Search results for glycerol 3-phosphate

787 hits were found for glycerol 3-phosphate

# Family MCID Name MIFTS Score
1
GLY014 Glycerol Kinase Deficiency 48 56.226
2
CHR387 Chromosome Xp21 Deletion Syndrome 37 26.066
3
c ACT071 Acute Kidney Failure 60 18.505
4
NNL005 Non-Alcoholic Fatty Liver Disease 63 14.250
5
P KDN018 Kidney Disease 72 14.210
6
FTT001 Fatty Liver Disease 62 13.384
7
HYP056 Hypoglycemia 65 12.583
8
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 11.890
9
P HYP750 Hypertriglyceridemia, Familial 62 11.707
10
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 11.036
11
RPD005 Rapidly Involuting Congenital Hemangioma 46 10.964
12
HYP060 Hyperinsulinism 54 10.859
13
P MSC005 Muscular Dystrophy 67 10.379
14
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 10.250
15
HYP066 Hyperglycemia 61 9.912
16
HLX001 Helix Syndrome 48 9.607
17
48X005 48,xyyy 39 9.604
18
P MYP004 Myopathy 67 9.205
19
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 9.008
20
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 9.008
21
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 9.008
22
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 9.008
23
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 9.008
24
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 9.008
25
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 9.008
26
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 9.008
27
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 9.008
28
MSC157 Muscular Dystrophy, Duchenne Type 79 8.819
29
SLP001 Sleeping Sickness 56 8.603
30
FRC001 Fructose-1,6-Bisphosphatase Deficiency 50 8.311
31
HYP266 Hypoxia 57 8.181
32
P MNN013 Meningitis 65 8.115
33
P NRB001 Neuroblastoma 66 8.062
34
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 66 7.996
35
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 7.736
36
LPD008 Lipid Metabolism Disorder 62 7.622
37
BRN004 Brain Edema 54 7.566
38
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 7.481
39
GLM045 Glioma 63 7.447
40
GLL048 Glial Tumor 52 7.365
41
OCL069 Ocular Motor Apraxia 57 7.196
42
HMP009 Haemophilus Influenzae 41 7.072
43
INS024 Insulin-Like Growth Factor I 78 7.038
44
P MYC084 Mycobacterium Tuberculosis 1 68 6.925
45
47X002 47,xyy 48 6.913
46
ANX004 Anoxia 40 6.864
47
PRT037 Pertussis 65 6.710
48
TRM010 Traumatic Brain Injury 51 6.700
49
BRN071 Brain Injury 50 6.561
50
CHL068 Cholestasis 61 6.550
51
ALL029 Allergic Disease 59 6.486
52
P DRM053 Dermatitis, Atopic 65 6.441
53
P LVR013 Liver Disease 69 6.339
54
P HRD011 Hereditary Spherocytosis 64 6.281
55
TXC005 Toxic Shock Syndrome 62 6.279
56
c THY056 Thyroid Dyshormonogenesis 3 31 6.239
57
PLY150 Polykaryocytosis Inducer 29 6.227
58
c TYP009 Type 2 Diabetes Mellitus 92 6.217
59
P HNT016 Huntington Disease 73 6.216
60
DRM006 Dermatitis 62 6.159
61
ACT003 Acute Kidney Tubular Necrosis 46 6.092
62
P HYP086 Hypothyroidism 69 6.058
63
