Search results for nadph

618 hits were found for nadph

# Family MCID Name MIFTS Score
1
MTH072 Methemoglobin Reductase Deficiency 19 2.930
2
P CHR012 Chronic Granulomatous Disease 69 0.398
3
P VSC007 Vascular Disease 65 0.237
4
HYP066 Hyperglycemia 63 0.205
5
c MCR113 Microvascular Complications of Diabetes 3 55 0.195
6
c MCR120 Microvascular Complications of Diabetes 7 48 0.195
7
c MCR130 Microvascular Complications of Diabetes 6 42 0.195
8
c MCR133 Microvascular Complications of Diabetes 4 42 0.195
9
ATH013 Atherosclerosis Susceptibility 68 0.178
10
ISC004 Ischemia 62 0.178
11
HYP266 Hypoxia 58 0.176
12
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.167
13
c ACT210 Acute Respiratory Distress Syndrome 59 0.157
14
P PLM037 Pulmonary Hypertension 69 0.149
15
P MCR115 Microvascular Complications of Diabetes 5 67 0.144
16
CRB004 Cerebral Artery Occlusion 38 0.144
17
PRT037 Pertussis 66 0.135
18
TRM010 Traumatic Brain Injury 54 0.129
19
BRN071 Brain Injury 51 0.129
20
P CLR023 Colorectal Cancer 100 0.126
21
P SLP006 Sleep Apnea 71 0.123
22
P NRB010 Neuroblastoma 1 66 0.119
23
P ALZ034 Alzheimer Disease 90 0.113
24
P LVR013 Liver Disease 71 0.113
25
P PLM036 Pulmonary Fibrosis 66 0.113
26
IDP011 Idiopathic Interstitial Pneumonia 65 0.113
27
CRB039 Cerebrovascular Disease 71 0.109
28
c PRC016 Pre-Eclampsia 63 0.109
29
ATM095 Autoimmune Disease 62 0.109
30
IMP005 Impotence 53 0.109
31
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.105
32
P HNT016 Huntington Disease 72 0.105
33
BCT022 Bacterial Infectious Disease 57 0.105
34
P LTR001 Lateral Sclerosis 56 0.105
35
CYT002 Cytokine Deficiency 46 0.105
36
P HYP086 Hypothyroidism 70 0.101
37
LNG099 Lung Disease 62 0.101
38
47X002 47,xyy 49 0.101
39
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.101
40
GLB002 Glioblastoma 74 0.097
41
SPN186 Spinal Cord Injury 63 0.097
42
GLB015 Glioblastoma Multiforme 60 0.097
43
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.097
44
P HRT032 Heart Disease 78 0.093
45
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.093
46
c HYP836 Hypercholesterolemia, Familial, 1 74 0.093
47
P KDN018 Kidney Disease 73 0.093
48
CNG034 Congestive Heart Failure 69 0.093
49
BRR014 Barrett Esophagus 67 0.093
50
P ADN016 Adenocarcinoma 65 0.093
51
HMC014 Homocysteinemia 54 0.093
52
HLX001 Helix Syndrome 46 0.093
53
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.089
54
OST012 Osteoarthritis 80 0.089
55
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.089
56
c CHR684 Chronic Kidney Disease 68 0.089
57
FTT001 Fatty Liver Disease 63 0.089
58
ART140 Arteries, Anomalies of 60 0.089
59
P INF037 Inflammatory Bowel Disease 57 0.089
60
GRN051 Granulomatous Disease, Chronic, X-Linked 55 0.089
61
RNL077 Renal Fibrosis 49 0.089
62
ANX004 Anoxia 44 0.089
63
ALL014 Allergic Encephalomyelitis 40 0.089
64
c LKM061 Leukemia, Acute Myeloid 84 0.084
65
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.084
66
P CRN018 Coronary Artery Anomaly 67 0.084
67
ALL026 Allergic Hypersensitivity Disease 65 0.084
68
c SCL052 Scleroderma, Familial Progressive 62 0.084
69
BRN004 Brain Edema 57 0.084
70
NNL006 Non-Alcoholic Steatohepatitis 53 0.084
71
P HPT023 Hepatocellular Carcinoma 99 0.080
72
P PNC035 Pancreatic Cancer 86 0.080
73
CYS001 Cystic Fibrosis 84 0.080
74
c ATR087 Atrial Standstill 1 76 0.080
75
P MYL006 Myeloid Leukemia 61 0.080
