Search results for NADP

582 hits were found for NADP

# Family MCID Name MIFTS Score
1
GLC009 Glucosephosphate Dehydrogenase Deficiency 53 5.935
2
P HML002 Hemolytic Anemia 62 5.347
3
HLX001 Helix Syndrome 48 5.192
4
GLM045 Glioma 63 3.693
5
24D001 2,4-Dienoyl-Coa Reductase Deficiency 34 3.422
6
HYP266 Hypoxia 57 3.401
7
GLL048 Glial Tumor 52 3.356
8
FTT001 Fatty Liver Disease 62 3.240
9
PPL052 Papillomatosis, Confluent and Reticulated 34 3.066
10
ANX004 Anoxia 40 2.978
11
P PLL002 Pellagra 46 2.877
12
GLB002 Glioblastoma 67 2.849
13
HYP066 Hyperglycemia 61 2.827
14
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 50 2.804
15
P MYC084 Mycobacterium Tuberculosis 1 68 2.775
16
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 2.668
17
PRT037 Pertussis 65 2.668
18
NNL005 Non-Alcoholic Fatty Liver Disease 63 2.615
19
PST092 Posttransplant Acute Limbic Encephalitis 28 2.553
20
CHL014 Cholera 62 2.553
21
P HRD144 Hereditary Mixed Polyposis Syndrome 54 2.513
22
MLR004 Malaria 80 2.498
23
P GLM040 Glioma Susceptibility 1 71 2.493
24
MLG169 Malignant Astrocytoma 57 2.430
25
P NRB001 Neuroblastoma 66 2.349
26
HMP009 Haemophilus Influenzae 41 2.349
27
HYP056 Hypoglycemia 65 2.297
28
LPT001 Leptospirosis 66 2.182
29
P TXP001 Toxoplasmosis 60 2.182
30
48X005 48,xyyy 39 2.171
31
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 2.149
32
NNT012 Neonatal Jaundice 53 2.103
33
c LKM061 Leukemia, Acute Myeloid 83 2.079
34
CND006 Candida Glabrata 30 1.981
35
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.962
36
INS001 Insulinoma 59 1.962
37
ATH013 Atherosclerosis Susceptibility 63 1.886
38
GRD001 Giardiasis 46 1.886
39
P CHR012 Chronic Granulomatous Disease 69 1.880
40
CNG017 Congenital Nonspherocytic Hemolytic Anemia 33 1.880
41
47X002 47,xyy 48 1.805
42
ANT024 Anthrax Disease 58 1.805
43
ISC004 Ischemia 61 1.805
44
P CTR002 Cataract 60 1.781
45
P MYC008 Myocarditis 59 1.781
46
APP015 Apparent Mineralocorticoid Excess 57 1.773
47
P TRM004 Trimethylaminuria 45 1.718
48
P CTN015 Cutaneous T Cell Lymphoma 48 1.718
49
P PSR002 Psoriasis 63 1.718
50
PST011 Pustulosis of Palm and Sole 52 1.718
51
HYP005 Hypokalemia 55 1.718
52
QFV001 Q Fever 62 1.718
53
DFC004 Deficiency Anemia 74 1.658
54
P HYP086 Hypothyroidism 69 1.658
55
c DNT047 Dentinogenesis Imperfecta Type 2 35 1.658
56
VLV047 Volvulus of Midgut 52 1.624
57
OCL069 Ocular Motor Apraxia 57 1.624
58
DBT010 Diabetic Neuropathy 54 1.624
59
P MSC005 Muscular Dystrophy 67 1.624
60
P LCT001 Lactic Acidosis 51 1.624
61
CMB083 Combined Immunodeficiency and Megaloblastic Anemia with or Without Hyperhomocysteinemia 28 1.624
62
TXC005 Toxic Shock Syndrome 62 1.624
63
P MLN008 Melanoma 76 1.624
64
SLP001 Sleeping Sickness 56 1.598
66
IRN002 Iron Metabolism Disease 57 1.535
67
P HYP769 Hyperlysinemia, Type I 42 1.519
68
NRR001 Neuroretinitis 42 1.519
69
RTN023 Retinitis 46 1.519
70
c RNG015 Ring Chromosome 2 22 1.519
71
P MYL006 Myeloid Leukemia 61 1.470
72
P BLD134 Bladder Cancer 79 1.402
73
P LNG064 Lung Cancer Susceptibility 3 70 1.402
74
LPD008 Lipid Metabolism Disorder 62 1.402
75
c MCR130 Microvascular Complications of Diabetes 6 41 1.401
76
