Ureteral Obstruction 45 0.047
228
HPT004 Hepatic Coma 45 0.047
229
CRT015 Carotid Artery Occlusion 45 0.047
230
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.047
231
DBT008 Diabetic Angiopathy 44 0.047
232
GRN017 Granulocytopenia 44 0.047
234
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.047
235
DSR012 Disordered Steroidogenesis Due to Cytochrome P450 Oxidoreductase Deficiency 40 0.047
236
c CNG223 Congenital Methemoglobinemia 36 0.047
237
c GRN038 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type Iii 36 0.047
238
24D001 2,4-Dienoyl-Coa Reductase Deficiency 34 0.047
239
HYP572 Hypoganglionosis 28 0.047
240
c DLT002 Dilated Cardiomyopathy 79 0.039
241
P RTN008 Retinitis Pigmentosa 79 0.039
242
INS024 Insulin-Like Growth Factor I 79 0.039
243
MRF001 Marfan Syndrome 77 0.039
244
SVR004 Severe Combined Immunodeficiency 73 0.039
245
c THR092 Thrombophilia Due to Thrombin Defect 73 0.039
246
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.039
247
MSC157 Muscular Dystrophy, Duchenne Type 72 0.039
248
c LKM063 Leukemia, Chronic Myeloid 72 0.039
249
P EPL164 Epilepsy 71 0.039
250
P ATS364 Autism 70 0.039
251
DFC004 Deficiency Anemia 70 0.039
252
P AMY004 Amyloidosis 70 0.039
253
CRT072 Creutzfeldt-Jakob Disease 70 0.039
254
P ART022 Arthritis 69 0.039
255
P FRN006 Frontotemporal Dementia 68 0.039
256
P THR014 Thrombocytopenia 67 0.039
257
P HYP098 Hypereosinophilic Syndrome 67 0.039
258
c ATS007 Autism Spectrum Disorder 67 0.039
259
OST159 Osteogenic Sarcoma 66 0.039
260
P DMN002 Dementia 66 0.039
261
P ATR011 Atrial Fibrillation 66 0.039
262
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.039
263
P HRP006 Herpes Simplex 65 0.039
264
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.039
265
P NTR004 Neutropenia 63 0.039
266
P CRN300 Coronary Heart Disease 1 63 0.039
267
P ECT006 Ectodermal Dysplasia 62 0.039
268
P PRP029 Porphyria 62 0.039
269
ALC006 Alcoholic Hepatitis 61 0.039
270
c ACT071 Acute Kidney Failure 60 0.039
271
P MYC008 Myocarditis 59 0.039
272
P BND020 Bone Disease 59 0.039
273
CHL123 Chlamydia 59 0.039
274
ANT024 Anthrax Disease 58 0.039
275
PST028 Post-Traumatic Stress Disorder 58 0.039
276
EYD002 Eye Disease 58 0.039
277
P CND004 Candidiasis 58 0.039
278
P GLM007 Glomerulonephritis 57 0.039
279
MCR013 Microphthalmia 57 0.039
280
IRN002 Iron Metabolism Disease 57 0.039
281
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 57 0.039
282
P RHN004 Rhinitis 57 0.039
283
P FCL005 Focal Segmental Glomerulosclerosis 57 0.039
284
SCH014 Schistosomiasis 57 0.039
285
PHR003 Pharyngitis 57 0.039
286
SLC006 Silicosis 56 0.039
287
LMB062 Limb Ischemia 55 0.039
288
VSC003 Visceral Leishmaniasis 55 0.039
289
P GRV001 Graves' Disease 55 0.039
290
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 55 0.039
291
SYN007 Synovitis 54 0.039
292
HMS001 Hemosiderosis 54 0.039
293
PRS045 Prostatic Hypertrophy 53 0.039
294
P MNC007 Monocytic Leukemia 53 0.039
295
GTR002 Goiter 53 0.039
296
GST023 Gastric Ulcer 53 0.039
297
DMY004 Demyelinating Disease 52 0.039