76
END030 End Stage Renal Failure 60 0.080
77
AGN016 Aging 58 0.080
78
CHL014 Cholera 58 0.080
79
P SCK005 Sickle Cell Disease 53 0.080
80
RTN020 Retinal Vascular Disease 49 0.080
81
P GRN048 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Negative 41 0.080
82
PPL052 Papillomatosis, Confluent and Reticulated 34 0.080
83
PST092 Posttransplant Acute Limbic Encephalitis 29 0.080
84
P BRS047 Breast Cancer 99 0.074
85
c HYP595 Hypertension, Essential 87 0.074
86
STR067 Stroke, Ischemic 82 0.074
87
P MSC005 Muscular Dystrophy 68 0.074
88
P ASP006 Aspergillosis 67 0.074
89
THY029 Thyroid Carcinoma 62 0.074
90
P CTR002 Cataract 62 0.074
91
HLC007 Helicobacter Pylori Infection 61 0.074
92
c ACT027 Acute Pancreatitis 60 0.074
93
ADN018 Adenoma 60 0.074
94
48X005 48,xyyy 37 0.074
95
c GRN049 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I 37 0.074
96
PLY150 Polykaryocytosis Inducer 31 0.074
97
P PRS040 Prostate Cancer 97 0.069
99
P GST053 Gastric Cancer 85 0.069
100
c CNG006 Congenital Hypothyroidism 65 0.069
101
SKN016 Skin Disease 64 0.069
102
LPD008 Lipid Metabolism Disorder 64 0.069
103
CLT003 Colitis 63 0.069
104
STT001 Status Epilepticus 61 0.069
105
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.069
106
HYP014 Hyperuricemia 52 0.069
107
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.069
108
IMM167 Immune Deficiency Disease 79 0.063
109
P OST002 Osteoporosis 79 0.063
110
P PRK057 Parkinson Disease, Late-Onset 77 0.063
111
c HPT073 Hepatitis C Virus 74 0.063
112
P PHC003 Pheochromocytoma 71 0.063
113
ART016 Aortic Aneurysm 71 0.063
114
c EXD008 Exudative Vitreoretinopathy 1 69 0.063
115
c MCR129 Microvascular Complications of Diabetes 1 67 0.063
116
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.063
117
P HRS035 Hirschsprung Disease 1 65 0.063
118
CHL068 Cholestasis 61 0.063
119
P ALC033 Alcohol Use Disorder 58 0.063
120
P GST044 Gastritis 58 0.063
121
P PRN023 Prion Disease 57 0.063
122
P FBR017 Fibrosarcoma 57 0.063
123
P ART021 Arteriosclerosis 56 0.063
124
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.063
125
BNR002 Bone Resorption Disease 51 0.063
126
ADR040 Adrenal Gland Pheochromocytoma 51 0.063
127
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.063
128
c MCR112 Microvascular Complications of Diabetes 2 42 0.063
129
P LNG032 Lung Cancer 99 0.056
130
c SYS001 Systemic Lupus Erythematosus 88 0.056
131
P RHM011 Rheumatoid Arthritis 82 0.056
132
P BLD134 Bladder Cancer 79 0.056
133
ULC004 Ulcerative Colitis 75 0.056
134
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.056
135
P MYC007 Myocardial Infarction 74 0.056
136
P RTN024 Retinoblastoma 74 0.056
137
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.056
138
HMN044 Human Immunodeficiency Virus Type 1 73 0.056
139
P MLT020 Multiple Sclerosis 73 0.056
140
LYM133 Lymphoma, Hodgkin, Classic 70 0.056
141
P LKM002 Leukemia 69 0.056
142
GST092 Gastroesophageal Reflux 68 0.056
143
MLN008 Melanoma 68 0.056
144
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.056
145
CHG001 Chagas Disease 66 0.056
146
ACT119 Acute Promyelocytic Leukemia 63 0.056
147
TXC005 Toxic Shock Syndrome 63 0.056
148
P LPS004 Lupus Erythematosus 62 0.056
149
TRN015 Transient Cerebral Ischemia 62 0.056
150
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.056
151
ANR040 Aneurysm 60 0.056
152
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.056