CHG001 Chagas Disease 66 6.032
64
P CTR177 Citrullinemia, Type Ii, Adult-Onset 55 6.020
65
c STC015 Stickler Syndrome, Type I 51 5.981
66
GLB002 Glioblastoma 67 5.710
67
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 5.676
68
P HYP076 Hyperthyroidism 53 5.676
69
MTB004 Metabolic Acidosis 48 5.658
70
PPL052 Papillomatosis, Confluent and Reticulated 34 5.564
71
CRB004 Cerebral Artery Occlusion 45 5.508
72
INS001 Insulinoma 59 5.445
73
MLR004 Malaria 80 5.405
74
LVR012 Liver Cirrhosis 63 5.402
75
CYS001 Cystic Fibrosis 78 5.375
76
c BRN108 Branchiootic Syndrome 1 62 5.337
77
GLC003 Glucose Intolerance 54 5.325
78
PST092 Posttransplant Acute Limbic Encephalitis 28 5.304
79
P LCT001 Lactic Acidosis 51 5.292
80
P ENC018 Encephalopathy 62 5.249
81
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 5.205
82
CYT002 Cytokine Deficiency 43 5.200
83
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 5.200
84
IRN002 Iron Metabolism Disease 57 5.170
85
c ATS307 Autosomal Recessive Cerebellar Ataxia 39 5.125
86
HRW001 Hair Whorl 35 5.121
87
P KLZ004 Kala-Azar 1 41 5.113
88
LSH001 Leishmaniasis 64 5.113
89
ATS010 Autosomal Recessive Disease 42 5.081
90
CHL014 Cholera 62 5.022
91
TRY001 Trypanosomiasis 50 4.949
92
P CTR002 Cataract 60 4.918
93
P SNS001 Sensorineural Hearing Loss 59 4.886
94
ISC004 Ischemia 61 4.810
95
NRR001 Neuroretinitis 42 4.755
96
MST005 Mastitis 53 4.715
97
RTN023 Retinitis 46 4.714
98
AGN016 Aging 54 4.622
99
HMN044 Human Immunodeficiency Virus Type 1 78 4.615
100
P PRK057 Parkinson Disease, Late-Onset 80 4.611
101
P HRP006 Herpes Simplex 65 4.609
102
P HDC001 Headache 57 4.540
103
P ALP106 Alport Syndrome 1, X-Linked 47 4.536
104
P BRS047 Breast Cancer 98 4.475
105
P ALZ034 Alzheimer Disease 87 4.433
106
GST033 Gestational Diabetes 61 4.432
107
HDN002 Head Injury 44 4.411
108
LYM017 Lyme Disease 62 4.402
109
VCC001 Vaccinia 47 4.395
110
CTR172 Citrullinemia, Classic 65 4.393
111
c DNT047 Dentinogenesis Imperfecta Type 2 35 4.367
112
ADN018 Adenoma 59 4.339
113
SKN016 Skin Disease 63 4.334
114
c THY071 Thyroid Dyshormonogenesis 1 31 4.322
115
CHL123 Chlamydia 58 4.297
116
P LNG032 Lung Cancer 98 4.281
117
P INF032 Infertility 57 4.281
118
P THL005 Thalassemia 56 4.245
119
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 4.225
120
BCT022 Bacterial Infectious Disease 56 4.198
121
P BRG001 Brugada Syndrome 69 4.194
122
P GST053 Gastric Cancer 83 4.174
123
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 4.167
124
SCH014 Schistosomiasis 56 4.167
125
HGH043 High Grade Glioma 45 4.158
126
KRT019 Keratitis, Hereditary 66 4.146
127
c INH020 Inherited Metabolic Disorder 48 4.132
128
P BLD134 Bladder Cancer 79 4.079
129
AZS001 Azoospermia 45 4.073
130
c MCR115 Microvascular Complications of Diabetes 5 65 4.059
131
c CNG012 Congenital Generalized Lipodystrophy 65 4.029
132
c HYP836 Hypercholesterolemia, Familial, 1 73 4.017
133
NNL006 Non-Alcoholic Steatohepatitis 54 4.006