298
PRP016 Paraplegia 52 0.039
299
c VRL010 Viral Hepatitis 52 0.039
300
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.039
301
THY030 Thyroid Gland Disease 52 0.039
302
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.039
303
PRS021 Prostatic Adenoma 51 0.039
304
P LCT001 Lactic Acidosis 51 0.039
305
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.039
306
PLR008 Pleurisy 50 0.039
307
P OVR082 Overgrowth Syndrome 50 0.039
308
P AGG001 Aggressive Periodontitis 50 0.039
309
MTB004 Metabolic Acidosis 50 0.039
310
PRS129 Prostatic Hyperplasia, Benign 49 0.039
311
WTH001 Withdrawal Disorder 48 0.039
312
c MTR002 Mitral Valve Insufficiency 48 0.039
313
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.039
314
CRN027 Corneal Neovascularization 47 0.039
315
ACT084 Acute Stress Disorder 47 0.039
316
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.039
317
RTN023 Retinitis 46 0.039
318
P VTR007 Vitreoretinopathy 46 0.039
319
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.039
320
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.039
321
P MTH007 Methemoglobinemia 46 0.039
322
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.039
323
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.039
324
SBC016 Subacute Delirium 44 0.039
325
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.039
326
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.039
327
CRB090 Cerebral Hypoxia 44 0.039
328
P DMY001 Demyelinating Polyneuropathy 43 0.039
329
NRR001 Neuroretinitis 42 0.039
330
EHR002 Ehrlichiosis 42 0.039
331
P RRH023 Rare Hereditary Hemochromatosis 41 0.039
332
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.039
333
SCR011 Scrapie 39 0.039
334
HRN029 Hearing Loss, Noise-Induced 37 0.039
335
PLC002 Plica Syndrome 36 0.039
337
KDN013 Kidney Hypertrophy 32 0.039
338
HMN002 Human Granulocytic Anaplasmosis 32 0.039
339
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.039
340
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.039
341
CRT065 Cortisone Reductase Deficiency 1 25 0.039
342
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.039
343
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.027
344
MYL069 Myeloma, Multiple 85 0.027
345
NRL016 Neural Tube Defects 82 0.027
346
P ATX030 Ataxia-Telangiectasia 82 0.027
347
c FNC027 Fanconi Anemia, Complementation Group a 81 0.027
348
P GLM040 Glioma Susceptibility 1 81 0.027
349
c NRF023 Neurofibromatosis, Type Ii 80 0.027
350
P LKM071 Leukemia, Chronic Lymphocytic 79 0.027
351
P LNG064 Lung Cancer Susceptibility 3 78 0.027
352
P MDL005 Medulloblastoma 77 0.027
353
CRV035 Cervical Cancer 76 0.027
354
PHN003 Phenylketonuria 75 0.027
355
P SCH015 Schizophrenia 74 0.027
356
CRH001 Crohn's Disease 74 0.027
357
c SPN225 Spondyloarthropathy 1 73 0.027
358
ANX010 Anxiety 73 0.027
359
P GRF003 Graft-Versus-Host Disease 72 0.027
360
GST040 Gastric Adenocarcinoma 70 0.027
361
MYL009 Myelodysplastic Syndrome 70 0.027
362
MYL005 Myelofibrosis 70 0.027
363
c GCH015 Gaucher Disease, Type I 70 0.027