153
P RTN016 Retinal Degeneration 56 0.056
154
DBT010 Diabetic Neuropathy 56 0.056
155
GLC003 Glucose Intolerance 55 0.056
156
P PLY019 Polyneuropathy 55 0.056
157
P ECL001 Eclampsia 53 0.056
158
P RTN018 Retinal Disease 53 0.056
159
RTN003 Retinal Ischemia 52 0.056
160
P MSC003 Muscular Atrophy 52 0.056
161
ATS010 Autosomal Recessive Disease 49 0.056
162
c INV001 Invasive Aspergillosis 48 0.056
163
c GRN050 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type Ii 47 0.056
164
c FML008 Familial Retinoblastoma 46 0.056
165
c PCH010 Pachyonychia Congenita 3 43 0.056
166
CYT014 Cytochrome P450 Oxidoreductase Deficiency 33 0.056
167
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.049
168
END057 Endometrial Cancer 74 0.049
169
PRP027 Peripheral Vascular Disease 72 0.049
170
LPD012 Lipoid Congenital Adrenal Hyperplasia 71 0.049
171
PNC129 Pancreatic Adenocarcinoma 69 0.049
172
P SYS005 Systemic Scleroderma 68 0.049
173
HYP056 Hypoglycemia 68 0.049
174
P NSP012 Nasopharyngeal Carcinoma 67 0.049
175
P ATR011 Atrial Fibrillation 67 0.049
176
LVR012 Liver Cirrhosis 67 0.049
177
P SKN015 Skin Carcinoma 67 0.049
178
PRT036 Peritonitis 66 0.049
179
MLD001 Melioidosis 66 0.049
180
P PRD008 Periodontitis 66 0.049
181
ANG054 Angina Pectoris 66 0.049
182
MGK001 Megakaryocytic Leukemia 65 0.049
183
P VSC011 Vasculitis 64 0.049
184
P ENC018 Encephalopathy 64 0.049
185
LSH001 Leishmaniasis 64 0.049
186
APN008 Apnea, Obstructive Sleep 64 0.049
187
P GLM045 Glioma 64 0.049
188
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.049
189
P MYP004 Myopathy 63 0.049
190
P HYP750 Hypertriglyceridemia, Familial 62 0.049
191
c ART138 Aortic Aneurysm, Familial Abdominal, 1 62 0.049
192
CRD223 Cardiac Arrhythmia 61 0.049
193
PRT013 Portal Hypertension 61 0.049
194
P BCL017 B-Cell Lymphoma 61 0.049
195
P PNC044 Pancreatitis 61 0.049
196
HPT019 Hepatic Encephalopathy 60 0.049
197
P SZR006 Seizure Disorder 59 0.049
198
P BRS044 Breast Adenocarcinoma 59 0.049
199
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.049
200
VSL002 Visual Epilepsy 58 0.049
201
THR024 Thrombosis 58 0.049
202
HPT022 Hepatoblastoma 58 0.049
203
P NRP001 Neuropathy 57 0.049
204
VSC002 Vascular Dementia 57 0.049
205
RLP002 Relapsing-Remitting Multiple Sclerosis 57 0.049
206
P ANT006 Antiphospholipid Syndrome 56 0.049
207
PLM010 Pulmonary Edema 56 0.049
208
HYP060 Hyperinsulinism 55 0.049
209
P HYP076 Hyperthyroidism 55 0.049
210
LST001 Listeriosis 55 0.049
211
P MYS005 Myositis 54 0.049
212
P SLM003 Salmonellosis 54 0.049
213
PRP080 Peripheral Artery Disease 51 0.049
214
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.049
215
PRV004 Periventricular Leukomalacia 50 0.049
216
NTR046 Neutrophil Migration 49 0.049
217
GLL048 Glial Tumor 48 0.049
218
MYL013 Myeloperoxidase Deficiency 47 0.049
219
GRN017 Granulocytopenia 46 0.049
220
RBF001 Riboflavin Deficiency 46 0.049
221
CRT015 Carotid Artery Occlusion 44 0.049
222
LKS001 Leukostasis 43 0.049
223
P KLZ004 Kala-Azar 1 43 0.049
224
DBT008 Diabetic Angiopathy 42 0.049
225
HPT004 Hepatic Coma 42 0.049
227
c GRN038 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type Iii 36 0.049
228
DSR012 Disordered Steroidogenesis Due to Cytochrome P450 Oxidoreductase Deficiency 36 0.049
229
c HRD146 Hereditary Methemoglobinemia 29 0.049
230
HYP572 Hypoganglionosis 28 0.049
231