CMP034 Complete Androgen Insensitivity Syndrome 55 1.401
77
c MCR120 Microvascular Complications of Diabetes 7 47 1.401
78
PYR009 Pyridoxine Deficiency Anemia 35 1.401
79
RCK004 Rickets 68 1.401
80
c MCR113 Microvascular Complications of Diabetes 3 52 1.401
81
c MCR133 Microvascular Complications of Diabetes 4 41 1.401
82
HGH043 High Grade Glioma 45 1.401
83
P URT039 Urticaria 58 1.401
84
HYP026 Hypoglycemic Coma 37 1.401
85
END057 Endometrial Cancer 72 1.330
86
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 1.330
87
DPH001 Diphtheria 59 1.330
88
HYP060 Hyperinsulinism 54 1.330
89
MSC157 Muscular Dystrophy, Duchenne Type 79 1.260
90
c CHR708 Chronic Urticaria 42 1.260
91
P RTN016 Retinal Degeneration 52 1.260
92
HMS001 Hemosiderosis 48 1.260
93
ANP005 Anaplastic Astrocytoma 57 1.260
94
DRM006 Dermatitis 62 1.260
95
P HYP265 Hypotonia 42 1.260
96
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.254
97
MTB004 Metabolic Acidosis 48 1.254
98
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 1.254
99
P BCL017 B-Cell Lymphoma 59 1.254
100
CHG001 Chagas Disease 66 1.254
101
BLR008 Bilirubin Metabolic Disorder 57 1.254
102
P HYP076 Hyperthyroidism 53 1.254
103
P SCK005 Sickle Cell Disease 56 1.254
104
AGN016 Aging 54 1.173
105
P OVR042 Ovarian Cancer 88 1.173
106
P PNC035 Pancreatic Cancer 86 1.173
107
OST159 Osteogenic Sarcoma 66 1.173
108
PNC129 Pancreatic Adenocarcinoma 65 1.173
109
TRY001 Trypanosomiasis 50 1.173
110
P LKM002 Leukemia 67 1.173
111
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.173
112
BRN071 Brain Injury 50 1.173
113
P ATX030 Ataxia-Telangiectasia 80 1.086
114
DFF005 Diffuse Large B-Cell Lymphoma 54 1.086
115
LKC009 Leukocyte Adhesion Deficiency, Type I 70 1.086
116
P GST053 Gastric Cancer 83 1.086
117
P HPT023 Hepatocellular Carcinoma 96 1.086
118
CHL065 Cholangiocarcinoma 58 1.086
119
THY029 Thyroid Carcinoma 51 1.086
120
P MYP004 Myopathy 67 1.086
121
P OLG002 Oligodendroglioma 66 1.086
122
P PLM036 Pulmonary Fibrosis 66 1.086
123
TLN003 Telangiectasis 51 1.086
124
P ADN016 Adenocarcinoma 63 1.086
125
INT079 Intrahepatic Cholangiocarcinoma 51 1.086
126
P OVR046 Ovarian Cyst 46 1.086
127
P ENC018 Encephalopathy 62 1.086
128
DWR001 Dwarfism 44 1.086
129
P CRC039 Coarctation of Aorta 46 1.076
130
DVR002 Diverticulitis 46 1.076
131
P RRH023 Rare Hereditary Hemochromatosis 54 1.076
132
PLM001 Pulmonary Tuberculosis 69 1.076
133
VCC001 Vaccinia 47 1.076
134
ADN018 Adenoma 59 1.076
135
CCC002 Coccidiosis 50 1.076
136
CLN015 Colon Adenocarcinoma 65 1.076
137
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.991
138
c ATR087 Atrial Standstill 1 74 0.991
139
P CLR023 Colorectal Cancer 100 0.991
140
NNL006 Non-Alcoholic Steatohepatitis 54 0.991
141
NRL016 Neural Tube Defects 81 0.991
142
RNL114 Renal Cell Carcinoma, Nonpapillary 80 0.991
143
BCT022 Bacterial Infectious Disease 56 0.991
144
TRM010 Traumatic Brain Injury 51 0.991
145
CHR074 Choriocarcinoma 46 0.991
146
P LVR013 Liver Disease 69 0.991
147
P FBR017 Fibrosarcoma 56 0.991
148
P BRS044 Breast Adenocarcinoma 58 0.991
149
BLD131 Bladder Urothelial Carcinoma 60 0.991
150
PRT036 Peritonitis 65 0.991
151
P BRB001 Beriberi 44 0.991