364
P HYP061 Hypertrophic Cardiomyopathy 70 0.027
365
P FRG001 Fragile X Syndrome 70 0.027
366
SMT004 Smith-Lemli-Opitz Syndrome 70 0.027
367
LKC009 Leukocyte Adhesion Deficiency, Type I 69 0.027
368
P PNM007 Pneumonia 68 0.027
369
P MYC084 Mycobacterium Tuberculosis 1 68 0.027
370
P INF038 Influenza 68 0.027
371
BRN024 Bronchitis 68 0.027
372
RCK004 Rickets 68 0.027
373
P CRB048 Cerebral Cavernous Malformations 67 0.027
374
ALL003 Allergic Rhinitis 67 0.027
375
P PRP003 Porphyria Cutanea Tarda 67 0.027
376
P TRN020 Turner Syndrome 67 0.027
377
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.027
378
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.027
379
ALC007 Alcohol Dependence 66 0.027
380
GRG001 Greig Cephalopolysyndactyly Syndrome 66 0.027
381
P MNN013 Meningitis 66 0.027
382
P DRM053 Dermatitis, Atopic 66 0.027
383
P NRV007 Nervous System Disease 66 0.027
384
c SML038 Small Cell Cancer of the Lung 65 0.027
385
TTN003 Tetanus 65 0.027
386
KWS002 Kawasaki Disease 65 0.027
387
c DBT099 Diabetes Mellitus, Type I 65 0.027
388
CLN015 Colon Adenocarcinoma 65 0.027
389
CRB011 Cerebrotendinous Xanthomatosis 65 0.027
390
P DBT009 Diabetes Mellitus 64 0.027
391
ANG020 Angiosarcoma 64 0.027
392
NRM005 Neuromuscular Disease 64 0.027
393
c JVN010 Juvenile Rheumatoid Arthritis 64 0.027
394
P GLC113 Galactosemia I 64 0.027
395
RFS006 Refsum Disease, Classic 64 0.027
396
OST017 Osteomyelitis 64 0.027
397
c DPH024 Diaphragmatic Hernia, Congenital 63 0.027
398
P GCH001 Gaucher's Disease 63 0.027
399
P HML002 Hemolytic Anemia 63 0.027
400
P END044 Endometriosis 63 0.027
401
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.027
402
c HPT001 Hepatitis C 62 0.027
403
c BRN108 Branchiootic Syndrome 1 62 0.027
404
c SVR001 Severe Acute Respiratory Syndrome 62 0.027
405
P ESP024 Esophagitis 62 0.027
406
P ART023 Arthropathy 62 0.027
407
CTN007 Cutaneous Leishmaniasis 62 0.027
408
MDD011 Mood Disorder 62 0.027
409
PSR001 Psoriatic Arthritis 61 0.027
411
OST003 Osteonecrosis 61 0.027
412
INT002 Intermittent Claudication 61 0.027
413
P ENC004 Encephalitis 61 0.027
414
P HMN010 Hemangioma 61 0.027
415
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.027
416
P KDN017 Kidney Cancer 60 0.027
417
P NPH012 Nephrotic Syndrome 60 0.027
418
WLL001 Williams-Beuren Syndrome 60 0.027
419
P TXP001 Toxoplasmosis 60 0.027
420
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.027
421
P VNT002 Ventricular Septal Defect 60 0.027
422
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.027
423
ACQ007 Acquired Immunodeficiency Syndrome 60 0.027
424
DNG002 Dengue Hemorrhagic Fever 60 0.027
425
RHM001 Rheumatic Fever 60 0.027
426
ORL011 Oral Cancer 60 0.027
427
INS001 Insulinoma 60 0.027
428
HYD002 Hydronephrosis 60 0.027
429
P GLY013 Glycogen Storage Disease 60 0.027
430
P CHR285 Chronic Myelomonocytic Leukemia 60 0.027
431
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.027
432
PNM001 Pneumocystosis 59 0.027
433
P SLP005 Sleep Disorder 59 0.027
434
PLM033 Pulmonary Embolism 59 0.027