c DLT002 Dilated Cardiomyopathy 81 0.040
232
INS024 Insulin-Like Growth Factor I 79 0.040
233
P RTN008 Retinitis Pigmentosa 77 0.040
234
DFC004 Deficiency Anemia 77 0.040
235
P SCH015 Schizophrenia 76 0.040
236
MRF001 Marfan Syndrome 75 0.040
237
c THR092 Thrombophilia Due to Thrombin Defect 74 0.040
238
SVR004 Severe Combined Immunodeficiency 74 0.040
239
c LKM063 Leukemia, Chronic Myeloid 74 0.040
240
P EPL164 Epilepsy 73 0.040
241
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.040
242
P AMY004 Amyloidosis 71 0.040
243
MSC157 Muscular Dystrophy, Duchenne Type 70 0.040
244
P INF038 Influenza 69 0.040
245
P DMN002 Dementia 68 0.040
246
P ORT004 Orthostatic Intolerance 68 0.040
247
BRK010 Burkitt Lymphoma 68 0.040
248
CRT072 Creutzfeldt-Jakob Disease 67 0.040
249
P HYP098 Hypereosinophilic Syndrome 67 0.040
250
P THR014 Thrombocytopenia 67 0.040
251
P HRP006 Herpes Simplex 66 0.040
252
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.040
253
MSC007 Muscle Hypertrophy 65 0.040
254
P PRP019 Peripheral Nervous System Disease 64 0.040
255
P NTR004 Neutropenia 64 0.040
256
P PSR002 Psoriasis 63 0.040
257
P FCL005 Focal Segmental Glomerulosclerosis 63 0.040
258
MCR013 Microphthalmia 62 0.040
259
P CND004 Candidiasis 61 0.040
260
SQM006 Squamous Cell Carcinoma 60 0.040
261
CHL123 Chlamydia 60 0.040
262
c ACT071 Acute Kidney Failure 60 0.040
263
P MYC008 Myocarditis 60 0.040
264
ALC006 Alcoholic Hepatitis 60 0.040
265
BND020 Bone Disease 60 0.040
266
PST028 Post-Traumatic Stress Disorder 60 0.040
267
P INF032 Infertility 60 0.040
268
P RHN004 Rhinitis 59 0.040
269
EYD002 Eye Disease 59 0.040
270
P GLM007 Glomerulonephritis 58 0.040
271
P PRP029 Porphyria 58 0.040
272
ECT006 Ectodermal Dysplasia 58 0.040
273
IRN002 Iron Metabolism Disease 58 0.040
274
SCH014 Schistosomiasis 57 0.040
275
P GRV001 Graves' Disease 57 0.040
276
ANT024 Anthrax Disease 56 0.040
277
ALL006 Allergic Asthma 56 0.040
278
P LYM031 Lymphocytic Leukemia 56 0.040
279
c VRL010 Viral Hepatitis 56 0.040
280
PHR003 Pharyngitis 56 0.040
281
SYN007 Synovitis 55 0.040
282
SLC006 Silicosis 55 0.040
283
VSC003 Visceral Leishmaniasis 55 0.040
284
PRS045 Prostatic Hypertrophy 55 0.040
285
PRP016 Paraplegia 54 0.040
286
GTR002 Goiter 54 0.040
287
HMS001 Hemosiderosis 54 0.040
288
DMY004 Demyelinating Disease 54 0.040
289
P TMP001 Temporal Lobe Epilepsy 53 0.040
290
THY030 Thyroid Gland Disease 53 0.040
291
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 53 0.040
292
GST023 Gastric Ulcer 53 0.040
293
PNG002 Pain Agnosia 52 0.040
294
P MNC007 Monocytic Leukemia 52 0.040
295
P LCT001 Lactic Acidosis 52 0.040
296
PRS021 Prostatic Adenoma 52 0.040
297
DYS014 Dyspepsia 51 0.040
298
OVR082 Overgrowth Syndrome 51 0.040
299
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.040
300
PST011 Pustulosis of Palm and Sole 51 0.040
301
LMB062 Limb Ischemia 50 0.040
302
P AGG001 Aggressive Periodontitis 50 0.040
303
PLR008 Pleurisy 50 0.040
304
PRS129 Prostatic Hyperplasia, Benign 49 0.040
305
MTB004 Metabolic Acidosis 48 0.040
306
CRN027 Corneal Neovascularization 48 0.040
307
VTR007 Vitreoretinopathy 48 0.040
308
WTH001 Withdrawal Disorder 47 0.040
309
c CHR283 Chronic Inflammatory Demyelinating Polyneuropathy 47 0.040
310
P MTH007 Methemoglobinemia 47 0.040
311
URT010 Ureteral Obstruction 46 0.040
312
RTN023 Retinitis 46 0.040
313
NRR001 Neuroretinitis 46 0.040