152
P HRT032 Heart Disease 81 0.991
153
PRS045 Prostatic Hypertrophy 53 0.991
154
TRC008 Trachoma 53 0.991
155
P BNG032 Benign Mesothelioma 53 0.991
156
P GLM007 Glomerulonephritis 60 0.991
157
CRT066 Cortisone Reductase Deficiency 2 23 0.940
158
PRS129 Prostatic Hyperplasia, Benign 49 0.886
159
SPP011 Suppression of Tumorigenicity 12 61 0.886
160
P RTN008 Retinitis Pigmentosa 80 0.886
161
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.886
162
BTN004 Biotin Deficiency 45 0.886
163
CLT003 Colitis 63 0.886
164
BRN032 Brain Glioma 45 0.886
165
c HYP602 Hyperoxaluria, Primary, Type Ii 49 0.886
166
c HYP836 Hypercholesterolemia, Familial, 1 73 0.886
167
ESP021 Esophageal Cancer 83 0.886
168
HRW001 Hair Whorl 35 0.886
169
ORG002 Organic Acidemia 44 0.886
170
SKN019 Skin Melanoma 71 0.886
171
DGN001 Degenerative Disc Disease 49 0.886
172
ALL006 Allergic Asthma 56 0.886
173
CRV038 Cervical Squamous Cell Carcinoma 58 0.886
174
LNG039 Lung Squamous Cell Carcinoma 57 0.886
175
CHL045 Choline Deficiency Disease 39 0.886
176
c PRC016 Pre-Eclampsia 65 0.886
177
GTR002 Goiter 53 0.886
178
DYS015 Dysentery 50 0.886
179
PRS021 Prostatic Adenoma 43 0.886
180
UTR056 Uterine Corpus Endometrial Carcinoma 27 0.886
181
END075 Endocervical Adenocarcinoma 37 0.886
182
P PYL005 Pyelonephritis 57 0.886
183
P PRM002 Primary Hyperoxaluria 65 0.886
184
NRD001 Neurodermatitis 39 0.886
185
RFR010 Refractory Anemia 49 0.768
186
P CRN300 Coronary Heart Disease 1 73 0.768
187
P RHM011 Rheumatoid Arthritis 82 0.768
188
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.768
189
DGL002 D-Glyceric Aciduria 41 0.768
190
P PLM037 Pulmonary Hypertension 72 0.768
191
c MCR115 Microvascular Complications of Diabetes 5 65 0.768
192
MYL009 Myelodysplastic Syndrome 67 0.768
193
MSC007 Muscle Hypertrophy 64 0.768
194
c 2HY001 2-Hydroxyglutaric Aciduria 38 0.768
195
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 0.768
196
c PCH010 Pachyonychia Congenita 3 43 0.768
197
FRC001 Fructose-1,6-Bisphosphatase Deficiency 50 0.768
198
P GLC113 Galactosemia I 66 0.768
199
MYL005 Myelofibrosis 71 0.768
200
P SPP010 Suppressor of Tumorigenicity 3 51 0.768
201
P SRC025 Sarcoidosis 1 71 0.768
202
PYR041 Pyruvate Kinase Deficiency of Red Cells 57 0.768
203
URT049 Urate Oxidase, Pseudogene 24 0.768
204
c HYP595 Hypertension, Essential 85 0.768
205
c TYP009 Type 2 Diabetes Mellitus 92 0.768
206
MLD001 Melioidosis 67 0.768
207
GLC003 Glucose Intolerance 54 0.768
208
c RTN130 Retinitis Pigmentosa 46 40 0.768
209
FML063 Familial Glucocorticoid Deficiency 58 0.768
210
ACT003 Acute Kidney Tubular Necrosis 46 0.768
211
P NRP001 Neuropathy 60 0.768
212
P DBT009 Diabetes Mellitus 67 0.768
213
ULC004 Ulcerative Colitis 74 0.768
214
FDL002 Food Allergy 47 0.768
215
P EPL164 Epilepsy 68 0.768
216
P SKN015 Skin Carcinoma 71 0.768
217
GST040 Gastric Adenocarcinoma 67 0.768
218
P ART022 Arthritis 71 0.768
219
P PRD008 Periodontitis 64 0.768
220
CRB004 Cerebral Artery Occlusion 45 0.768
221
P LTR001 Lateral Sclerosis 58 0.768
222
c ACT027 Acute Pancreatitis 60 0.768
223
P ECL001 Eclampsia 52 0.768
224
TXC004 Toxic Diffuse Goiter 23 0.768
225