435
PRN019 Perinatal Necrotizing Enterocolitis 59 0.027
436
BRN002 Bronchiolitis 59 0.027
437
IRN001 Iron Deficiency Anemia 59 0.027
438
P DNG005 Dengue Virus 59 0.027
439
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.027
440
PPT005 Peptic Ulcer Disease 59 0.027
441
P ANP001 Anaplastic Large Cell Lymphoma 58 0.027
442
GLB001 Gilbert Syndrome 58 0.027
443
CRD132 Cardiac Conduction Defect 58 0.027
444
FML063 Familial Glucocorticoid Deficiency 58 0.027
445
CCC001 Coccidioidomycosis 58 0.027
446
P MTR012 Mitral Valve Disease 58 0.027
447
CRV038 Cervical Squamous Cell Carcinoma 58 0.027
448
EXT034 Extrinsic Allergic Alveolitis 58 0.027
449
P INF032 Infertility 57 0.027
450
P UVT001 Uveitis 57 0.027
451
c MST023 Mesothelioma, Malignant 57 0.027
452
TNS005 Tonsillitis 57 0.027
453
P FTL001 Fetal Alcohol Syndrome 57 0.027
454
LYS003 Lysinuric Protein Intolerance 57 0.027
455
P PYL005 Pyelonephritis 56 0.027
456
P PLY011 Polycystic Ovary Syndrome 56 0.027
457
c ACT134 Acute Liver Failure 56 0.027
458
ADN027 Adenomyosis 56 0.027
459
ERY051 Erythroleukemia, Familial 56 0.027
460
P MTC069 Mitochondrial Disorders 56 0.027
461
P PNL012 Penile Cancer 56 0.027
462
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 56 0.027
463
EMB004 Embryonal Carcinoma 56 0.027
464
MCS002 Mucositis 56 0.027
465
P PLY180 Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy 1 56 0.027
466
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.027
467
MCL006 Macular Retinal Edema 55 0.027
468
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.027
469
CHR100 Chronic Ulcer of Skin 55 0.027
470
PRP030 Purpura 54 0.027
471
TRD006 Tardive Dyskinesia 54 0.027
472
CRY003 Cryptosporidiosis 54 0.027
473
RST011 Restrictive Dermopathy, Lethal 54 0.027
474
HLL004 Hellp Syndrome 54 0.027
475
PPL022 Papilloma 54 0.027
476
SLP001 Sleeping Sickness 54 0.027
477
P TRM003 Tremor 54 0.027
478
P EPD016 Epidermolysis Bullosa 53 0.027
479
RHM028 Rheumatic Heart Disease 53 0.027
480
HRT012 Heart Valve Disease 53 0.027
481
P HMC002 Homocystinuria 53 0.027
482
CRH005 Crohn's Colitis 53 0.027
483
P RNL017 Renal Oncocytoma 53 0.027
484
ACR014 Acral Lentiginous Melanoma 53 0.027
485
MST005 Mastitis 53 0.027
486
NNT012 Neonatal Jaundice 53 0.027
487
OVR059 Ovary Adenocarcinoma 53 0.027
488
c CNT035 Central Nervous System Disease 52 0.027
489
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.027
490
PLM014 Pleomorphic Adenoma 52 0.027
491
TRC096 Trichothiodystrophy 52 0.027
492
c SPN291 Spinocerebellar Ataxia 7 52 0.027
493
P DDN001 Duodenal Ulcer 52 0.027
494
P THY032 Thyroiditis 52 0.027
495
PPT001 Peptic Esophagitis 52 0.027
496
ART074 Aortic Dissection 52 0.027
497
TLN003 Telangiectasis 52 0.027
498
P TRT010 Teratoma 52 0.027
499
PNG002 Pain Agnosia 51 0.027
500
OCL069 Ocular Motor Apraxia 51 0.027
501
KRT009 Keratosis 51 0.027
502
ENT011 Enterocolitis 51 0.027
503
ACH005 Achalasia 51 0.027
504
IRK001 Irak4 Deficiency 51 0.027
505
GNG012 Gingival Overgrowth 51 0.027
506
TLR001 Tularemia 51 0.027
507