314
CRB090 Cerebral Hypoxia 45 0.040
315
EHR002 Ehrlichiosis 44 0.040
316
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.040
317
SBC016 Subacute Delirium 43 0.040
318
P DMY001 Demyelinating Polyneuropathy 43 0.040
319
ACT084 Acute Stress Disorder 42 0.040
320
P RRH023 Rare Hereditary Hemochromatosis 41 0.040
321
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 40 0.040
322
HRN029 Hearing Loss, Noise-Induced 38 0.040
323
SCR011 Scrapie 37 0.040
324
HMN002 Human Granulocytic Anaplasmosis 35 0.040
326
c DNT047 Dentinogenesis Imperfecta Type 2 34 0.040
327
24D001 2,4-Dienoyl-Coa Reductase Deficiency 32 0.040
328
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 29 0.040
329
KDN013 Kidney Hypertrophy 27 0.040
330
CRT084 Creatinine Clearance Quantitative Trait Locus 26 0.040
331
CRT065 Cortisone Reductase Deficiency 1 25 0.040
332
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.028
333
MYL069 Myeloma, Multiple 85 0.028
334
P ATX030 Ataxia-Telangiectasia 83 0.028
335
c LKM071 Leukemia, Chronic Lymphocytic 81 0.028
336
c FNC027 Fanconi Anemia, Complementation Group a 81 0.028
337
AST005 Asthma 80 0.028
338
P LNG064 Lung Cancer Susceptibility 3 79 0.028
339
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.028
340
P MDL005 Medulloblastoma 78 0.028
341
P NRF023 Neurofibromatosis, Type Ii 77 0.028
342
CRH001 Crohn's Disease 75 0.028
343
ANX010 Anxiety 75 0.028
344
c SPN225 Spondyloarthropathy 1 74 0.028
345
PHN003 Phenylketonuria 73 0.028
346
MYL009 Myelodysplastic Syndrome 72 0.028
347
P GRF003 Graft-Versus-Host Disease 71 0.028
348
P ART022 Arthritis 71 0.028
349
P PNM007 Pneumonia 71 0.028
350
BRN024 Bronchitis 70 0.028
351
RCK004 Rickets 70 0.028
352
FRN006 Frontotemporal Dementia 70 0.028
353
P LYM118 Lymphoma 70 0.028
354
c ATS007 Autism Spectrum Disorder 69 0.028
355
P MYC084 Mycobacterium Tuberculosis 1 69 0.028
356
MYL005 Myelofibrosis 69 0.028
357
ALL003 Allergic Rhinitis 69 0.028
358
P FRG001 Fragile X Syndrome 69 0.028
359
P ATS364 Autism 68 0.028
360
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.028
361
P HYP061 Hypertrophic Cardiomyopathy 68 0.028
362
ALC007 Alcohol Dependence 68 0.028
363
P NRV007 Nervous System Disease 68 0.028
364
P DRM053 Dermatitis, Atopic 68 0.028
365
c JVN010 Juvenile Rheumatoid Arthritis 67 0.028
366
SMT004 Smith-Lemli-Opitz Syndrome 67 0.028
367
P MNN013 Meningitis 67 0.028
368
c SML038 Small Cell Cancer of the Lung 67 0.028
369
OST159 Osteogenic Sarcoma 67 0.028
370
GST040 Gastric Adenocarcinoma 67 0.028
371
c DPH024 Diaphragmatic Hernia, Congenital 66 0.028
372
P PRP003 Porphyria Cutanea Tarda 66 0.028
373
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.028
374
P CRB048 Cerebral Cavernous Malformations 65 0.028
375
c GCH015 Gaucher Disease, Type I 65 0.028
376
P NPH012 Nephrotic Syndrome 65 0.028
377
KWS002 Kawasaki Disease 65 0.028
378
CLN015 Colon Adenocarcinoma 65 0.028
379
P HML002 Hemolytic Anemia 64 0.028
380
LKC009 Leukocyte Adhesion Deficiency, Type I 64 0.028
381
P TRC102 Trichothiodystrophy 1, Photosensitive 64 0.028
382
P ENC004 Encephalitis 64 0.028
383
P GCH001 Gaucher's Disease 63 0.028
384
PSR001 Psoriatic Arthritis 63 0.028
385
P END044 Endometriosis 63 0.028
386
GLC006 Galactosemia 63 0.028
387
MDD011 Mood Disorder 62 0.028
388
c BRN108 Branchiootic Syndrome 1 62 0.028
389
P HMN010 Hemangioma 62 0.028
390