ORN001 Ornithosis 39 0.768
226
c CNG027 Congenital Hemolytic Anemia 48 0.768
227
P PNC044 Pancreatitis 61 0.768
228
P PRP019 Peripheral Nervous System Disease 58 0.768
229
DBT007 Diabetic Cataract 36 0.768
230
CHL068 Cholestasis 61 0.768
231
P CRD246 Cardiovascular System Disease 56 0.768
232
SQM006 Squamous Cell Carcinoma 60 0.768
233
CLP006 Clopidogrel Resistance 44 0.768
234
CRL001 Cerulean Cataract 26 0.768
235
BRN056 Bronchopulmonary Dysplasia 56 0.768
236
MYX004 Myxedema 43 0.633
237
CRN036 Craniopharyngioma 64 0.633
238
c BSL007 Basal Cell Carcinoma 68 0.633
239
SNL007 Senile Cataract 40 0.633
240
FRC013 Fructose Utilization 15 0.627
241
P SMP003 Simpson-Golabi-Behmel Syndrome 49 0.627
242
PLY100 Polyploidy 36 0.627
243
STN013 Stenotrophomonas Maltophilia Infection 26 0.627
244
P ALZ034 Alzheimer Disease 87 0.627
245
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.627
246
c GLL024 Gallbladder Disease 1 52 0.627
247
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.627
248
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.627
249
ASP030 Aspirin Resistance 40 0.627
250
P KLZ004 Kala-Azar 1 41 0.627
251
c PLM164 Pulmonary Hypertension, Primary, 1 76 0.627
252
P PRK057 Parkinson Disease, Late-Onset 80 0.627
253
c L2H001 L-2-Hydroxyglutaric Aciduria 49 0.627
254
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.627
255
P INF037 Inflammatory Bowel Disease 53 0.627
256
P PLY014 Polycystic Kidney Disease 69 0.627
257
LWG006 Low Grade Glioma 41 0.627
258
BNR002 Bone Resorption Disease 47 0.627
259
P LYM118 Lymphoma 67 0.627
260
P SML001 Small Cell Carcinoma 52 0.627
261
URL001 Urolithiasis 46 0.627
262
P CHN012 Chondrosarcoma 57 0.627
263
P FRD001 Friedreich Ataxia 61 0.627
264
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.627
265
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.627
266
c BRN108 Branchiootic Syndrome 1 62 0.627
268
P MCR129 Microvascular Complications of Diabetes 1 68 0.627
269
MYP071 Myopathy Due to Myoadenylate Deaminase Deficiency 43 0.627
270
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.627
271
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.627
272
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.627
273
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.627
274
DWN001 Down Syndrome 70 0.627
275
P RTN024 Retinoblastoma 73 0.627
276
FND001 Fundus Albipunctatus 55 0.627
277
P HNT016 Huntington Disease 73 0.627
278
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.627
279
P MYC007 Myocardial Infarction 70 0.627
280
RBF001 Riboflavin Deficiency 49 0.627
281
MNN043 Meningioma, Familial 79 0.627
282
DSS032 Disease by Infectious Agent 55 0.627
283
CLR109 Colorectal Adenocarcinoma 50 0.627
284
ARG004 Argyria 26 0.627
285
PRM329 Premature Aging 36 0.627
286
RFR009 Refractory Cytopenia with Multilineage Dysplasia 30 0.627
287
ANG046 Angioimmunoblastic T-Cell Lymphoma 51 0.627
288
c ACT073 Acute Leukemia 58 0.627
289
P OPN001 Open-Angle Glaucoma 55 0.627
290
CNG393 Congenital Muscular Dystrophy with Hyperlaxity 12 0.627
291
CRH001 Crohn's Disease 80 0.627
292
c CHR684 Chronic Kidney Disease 69 0.627
293
CRC021 Carcinosarcoma 64 0.627
294