CRV040 Cervix Carcinoma 51 0.027
508
CRN030 Coronary Stenosis 50 0.027
509
P ESN008 Eosinophilic Pneumonia 50 0.027
510
CRT013 Carotid Stenosis 50 0.027
511
FSC004 Fasciitis 50 0.027
512
NPH018 Nephrogenic Systemic Fibrosis 50 0.027
513
HRT011 Heart Septal Defect 50 0.027
514
P ATR005 Atrophic Gastritis 50 0.027
515
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 49 0.027
516
P MYT002 Myotonic Dystrophy 49 0.027
517
HYP006 Hypertensive Heart Disease 49 0.027
518
GYN001 Gynecomastia 49 0.027
519
PLP001 Pulpitis 49 0.027
520
CCN002 Cocaine Abuse 49 0.027
521
XNT003 Xanthomatosis 49 0.027
522
MTC005 Mitochondrial Metabolism Disease 49 0.027
523
EPD006 Epidermolysis Bullosa Acquisita 49 0.027
524
URM002 Uremia 49 0.027
525
SPH001 Sapho Syndrome 48 0.027
526
NCR007 Necrotizing Fasciitis 48 0.027
527
P RNV001 Renovascular Hypertension 48 0.027
528
PLM035 Pulmonary Eosinophilia 48 0.027
529
SPL018 Splenomegaly 48 0.027
530
HYP068 Hyperostosis 48 0.027
531
DGN001 Degenerative Disc Disease 48 0.027
532
CHL147 Chlamydia Pneumonia 48 0.027
533
BNN003 Bone Inflammation Disease 48 0.027
534
FBR032 Fibromuscular Dysplasia 48 0.027
535
PRP007 Priapism 47 0.027
536
c MLG069 Malignant Hypertension 47 0.027
537
P RNL015 Renal Hypertension 47 0.027
538
KHN001 Kuhnt-Junius Degeneration 47 0.027
539
P CRC039 Coarctation of Aorta 47 0.027
540
STR103 Streptococcus Pneumonia 47 0.027
541
ANT003 Antley-Bixler Syndrome 47 0.027
542
CHR074 Choriocarcinoma 47 0.027
543
c OPT051 Opitz Gbbb Syndrome, Type I 47 0.027
544
ATN005 Autonomic Dysfunction 46 0.027
545
c ACT076 Acute Myocarditis 46 0.027
546
PSD009 Pseudohermaphroditism 46 0.027
547
PDT035 Pediatric Systemic Lupus Erythematosus 46 0.027
548
P BNG032 Benign Mesothelioma 46 0.027
549
HDN002 Head Injury 46 0.027
550
PRX001 Peroxisomal Disease 46 0.027
551
SGN002 Signet Ring Cell Adenocarcinoma 45 0.027
552
c TRC022 Tricuspid Valve Insufficiency 45 0.027
553
CYN002 Cyanosis, Transient Neonatal 45 0.027
554
CHR466 Chronic Thromboembolic Pulmonary Hypertension 45 0.027
555
URL001 Urolithiasis 45 0.027
556
ACT003 Acute Kidney Tubular Necrosis 45 0.027
557
c ATM099 Autoimmune Uveitis 45 0.027
558
SPS057 Spasticity 45 0.027
559
ASP026 Asplenia, Isolated Congenital 44 0.027
560
P CHR345 Chronic Pain 44 0.027
561
P MTC004 Mitochondrial Encephalomyopathy 44 0.027
562
TNG009 Tongue Squamous Cell Carcinoma 44 0.027
563
SPN119 Spondylarthropathy 44 0.027
564
CVD001 Covid-19 44 0.027
565
c FTL006 Fetal Alcohol Spectrum Disorder 43 0.027
566
ORL015 Oral Squamous Cell Carcinoma 43 0.027
567
ILC002 Ileocolitis 43 0.027
568
HMP009 Haemophilus Influenzae 43 0.027
569
DRG002 Drug-Induced Hepatitis 43 0.027
570
HYP457 Hypertrophic Scars 42 0.027
571
MST004 Mast Cell Neoplasm 42 0.027
572
P AVS003 Avascular Necrosis 42 0.027
573
PNM013 Pneumococcal Meningitis 42 0.027
574
EPT021 Epithelial Recurrent Erosion Dystrophy 42 0.027
575
ATX019 Ataxia with Vitamin E Deficiency 42 0.027
576
c MLG079 Malignant Pleural Mesothelioma 42 0.027
577
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.027