OST003 Osteonecrosis 62 0.028
391
RFS006 Refsum Disease, Classic 62 0.028
392
NRM005 Neuromuscular Disease 62 0.028
393
P ESP024 Esophagitis 62 0.028
394
TTN003 Tetanus 62 0.028
395
c HPT001 Hepatitis C 62 0.028
396
ORL011 Oral Cancer 62 0.028
397
P ANP001 Anaplastic Large Cell Lymphoma 62 0.028
398
THY121 Thyroid Gland Anaplastic Carcinoma 62 0.028
399
GRG001 Greig Cephalopolysyndactyly Syndrome 61 0.028
400
CRB011 Cerebrotendinous Xanthomatosis 61 0.028
401
P ART023 Arthropathy 61 0.028
402
CTN007 Cutaneous Leishmaniasis 61 0.028
403
ACQ007 Acquired Immunodeficiency Syndrome 61 0.028
405
P TXP001 Toxoplasmosis 61 0.028
406
THR100 Thrombocytopenic Purpura, Autoimmune 61 0.028
407
VTR013 Vitreoretinopathy, Neovascular Inflammatory 61 0.028
408
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 61 0.028
409
P PNL012 Penile Cancer 61 0.028
410
P VNT002 Ventricular Septal Defect 61 0.028
411
P CHR285 Chronic Myelomonocytic Leukemia 60 0.028
412
PPT005 Peptic Ulcer Disease 60 0.028
413
P KDN017 Kidney Cancer 60 0.028
414
WLL001 Williams-Beuren Syndrome 60 0.028
415
INS001 Insulinoma 60 0.028
416
INT002 Intermittent Claudication 60 0.028
417
PLM033 Pulmonary Embolism 60 0.028
418
BRN002 Bronchiolitis 60 0.028
419
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.028
420
P CRN300 Coronary Heart Disease 1 59 0.028
421
P GLY013 Glycogen Storage Disease 59 0.028
422
DNG002 Dengue Hemorrhagic Fever 59 0.028
423
ANG020 Angiosarcoma 59 0.028
424
IRN001 Iron Deficiency Anemia 59 0.028
425
P MTR012 Mitral Valve Disease 59 0.028
426
c MST023 Mesothelioma, Malignant 59 0.028
427
P UVT001 Uveitis 58 0.028
428
P PLY011 Polycystic Ovary Syndrome 58 0.028
429
EXT034 Extrinsic Allergic Alveolitis 58 0.028
430
TRD006 Tardive Dyskinesia 58 0.028
431
HYD002 Hydronephrosis 58 0.028
432
ERY051 Erythroleukemia, Familial 58 0.028
433
P PYL005 Pyelonephritis 58 0.028
434
P SLP005 Sleep Disorder 58 0.028
435
GLB001 Gilbert Syndrome 58 0.028
436
TNS005 Tonsillitis 58 0.028
437
c THY109 Thyroid Cancer, Nonmedullary, 1 58 0.028
438
P DNG005 Dengue Virus 57 0.028
439
EMB004 Embryonal Carcinoma 57 0.028
440
RHM027 Rheumatic Disease 56 0.028
441
PRP030 Purpura 56 0.028
442
CRH005 Crohn's Colitis 56 0.028
443
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.028
444
c CNT035 Central Nervous System Disease 56 0.028
445
P FTL001 Fetal Alcohol Syndrome 56 0.028
446
MCS002 Mucositis 56 0.028
447
PPL022 Papilloma 56 0.028
448
RHM001 Rheumatic Fever 56 0.028
449
HRT012 Heart Valve Disease 56 0.028
450
MST005 Mastitis 55 0.028
451
ADN027 Adenomyosis 55 0.028
452
P TRM003 Tremor 55 0.028
453
PRN019 Perinatal Necrotizing Enterocolitis 55 0.028
454
THY124 Thyroid Gland Papillary Carcinoma 54 0.028
455
RHM028 Rheumatic Heart Disease 54 0.028
456
OVR059 Ovary Adenocarcinoma 54 0.028
457
P EPD016 Epidermolysis Bullosa 54 0.028
458
LYS003 Lysinuric Protein Intolerance 54 0.028
459
CCC001 Coccidioidomycosis 54 0.028
460
TLN003 Telangiectasis 53 0.028
461
CHR100 Chronic Ulcer of Skin 53 0.028
462
PNM001 Pneumocystosis 53 0.028
463
HLL004 Hellp Syndrome 53 0.028
464
c ACT134 Acute Liver Failure 53 0.028
465
OCL069 Ocular Motor Apraxia 53 0.028
466
P HMC002 Homocystinuria 52 0.028
467
P THY032 Thyroiditis 52 0.028
468
CRV040 Cervix Carcinoma 52 0.028
469
ACR014 Acral Lentiginous Melanoma 52 0.028
470
P TRT010 Teratoma 52 0.028
471