P LCH002 Lichen Planus 54 0.627
295
RSC001 Rosacea 55 0.627
296
INT040 Intrinsic Asthma 36 0.627
297
P HRP006 Herpes Simplex 65 0.627
298
LSH001 Leishmaniasis 64 0.627
299
GST010 Gestational Trophoblastic Neoplasm 52 0.627
300
HGH041 High-Grade Astrocytoma 36 0.627
301
ACT168 Acute Annular Outer Retinopathy 10 0.627
302
SKN016 Skin Disease 63 0.627
303
P OPT006 Optic Nerve Disease 58 0.627
304
P OLV001 Olivopontocerebellar Atrophy 51 0.627
305
P GST044 Gastritis 55 0.627
306
ART016 Aortic Aneurysm 68 0.627
307
P ACN011 Acne 57 0.627
308
CLR030 Clear Cell Renal Cell Carcinoma 54 0.627
309
P BNG002 Benign Meningioma 36 0.627
310
SCR001 Secretory Meningioma 40 0.627
311
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.627
312
CHL061 Childhood Leukemia 47 0.627
313
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.627
314
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.627
315
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 0.627
316
c MCR112 Microvascular Complications of Diabetes 2 42 0.627
317
GT001 Gout 64 0.627
318
CNN003 Conn's Syndrome 79 0.627
319
ALC006 Alcoholic Hepatitis 61 0.627
320
RYS001 Reye Syndrome 49 0.627
321
KRT009 Keratosis 53 0.627
322
IRN001 Iron Deficiency Anemia 58 0.627
323
P CRD119 Cardiac Arrest 67 0.627
324
CHL123 Chlamydia 58 0.627
325
P PRN023 Prion Disease 60 0.627
326
c INH020 Inherited Metabolic Disorder 48 0.627
327
BRS099 Breast Ductal Carcinoma 61 0.627
328
P ART021 Arteriosclerosis 54 0.627
329
P PLY019 Polyneuropathy 52 0.627
330
DBT002 Diabetic Autonomic Neuropathy 41 0.627
331
SPN021 Spinal Meningioma 50 0.627
332
TLR001 Tularemia 56 0.627
333
HST011 Histoplasmosis 55 0.627
334
P ICH004 Ichthyosis 56 0.627
335
STM007 Stomatitis 54 0.627
337
ANR040 Aneurysm 61 0.627
338
ALL014 Allergic Encephalomyelitis 34 0.627
339
P SPN237 Spina Bifida Aperta 19 0.443
340
P OTT001 Otitis Externa 42 0.443
341
c BCT007 Bacterial Meningitis 55 0.443
342
PRQ002 Paraquat Poisoning 28 0.443
343
HVY003 Heavy Chain Deposition Disease 17 0.443
344
c INH030 Inherited Retinal Disorder 28 0.443
345
c SPS035 Spastic Paraplegia 29 13 0.443
346
P THL005 Thalassemia 56 0.443
347
c ACT134 Acute Liver Failure 59 0.443
348
P NSP012 Nasopharyngeal Carcinoma 61 0.443
349
MTH071 Methane Production 25 0.443
350
DHY002 Dihydropyrimidine Dehydrogenase Deficiency 57 0.443
351
PHS014 Phosphoglycerate Kinase 1 Deficiency 45 0.443
352
c THY107 Thymoma, Familial 42 0.443
353
TRC120 Tricarboxylic Acid Cycle, Defect of 16 0.443
354
LSC001 Lesch-Nyhan Syndrome 62 0.443
355
MST021 Meester-Loeys Syndrome 42 0.443
356
P WSK001 Wiskott-Aldrich Syndrome 72 0.443
357
P LPR021 Leprosy 3 71 0.443
358
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.443
359
ANN002 Anencephaly 57 0.443
360
P AST005 Asthma 76 0.443
361
c PRK090 Parkinson Disease 3, Autosomal Dominant 38 0.443
362
ONC007 Oncocytoma 50 0.443
363
P D2H002 D-2-Hydroxyglutaric Aciduria 1 52 0.443
364
HMC014 Homocysteinemia 52 0.443
365
CRV035 Cervical Cancer 73 0.443
366
ANX010 Anxiety 70 0.443
367
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.443
368
P SCH015 Schizophrenia 74 0.443
369
HRD029 Hereditary Leiomyomatosis and Renal Cell Cancer 56 0.443