578
c ATS307 Autosomal Recessive Cerebellar Ataxia 42 0.027
579
OCL052 Ocular Dominance 42 0.027
580
P ALK015 Alk-Positive Anaplastic Large Cell Lymphoma 40 0.027
581
ALC005 Alcoholic Pancreatitis 40 0.027
582
KLD004 Keloid Disorder 40 0.027
583
PLY100 Polyploidy 40 0.027
584
P MGL010 Megalencephalic Leukoencephalopathy with Subcortical Cysts 2a 40 0.027
585
P TRC031 Trichorhinophalangeal Syndrome 40 0.027
586
CRB086 Cerebral Aneurysms 40 0.027
587
c PRG020 Paragangliomas 3 39 0.027
589
BLR002 Bile Reflux 39 0.027
590
AMN006 Aminoaciduria 38 0.027
591
EXT007 Extracutaneous Mastocytoma 38 0.027
592
OVR094 Ovarian Epithelial Cancer 38 0.027
593
VSM001 Vasomotor Rhinitis 38 0.027
594
CDQ001 Cauda Equina Syndrome 38 0.027
595
ACY011 Acyl-Coa Dehydrogenase Deficiency 38 0.027
596
OST006 Osteoblastoma 38 0.027
597
CRT004 Carotid Artery Thrombosis 38 0.027
598
STR077 Streptococcal Toxic-Shock Syndrome 37 0.027
599
PNB004 Panbronchiolitis, Diffuse 37 0.027
600
P CRB059 Cerebellar Degeneration 37 0.027
601
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 37 0.027
602
SYS071 Systemic Autoimmune Disease 37 0.027
603
HYP026 Hypoglycemic Coma 36 0.027
604
MYC017 Mycobacterium Kansasii 36 0.027
606
MTH026 Methemoglobinemia Due to Deficiency of Methemoglobin Reductase 36 0.027
607
ECT108 Ectodermal Dysplasia and Immunodeficiency 1 36 0.027
608
c NTR047 Neutropenia, Severe Congenital, 1, Autosomal Dominant 36 0.027
609
HYP114 Hypertensive Nephropathy 36 0.027
610
LCH001 Leech Infestation 35 0.027
611
c ATM022 Autoimmune Myocarditis 35 0.027
612
PRM329 Premature Aging 35 0.027
613
NRX001 Neuroaxonal Dystrophy 35 0.027
614
c NNS007 Nonsyndromic Deafness 35 0.027
615
DXR001 Doxorubicin Induced Cardiomyopathy 33 0.027
616
GNT167 Genetic Obesity 33 0.027
617
ANT042 Antley-Bixler Syndrome with Genital Anomalies and Disordered Steroidogenesis 32 0.027
618
c RTN140 Retinitis Pigmentosa 67 32 0.027
619
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.027
621
INF021 Infant Gynecomastia 31 0.027
622
c RTN143 Retinitis Pigmentosa 47 30 0.027
623
CVR010 Cavernous Malformation 30 0.027
624
MLG163 Malignant Tumor of Penis 29 0.027
625
MGL012 Megaloblastic Anemia Due to Dihydrofolate Reductase Deficiency 28 0.027
626
CTN027 Cutaneous Mastocytoma 28 0.027
627
ARG004 Argyria 27 0.027
628
CYT018 Cytochrome P450 2d6 Variant 27 0.027
629
MST020 Mast Cell Activation Syndrome 26 0.027
630
GLY111 Glycogen Storage Disease Due to Glucose-6-Phosphatase Deficiency Type Ib 26 0.027
631
STN013 Stenotrophomonas Maltophilia Infection 25 0.027
632
URT049 Urate Oxidase, Pseudogene 25 0.027
633
CRT066 Cortisone Reductase Deficiency 2 24 0.027
634
TXC004 Toxic Diffuse Goiter 24 0.027
635
P STR035 Streptococcal Group a Invasive Disease 23 0.027
636
c TRN047 Transient Congenital Hypothyroidism 23 0.027
637
c RNG019 Ring Chromosome 3 22 0.027
638
CRB087 Cerebral Arteriosclerosis 22 0.027
639
BRN147 Brain Inflammatory Disease 9 0.027
Content
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