134
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 3.998
135
P DBT009 Diabetes Mellitus 67 3.945
136
INT323 Intraocular Pressure Quantitative Trait Locus 64 3.936
137
P EYD002 Eye Disease 57 3.920
138
P GLY013 Glycogen Storage Disease 60 3.912
139
SRC014 Sarcoma 65 3.909
140
CND006 Candida Glabrata 30 3.878
141
STM007 Stomatitis 54 3.861
142
c TYP008 Type 1 Diabetes Mellitus 70 3.850
143
PRT251 Proteinuria, Chronic Benign 57 3.837
144
P MLN007 Male Infertility 56 3.815
145
P MYG005 Myoglobinuria 40 3.767
146
c SPR086 Spermatogenic Failure 3 46 3.758
147
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 3.695
148
DFC004 Deficiency Anemia 74 3.681
149
OVR063 Overnutrition 42 3.670
150
c PCH010 Pachyonychia Congenita 3 43 3.663
151
PLM129 Pulmonary Disease, Chronic Obstructive 74 3.644
152
OST159 Osteogenic Sarcoma 66 3.629
153
P HPT021 Hepatitis 69 3.618
154
P CND004 Candidiasis 58 3.609
155
SQM006 Squamous Cell Carcinoma 60 3.596
156
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 41 3.590
157
ARG004 Argyria 26 3.565
158
HYP555 Hypertriglyceridemia, Transient Infantile 38 3.531
159
c BTT014 Beta-Thalassemia 72 3.521
160
P PRD008 Periodontitis 64 3.508
161
BRR012 Berardinelli-Seip Congenital Lipodystrophy 25 3.508
162
HPT004 Hepatic Coma 43 3.504
163
HPT019 Hepatic Encephalopathy 59 3.504
164
P MLT020 Multiple Sclerosis 79 3.487
165
P HYP265 Hypotonia 42 3.466
166
P SZR006 Seizure Disorder 70 3.442
167
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 3.438
168
c GRV008 Graves Disease 1 54 3.421
169
P MLN008 Melanoma 76 3.411
170
ADR022 Adrenomyeloneuropathy 39 3.407
171
ADR007 Adrenoleukodystrophy 73 3.407
172
URT010 Ureteral Obstruction 45 3.398
173
BNR002 Bone Resorption Disease 47 3.371
174
ATH013 Atherosclerosis Susceptibility 63 3.365
175
c ACT068 Acute Cystitis 61 3.346
176
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 3.338
177
P HPT023 Hepatocellular Carcinoma 96 3.309
178
c HYP595 Hypertension, Essential 85 3.298
179
P MSC003 Muscular Atrophy 52 3.291
180
SPN035 Spindle Cell Sarcoma 54 3.290
181
P ALC033 Alcohol Use Disorder 61 3.288
182
P PNC035 Pancreatic Cancer 86 3.265
183
P DNG005 Dengue Virus 56 3.254
184
BRN024 Bronchitis 67 3.247
185
IMM167 Immune Deficiency Disease 78 3.243
186
FST010 Fasting Hypoglycemia 33 3.235
187
P LNG064 Lung Cancer Susceptibility 3 70 3.233
188
P OVR042 Ovarian Cancer 88 3.227
189
P GLM040 Glioma Susceptibility 1 71 3.216
190
MLG169 Malignant Astrocytoma 57 3.216
191
c CHL116 Cholestasis, Intrahepatic, of Pregnancy, 1 52 3.203
192
DWN001 Down Syndrome 70 3.177
193
P NTR004 Neutropenia 63 3.160
194
P CNT004 Centronuclear Myopathy 57 3.145
195
OST012 Osteoarthritis 77 3.134
196
P SLP006 Sleep Apnea 69 3.133
197
c HPT073 Hepatitis C Virus 71 3.121
198
LPT014 Leptin Deficiency or Dysfunction 78 3.119
199
GST045 Gastroenteritis 58 3.111
200
c HPT016 Hepatitis B 62 3.085
201
P PLY014 Polycystic Kidney Disease 69 3.065