370
P PHC003 Pheochromocytoma 69 0.443
371
P LKM071 Leukemia, Chronic Lymphocytic 75 0.443
372
c TBL031 Tubulointerstitial Kidney Disease, Autosomal Dominant, 1 47 0.443
373
CLF027 Cleft Palate, Isolated 64 0.443
374
CRT072 Creutzfeldt-Jakob Disease 68 0.443
375
ATM095 Autoimmune Disease 61 0.443
376
P BRS047 Breast Cancer 98 0.443
377
ALC007 Alcohol Dependence 66 0.443
378
c MST023 Mesothelioma, Malignant 56 0.443
379
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.443
380
c MGR028 Migraine with or Without Aura 1 64 0.443
381
OTT002 Otitis Media 71 0.443
382
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 59 0.443
383
CYS001 Cystic Fibrosis 78 0.443
384
P HYP605 Hyperphenylalaninemia, Bh4-Deficient, B 44 0.443
385
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.443
386
P APL001 Aplastic Anemia 73 0.443
388
P FML011 Familial Adenomatous Polyposis 71 0.443
389
P EXN002 Exanthem 58 0.443
390
HYP001 Hypochromic Microcytic Anemia 37 0.443
391
FML037 Female Breast Cancer 51 0.443
392
ATS010 Autosomal Recessive Disease 42 0.443
393
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.443
394
c D2H003 D-2-Hydroxyglutaric Aciduria 2 35 0.443
395
c BTT014 Beta-Thalassemia 72 0.443
396
P PRK101 Parkinsonism-Dystonia, Infantile, 1 40 0.443
397
P FST017 Fasting Plasma Glucose Level Quantitative Trait Locus 5 12 0.443
398
CYN002 Cyanosis, Transient Neonatal 43 0.443
399
KSH001 Keshan Disease 34 0.443
400
KSH004 Kashin-Beck Disease 38 0.443
401
P HYP111 Hyperprolinemia 45 0.443
402
CVD001 Covid-19 57 0.443
403
ACT098 Acute Erythroid Leukemia 55 0.443
404
P URN019 Urinary Tract Infection 49 0.443
405
MYL020 Myelomeningocele 51 0.443
406
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.443
407
CRH005 Crohn's Colitis 53 0.443
408
HYP025 Hyperphosphatemia 48 0.443
409
c PRM032 Primary Congenital Glaucoma 41 0.443
410
P FTL001 Fetal Alcohol Syndrome 55 0.443
411
CLR108 Colorectal Adenoma 64 0.443
412
HLC007 Helicobacter Pylori Infection 67 0.443
413
c MCR245 Microphthalmia, Syndromic 8 46 0.443
414
c BRT028 Brittle Cornea Syndrome 1 39 0.443
415
IMM167 Immune Deficiency Disease 78 0.443
416
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.443
417
GRG001 Greig Cephalopolysyndactyly Syndrome 64 0.443
418
PRP001 Propionic Acidemia 65 0.443
419
P LKM062 Leukemia, Acute Lymphoblastic 69 0.443
420
c NPH068 Nephronophthisis 16 43 0.443
421
P STN012 Sting-Associated Vasculopathy, Infantile-Onset 42 0.443
422
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 0.443
423
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.443
424
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 55 0.443
425
c DFN134 Deafness, Autosomal Dominant 40 22 0.443
426
c DFN360 Deafness, Autosomal Dominant 69 34 0.443
427
HMM004 Hamamy Syndrome 39 0.443
428
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.443
429
c GLC079 Glaucoma 1, Open Angle, P 23 0.443
430
P MPL001 Maple Syrup Urine Disease 70 0.443
432
BLD065 Blue Diaper Syndrome 20 0.443
433
HRT031 Hartnup Disorder 52 0.443
434
HMC042 Homocystinuria-Megaloblastic Anemia, Cble Complementation Type 33 0.443
435
HYD030 Hydroxykynureninuria 27 0.443