MCL006 Macular Retinal Edema 52 0.028
472
KRT009 Keratosis 52 0.028
473
P CHR345 Chronic Pain 52 0.028
474
GNG012 Gingival Overgrowth 52 0.028
475
P MYT002 Myotonic Dystrophy 52 0.028
476
P RNL017 Renal Oncocytoma 52 0.028
477
HRT011 Heart Septal Defect 52 0.028
478
NPH018 Nephrogenic Systemic Fibrosis 51 0.028
479
RST011 Restrictive Dermopathy, Lethal 51 0.028
480
c NNS007 Nonsyndromic Deafness 51 0.028
481
FML063 Familial Glucocorticoid Deficiency 51 0.028
482
IRK001 Irak4 Deficiency 51 0.028
483
ENT011 Enterocolitis 51 0.028
484
BNN003 Bone Inflammation Disease 51 0.028
485
CRY003 Cryptosporidiosis 50 0.028
486
URM002 Uremia 50 0.028
487
P DDN001 Duodenal Ulcer 50 0.028
488
PLM014 Pleomorphic Adenoma 50 0.028
489
ACH005 Achalasia 50 0.028
490
CRT013 Carotid Stenosis 50 0.028
491
P PLY180 Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy 1 50 0.028
492
c SPN291 Spinocerebellar Ataxia 7 49 0.028
493
CRN030 Coronary Stenosis 49 0.028
494
EPD006 Epidermolysis Bullosa Acquisita 49 0.028
495
HYP006 Hypertensive Heart Disease 49 0.028
496
c MTR002 Mitral Valve Insufficiency 49 0.028
497
P RNV001 Renovascular Hypertension 49 0.028
498
P ATR005 Atrophic Gastritis 49 0.028
499
DGN001 Degenerative Disc Disease 49 0.028
500
P ART106 Arterial Calcification, Generalized, of Infancy, 1 49 0.028
501
GYN001 Gynecomastia 49 0.028
502
NNT012 Neonatal Jaundice 48 0.028
503
ATN005 Autonomic Dysfunction 48 0.028
504
FBR032 Fibromuscular Dysplasia 48 0.028
505
CCN002 Cocaine Abuse 48 0.028
506
XNT003 Xanthomatosis 48 0.028
507
PLP001 Pulpitis 48 0.028
508
HYP068 Hyperostosis 48 0.028
509
PLM035 Pulmonary Eosinophilia 47 0.028
510
SLP001 Sleeping Sickness 47 0.028
511
CHR074 Choriocarcinoma 47 0.028
512
PPT001 Peptic Esophagitis 47 0.028
513
NCR007 Necrotizing Fasciitis 47 0.028
514
P BNG032 Benign Mesothelioma 47 0.028
515
HDN002 Head Injury 47 0.028
516
FSC004 Fasciitis 47 0.028
517
P RNL015 Renal Hypertension 47 0.028
518
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 47 0.028
519
PRP007 Priapism 47 0.028
520
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 47 0.028
521
c MLG069 Malignant Hypertension 46 0.028
522
HMP009 Haemophilus Influenzae 46 0.028
523
PSD009 Pseudohermaphroditism 46 0.028
524
c OPT051 Opitz Gbbb Syndrome, Type I 46 0.028
525
c ATM099 Autoimmune Uveitis 45 0.028
526
PRX001 Peroxisomal Disease 45 0.028
527
PNM013 Pneumococcal Meningitis 45 0.028
528
ART031 Aortic Coarctation 45 0.028
529
c ACT076 Acute Myocarditis 45 0.028
530
SPN119 Spondylarthropathy 45 0.028
531
c FTL006 Fetal Alcohol Spectrum Disorder 45 0.028
532
ASP026 Asplenia, Isolated Congenital 45 0.028
533
CYN002 Cyanosis, Transient Neonatal 45 0.028
534
KHN001 Kuhnt-Junius Degeneration 45 0.028
535
PDT035 Pediatric Systemic Lupus Erythematosus 45 0.028
536
TLR001 Tularemia 44 0.028
537
SPH001 Sapho Syndrome 44 0.028
538
ORL015 Oral Squamous Cell Carcinoma 44 0.028
539
MTC004 Mitochondrial Encephalomyopathy 44 0.028
540
HYP457 Hypertrophic Scars 44 0.028
541
ANT003 Antley-Bixler Syndrome 43 0.028
542
SGN002 Signet Ring Cell Adenocarcinoma 43 0.028
543
P AVS003 Avascular Necrosis 43 0.028
544
c MLG079 Malignant Pleural Mesothelioma 43 0.028
545
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.028
546
ACT003 Acute Kidney Tubular Necrosis 42 0.028
547
CHR466 Chronic Thromboembolic Pulmonary Hypertension 41 0.028
548
OCL052 Ocular Dominance 41 0.028