202
c PRC016 Pre-Eclampsia 65 3.048
203
P CHR012 Chronic Granulomatous Disease 69 3.041
204
P ART022 Arthritis 71 3.039
205
GTR002 Goiter 53 3.039
206
P CRN300 Coronary Heart Disease 1 73 3.003
207
P PLY011 Polycystic Ovary Syndrome 57 2.996
208
CLT003 Colitis 63 2.993
209
P NRP001 Neuropathy 60 2.977
210
P TRN020 Turner Syndrome 67 2.965
211
PLR005 Pleuropneumonia 33 2.962
212
URM002 Uremia 47 2.961
213
c MJR022 Major Affective Disorder 8 38 2.956
214
c MJR024 Major Affective Disorder 9 41 2.956
215
P BPL003 Bipolar Disorder 56 2.956
216
P VSC007 Vascular Disease 63 2.946
217
P PRK039 Parkinsonism 55 2.935
218
ALC007 Alcohol Dependence 66 2.929
219
THY029 Thyroid Carcinoma 51 2.928
220
P RHN004 Rhinitis 57 2.928
221
ATM095 Autoimmune Disease 61 2.907
222
RLP003 Relapsing Fever 49 2.868
223
RYS001 Reye Syndrome 49 2.863
224
P ACN011 Acne 57 2.850
225
c HPT001 Hepatitis C 62 2.849
226
P INF037 Inflammatory Bowel Disease 53 2.839
227
P HML002 Hemolytic Anemia 62 2.824
228
P PNC044 Pancreatitis 61 2.819
229
ANT024 Anthrax Disease 58 2.794
230
P ENC004 Encephalitis 61 2.789
231
MNN020 Meningococcal Infection 45 2.787
232
c ATR087 Atrial Standstill 1 74 2.783
233
P RHM011 Rheumatoid Arthritis 82 2.775
234
P ASP006 Aspergillosis 72 2.772
235
c SML038 Small Cell Cancer of the Lung 69 2.766
236
VSC003 Visceral Leishmaniasis 55 2.765
237
P PRS040 Prostate Cancer 95 2.761
238
c CHR684 Chronic Kidney Disease 69 2.758
239
P GLM007 Glomerulonephritis 60 2.752
240
ACT098 Acute Erythroid Leukemia 55 2.752
241
P ADN016 Adenocarcinoma 63 2.746
242
P END033 Endocarditis 58 2.734
243
BRK010 Burkitt Lymphoma 66 2.729
244
P AST005 Asthma 76 2.721
245
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 2.719
246
P CHR071 Charcot-Marie-Tooth Disease 64 2.711
247
P CRD119 Cardiac Arrest 67 2.703
248
MDD018 Middle East Respiratory Syndrome 44 2.699
249
PRT036 Peritonitis 65 2.688
250
c ACT027 Acute Pancreatitis 60 2.677
251
STR067 Stroke, Ischemic 80 2.670
252
RNL077 Renal Fibrosis 46 2.668
253
ORL015 Oral Squamous Cell Carcinoma 43 2.668
254
c HPT003 Hepatitis a 63 2.665
255
GRD001 Giardiasis 46 2.665
256
P FBR017 Fibrosarcoma 56 2.650
257
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 2.635
258
TBL029 Tubulin, Beta 28 2.621
259
P ZLL001 Zellweger Syndrome 65 2.612
260
P CLR023 Colorectal Cancer 100 2.606
261
PNC129 Pancreatic Adenocarcinoma 65 2.595
262
c LKM063 Leukemia, Chronic Myeloid 71 2.570
263
ACQ007 Acquired Immunodeficiency Syndrome 59 2.570
264
ART016 Aortic Aneurysm 68 2.569
265
INF034 Infective Endocarditis 54 2.567
266
P ICH004 Ichthyosis 56 2.567
267
ALB002 Albinism 47 2.554
268
P SPP010 Suppressor of Tumorigenicity 3 51 2.547
269
TCK003 Tick-Borne Relapsing Fever 35 2.544
270
MYC019 Mycobacterium Marinum 29 2.544
271
P SYP003 Syphilis 59 2.532
272
CCC002 Coccidiosis 50 2.524
273
P CLS010 Cluster Headache 42 2.522
274
P DRR001 Diarrhea 55 2.509
275