436
c PRD040 Periodontitis, Chronic 52 0.443
437
PHN003 Phenylketonuria 76 0.443
438
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.443
439
GLB001 Gilbert Syndrome 53 0.443
440
P HYP750 Hypertriglyceridemia, Familial 62 0.443
441
P MDL005 Medulloblastoma 75 0.443
442
c HYP731 Hyperaldosteronism, Familial, Type I 58 0.443
443
c SPS094 Spastic Paraplegia 29, Autosomal Dominant 28 0.443
444
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 51 0.443
445
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 53 0.443
446
c HYP807 Hyperinsulinemic Hypoglycemia, Familial, 6 52 0.443
447
c NMN014 Niemann-Pick Disease, Type C2 49 0.443
448
ADR040 Adrenal Gland Pheochromocytoma 46 0.443
449
RNL077 Renal Fibrosis 46 0.443
450
ATS251 Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna 38 0.443
451
CRT020 Cortisone Reductase Deficiency 34 0.443
452
STN011 Sting-Associated Vasculopathy with Onset in Infancy 45 0.443
453
LBR036 Leber Plus Disease 66 0.443
454
ICH054 Ichthyosis, X-Linked 52 0.443
455
c ATS013 Autosomal Recessive Congenital Ichthyosis 66 0.443
456
FCL090 Facial Cleft 30 0.443
457
RPD005 Rapidly Involuting Congenital Hemangioma 46 0.443
458
P ZLL001 Zellweger Syndrome 65 0.443
459
P MSC003 Muscular Atrophy 52 0.443
460
PLM014 Pleomorphic Adenoma 51 0.443
461
MCP006 Mucoepidermoid Carcinoma 48 0.443
462
EXT007 Extracutaneous Mastocytoma 38 0.443
463
PRS042 Prostate Disease 42 0.443
464
SCR011 Scrapie 39 0.443
465
URT010 Ureteral Obstruction 45 0.443
466
VSC003 Visceral Leishmaniasis 55 0.443
467
P HMC002 Homocystinuria 53 0.443
468
CLF001 Cleft Lip 53 0.443
469
P ATR005 Atrophic Gastritis 50 0.443
470
AMB001 Amebiasis 57 0.443
471
VRL011 Viral Infectious Disease 61 0.443
472
P MLG056 Malignant Hyperthermia 66 0.443
473
CHC001 Chickenpox 57 0.443
474
LPD009 Lipid Storage Disease 45 0.443
475
FND002 Fundus Dystrophy 55 0.443
476
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 0.443
477
ACT162 Acute Sensory Ataxic Neuropathy 24 0.443
478
P HYP098 Hypereosinophilic Syndrome 66 0.443
479
P MTH008 Methylmalonic Acidemia 52 0.443
480
P CYS018 Cystitis 59 0.443
481
MST004 Mast Cell Neoplasm 42 0.443
482
c VRL010 Viral Hepatitis 53 0.443
483
TRC003 Trichomoniasis 53 0.443
484
TRT001 Teratocarcinoma 42 0.443
485
P CND004 Candidiasis 58 0.443
486
LNG031 Lung Benign Neoplasm 51 0.443
487
P SYS005 Systemic Scleroderma 74 0.443
488
ADR005 Adrenal Carcinoma 62 0.443
489
P RNL017 Renal Oncocytoma 54 0.443
490
ACQ007 Acquired Immunodeficiency Syndrome 59 0.443
491
P INF038 Influenza 68 0.443
492
NRM005 Neuromuscular Disease 63 0.443
493
PPT005 Peptic Ulcer Disease 58 0.443
494
EBL001 Ebola Hemorrhagic Fever 56 0.443
495
P PLC011 Pilocytic Astrocytoma 57 0.443
496
P MNC007 Monocytic Leukemia 47 0.443
498
VSL013 Visual Impairment and Progressive Phthisis Bulbi 36 0.443
499
P SNS001 Sensorineural Hearing Loss 59 0.443
500
THY006 Thymus Lymphoma 27 0.443
501
LGN002 Legionellosis 62 0.443
502
P DMN002 Dementia 66 0.443
503
P HYP061 Hypertrophic Cardiomyopathy 69 0.443
504
ALL029 Allergic Disease 59 0.443
505
VRC001 Varicocele 48 0.443
506
FLR001 Filarial Elephantiasis 59 0.443
507