549
P TRC031 Trichorhinophalangeal Syndrome 41 0.028
550
ARB001 Ariboflavinosis 41 0.028
551
CRB086 Cerebral Aneurysms 41 0.028
552
KLD004 Keloid Disorder 41 0.028
553
DRG002 Drug-Induced Hepatitis 41 0.028
554
HYP026 Hypoglycemic Coma 41 0.028
555
PRM329 Premature Aging 41 0.028
556
c TRC022 Tricuspid Valve Insufficiency 41 0.028
557
PLY100 Polyploidy 41 0.028
558
OST006 Osteoblastoma 40 0.028
559
MST004 Mast Cell Neoplasm 40 0.028
561
LCH001 Leech Infestation 40 0.028
562
OVR094 Ovarian Epithelial Cancer 39 0.028
563
CDQ001 Cauda Equina Syndrome 39 0.028
564
P ALK015 Alk-Positive Anaplastic Large Cell Lymphoma 39 0.028
565
CHL147 Chlamydia Pneumonia 39 0.028
566
MYC017 Mycobacterium Kansasii 39 0.028
567
AMN006 Aminoaciduria 39 0.028
568
EXT007 Extracutaneous Mastocytoma 39 0.028
569
c RTN143 Retinitis Pigmentosa 47 39 0.028
570
SPS057 Spasticity 38 0.028
571
P CRB059 Cerebellar Degeneration 38 0.028
572
BLR002 Bile Reflux 38 0.028
573
EPT021 Epithelial Recurrent Erosion Dystrophy 38 0.028
574
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 38 0.028
575
STR077 Streptococcal Toxic-Shock Syndrome 38 0.028
576
SYS071 Systemic Autoimmune Disease 38 0.028
577
ACY011 Acyl-Coa Dehydrogenase Deficiency 38 0.028
578
STR103 Streptococcus Pneumonia 37 0.028
579
PNB004 Panbronchiolitis, Diffuse 37 0.028
580
CRT004 Carotid Artery Thrombosis 37 0.028
581
ALC005 Alcoholic Pancreatitis 37 0.028
582
c ATM022 Autoimmune Myocarditis 36 0.028
583
c PRG020 Paragangliomas 3 36 0.028
584
VSM001 Vasomotor Rhinitis 36 0.028
585
HYP114 Hypertensive Nephropathy 36 0.028
586
MTH026 Methemoglobinemia Due to Deficiency of Methemoglobin Reductase 36 0.028
587
CVR010 Cavernous Malformation 36 0.028
588
c LKM004 Leukemia, B-Cell, Chronic 35 0.028
589
GNT167 Genetic Obesity 35 0.028
590
DXR001 Doxorubicin Induced Cardiomyopathy 34 0.028
591
ANT042 Antley-Bixler Syndrome with Genital Anomalies and Disordered Steroidogenesis 34 0.028
593
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.028
594
c NTR047 Neutropenia, Severe Congenital, 1, Autosomal Dominant 34 0.028
595
NRX001 Neuroaxonal Dystrophy 33 0.028
596
INF021 Infant Gynecomastia 32 0.028
598
P MGL010 Megalencephalic Leukoencephalopathy with Subcortical Cysts 2a 31 0.028
599
ECT108 Ectodermal Dysplasia and Immunodeficiency 1 30 0.028
600
MLG163 Malignant Tumor of Penis 30 0.028
601
GLY111 Glycogen Storage Disease Due to Glucose-6-Phosphatase Deficiency Type Ib 30 0.028
602
ARG004 Argyria 28 0.028
603
MGL012 Megaloblastic Anemia Due to Dihydrofolate Reductase Deficiency 28 0.028
604
CYT018 Cytochrome P450 2d6 Variant 28 0.028
605
CTN027 Cutaneous Mastocytoma 27 0.028
606
TXC004 Toxic Diffuse Goiter 27 0.028
607
c RTN140 Retinitis Pigmentosa 67 27 0.028
608
STN013 Stenotrophomonas Maltophilia Infection 26 0.028
609
URT049 Urate Oxidase, Pseudogene 26 0.028
610
c CNG223 Congenital Methemoglobinemia 25 0.028
611
TRY004 Trypanosomiasis, Human East-African 25 0.028
612
MYT026 Myotonia Atrophica 25 0.028
613
CRT066 Cortisone Reductase Deficiency 2 24 0.028
614
P STR035 Streptococcal Group a Invasive Disease 24 0.028
615
c TRN047 Transient Congenital Hypothyroidism 24 0.028
616
CRB087 Cerebral Arteriosclerosis 23 0.028
617
c RNG019 Ring Chromosome 3 22 0.028
618
BRN147 Brain Inflammatory Disease 9 0.028
Content
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