ANR040 Aneurysm 61 2.508
276
MYL069 Myeloma, Multiple 77 2.504
277
BCT002 Bacterial Vaginosis 53 2.502
278
P ANP001 Anaplastic Large Cell Lymphoma 61 2.492
279
RNL114 Renal Cell Carcinoma, Nonpapillary 80 2.488
280
P MYL006 Myeloid Leukemia 61 2.482
281
P RTN024 Retinoblastoma 73 2.482
282
c DLT002 Dilated Cardiomyopathy 78 2.480
283
LGN006 Legionnaire Disease 52 2.453
284
P RCT021 Rectum Cancer 54 2.442
285
VLV047 Volvulus of Midgut 52 2.436
286
P TRT010 Teratoma 51 2.434
287
SYN036 Syncope 45 2.421
288
IRR002 Irritable Bowel Syndrome 65 2.421
289
KRT002 Keratomalacia 55 2.418
290
c BRG006 Brugada Syndrome 2 31 2.415
291
c VRL010 Viral Hepatitis 53 2.405
292
DBT084 Diabetes Mellitus, Ketosis-Prone 60 2.390
293
TLR001 Tularemia 56 2.389
294
P RTN008 Retinitis Pigmentosa 80 2.386
295
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 2.386
296
SPN186 Spinal Cord Injury 61 2.386
297
c THY107 Thymoma, Familial 42 2.384
298
P THY023 Thymoma 64 2.384
299
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 2.383
300
P PRP019 Peripheral Nervous System Disease 58 2.381
301
BLR008 Bilirubin Metabolic Disorder 57 2.369
302
P CHN012 Chondrosarcoma 57 2.366
303
P PHC003 Pheochromocytoma 69 2.363
304
ADR040 Adrenal Gland Pheochromocytoma 46 2.363
305
PRP016 Paraplegia 52 2.363
306
CMM005 Common Cold 56 2.348
307
CHR178 Chromosomal Triplication 34 2.337
308
CNS004 Constipation 56 2.326
309
P ART021 Arteriosclerosis 54 2.318
310
PLY100 Polyploidy 36 2.315
311
P PRP029 Porphyria 60 2.314
312
CRB037 Cerebral Palsy 67 2.304
313
SPL018 Splenomegaly 49 2.285
314
ULC004 Ulcerative Colitis 74 2.276
315
P PSR002 Psoriasis 63 2.273
316
TTH006 Tooth Disease 51 2.271
317
P LKM002 Leukemia 67 2.261
318
P THR014 Thrombocytopenia 66 2.250
319
ORL011 Oral Cancer 60 2.250
320
P CHR345 Chronic Pain 50 2.250
321
c MCR130 Microvascular Complications of Diabetes 6 41 2.245
322
c MCR120 Microvascular Complications of Diabetes 7 47 2.245
323
c MCR113 Microvascular Complications of Diabetes 3 52 2.245
324
c MCR133 Microvascular Complications of Diabetes 4 41 2.245
325
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 2.234
326
c ALP105 Alport Syndrome 2, Autosomal Recessive 43 2.233
327
MNN009 Meningoencephalitis 48 2.218
328
c AMY091 Amyotrophic Lateral Sclerosis 1 88 2.214
329
P LTR001 Lateral Sclerosis 58 2.214
330
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 2.213
331
SDD001 Sudden Infant Death Syndrome 60 2.205
332
DSS032 Disease by Infectious Agent 55 2.198
333
P BRS044 Breast Adenocarcinoma 58 2.196
334
P LKM062 Leukemia, Acute Lymphoblastic 69 2.196
335
P MYC007 Myocardial Infarction 70 2.194
336
PST011 Pustulosis of Palm and Sole 52 2.171
337
DSS009 Disseminated Intravascular Coagulation 57 2.165
338
STT001 Status Epilepticus 59 2.162
339
P KDN017 Kidney Cancer 61 2.151
340
PRX001 Peroxisomal Disease 46 2.148
341
P ADL010 Adult Respiratory Distress Syndrome 71 2.143
342
SCK003 Sickle Cell Anemia 74 2.137