PRN009 Paranoid Schizophrenia 49 0.443
508
PRM236 Primary Biliary Cholangitis 60 0.443
509
c ACT068 Acute Cystitis 61 0.443
510
SCK001 Sick Building Syndrome 33 0.443
511
P VSC007 Vascular Disease 63 0.443
512
SNS003 Sensory Peripheral Neuropathy 52 0.443
513
P DDN001 Duodenal Ulcer 53 0.443
514
P NMN002 Niemann-Pick Disease 60 0.443
515
P NPH005 Nephronophthisis 56 0.443
516
P GCH001 Gaucher's Disease 70 0.443
517
DRG002 Drug-Induced Hepatitis 42 0.443
518
P KRN004 Kernicterus 46 0.443
519
TST014 Testicular Cancer 52 0.443
520
ACT078 Acute Porphyria 49 0.443
521
MGL001 Megaloblastic Anemia 58 0.443
522
SCH014 Schistosomiasis 56 0.443
523
PRS036 Parasitic Protozoa Infectious Disease 44 0.443
524
GST033 Gestational Diabetes 61 0.443
525
P RNL015 Renal Hypertension 45 0.443
526
FLR002 Filariasis 55 0.443
527
P HYD006 Hydrocephalus 61 0.443
528
NPH010 Nephrosclerosis 50 0.443
529
ONC002 Onchocerciasis 51 0.443
530
P HYP024 Hypoparathyroidism 55 0.443
531
MCR018 Microcytic Anemia 47 0.443
532
CNG034 Congestive Heart Failure 69 0.443
533
RCT015 Reactive Arthritis 61 0.443
534
LMY003 Leiomyomatosis 44 0.443
535
P INF032 Infertility 57 0.443
536
P SLP005 Sleep Disorder 61 0.443
537
P PNM007 Pneumonia 67 0.443
538
INT020 Intravenous Leiomyomatosis 36 0.443
539
CRT015 Carotid Artery Occlusion 45 0.443
540
PLM029 Palmoplantar Keratosis 48 0.443
541
P CYS039 Cystic Kidney Disease 53 0.443
542
P THY023 Thymoma 64 0.443
543
PSD007 Pseudomyxoma Peritonei 53 0.443
544
P TMP001 Temporal Lobe Epilepsy 49 0.443
545
c FML021 Familial Hypercholesterolemia 72 0.443
546
MSN003 Mesenteric Vascular Occlusion 24 0.443
547
TYP007 Typhoid Fever 64 0.443
548
P PRP029 Porphyria 60 0.443
549
PLS007 Plasmodium Falciparum Malaria 52 0.443
550
P ADL010 Adult Respiratory Distress Syndrome 71 0.443
551
LST001 Listeriosis 59 0.443
552
CTS002 Cat-Scratch Disease 42 0.443
553
RHM001 Rheumatic Fever 59 0.443
554
LYM021 Lymphadenitis 56 0.443
555
P OVR049 Ovarian Disease 52 0.443
556
LCH001 Leech Infestation 38 0.443
557
CHR073 Choreatic Disease 54 0.443
558
NNT010 Nontoxic Goiter 32 0.443
559
HYP014 Hyperuricemia 51 0.443
560
BBS001 Babesiosis 49 0.443
561
ALB002 Albinism 47 0.443
562
P MNN013 Meningitis 65 0.443
563
c JVN010 Juvenile Rheumatoid Arthritis 66 0.443
564
PRM209 Primary Trimethylaminuria 19 0.443
565
DRG003 Drug Dependence 46 0.443
566
c NNS007 Nonsyndromic Deafness 33 0.443
567
HNS001 Hansen's Disease 32 0.443
568
HYP835 Hypothalamic Obesity 38 0.443
569
PTT041 Pituitary Stalk Interruption Syndrome 54 0.443
570
WLL004 Wallerian Degeneration 38 0.443
571
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 0.443
572
RFC001 Rfc1 Canvas / Spectrum Disorder 5 0.443
574
CYT002 Cytokine Deficiency 43 0.443
575
c CNG216 Congenital Hydrocephalus 53 0.443
576
CHR178 Chromosomal Triplication 34 0.443
577
HVY002 Heavy Metal Poisoning 22 0.443
578
MTH046 Methylmalonic Acidemia Without Homocystinuria 39 0.443
579
OVR094 Ovarian Epithelial Cancer 39 0.443
580
CRC006 Carcinoid Syndrome 55 0.443
581
FST010 Fasting Hypoglycemia 33 0.443
582
GLC039 Glucosephosphate Isomerase Deficiency 17 0.443
Content
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