343
CNG034 Congestive Heart Failure 69 2.136
344
BBS001 Babesiosis 49 2.129
345
P NSP012 Nasopharyngeal Carcinoma 61 2.127
346
XNT003 Xanthomatosis 49 2.115
347
EMB004 Embryonal Carcinoma 56 2.113
348
P TXP001 Toxoplasmosis 60 2.113
349
P END044 Endometriosis 62 2.094
350
P TRC031 Trichorhinophalangeal Syndrome 38 2.093
351
BRN028 Brain Cancer 74 2.074
352
ENT011 Enterocolitis 55 2.064
353
c DWL002 Dowling-Degos Disease 1 58 2.062
354
P EXN002 Exanthem 58 2.061
355
NRG002 Neurogenic Bladder 55 2.057
356
CLN015 Colon Adenocarcinoma 65 2.053
357
P EPL164 Epilepsy 68 2.045
358
OTT002 Otitis Media 71 2.044
359
SVR004 Severe Combined Immunodeficiency 72 2.041
360
YLL002 Yellow Fever 61 2.006
361
P RTN016 Retinal Degeneration 52 2.006
362
LNG099 Lung Disease 62 2.005
363
ONC002 Onchocerciasis 51 2.004
364
P PLM037 Pulmonary Hypertension 72 1.982
365
P TRM003 Tremor 48 1.978
366
P INF038 Influenza 68 1.974
367
ERY004 Erysipelas 47 1.972
368
FNG016 Fungal Keratitis 39 1.968
369
PRD004 Prediabetes Syndrome 52 1.955
370
CRV035 Cervical Cancer 73 1.945
371
PRC002 Paracoccidioidomycosis 54 1.945
372
P SKN015 Skin Carcinoma 71 1.940
373
c HRD002 Hereditary Angioedema 62 1.934
374
P ANG015 Angioedema 56 1.934
375
DPH001 Diphtheria 59 1.934
376
P LNG028 Long Qt Syndrome 64 1.887
377
ALL014 Allergic Encephalomyelitis 34 1.887
378
LPD009 Lipid Storage Disease 45 1.881
379
PRM329 Premature Aging 36 1.867
380
P PLM036 Pulmonary Fibrosis 66 1.863
381
FRC011 Fructose Intolerance, Hereditary 55 1.851
382
c HNT004 Huntington Disease-Like 2 52 1.851
383
CRB090 Cerebral Hypoxia 42 1.851
384
ANL018 Analbuminemia 53 1.851
385
PHS027 Phosphoglycoprotein 1 15 1.849
386
P MCR010 Microcephaly 60 1.831
387
P ALP008 Alopecia 54 1.823
388
c GLC092 Glaucoma, Primary Open Angle 62 1.820
389
P OPN001 Open-Angle Glaucoma 55 1.820
390
P SCK005 Sickle Cell Disease 56 1.820
391
c ATS007 Autism Spectrum Disorder 72 1.808
392
c AMY088 Amyotrophic Lateral Sclerosis 3 31 1.792
393
P CRB045 Cerebellar Hypoplasia 40 1.792
394
CRD137 Cardiogenic Shock 56 1.792
395
c ACT073 Acute Leukemia 58 1.792
396
P BND020 Bone Disease 59 1.792
397
BRN018 Borna Disease 36 1.787
398
DYS015 Dysentery 50 1.781
399
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 64 1.777
400
P OVR082 Overgrowth Syndrome 49 1.776
401
RBS001 Rabies 58 1.761
402
CRD132 Cardiac Conduction Defect 60 1.759
403
END057 Endometrial Cancer 72 1.759
404
P ECL001 Eclampsia 52 1.758
405
P HRT032 Heart Disease 81 1.756
406
c SPN294 Spinocerebellar Ataxia 1 53 1.755
407
FLR002 Filariasis 55 1.755
408
ABT001 Abetalipoproteinemia 68 1.752
409
JPN002 Japanese Encephalitis 61 1.752
410
P URN019 Urinary Tract Infection 49 1.749
411
MDD011 Mood Disorder 62 1.747
412
c SYS001 Systemic Lupus Erythematosus 87 1.744
413
P LPS004 Lupus Erythematosus 61 1.744
414
DNT012 Dental Caries 53 1.744
415
PRS045 Prostatic Hypertrophy 53 1.739
416
SVR001 Severe Acute Respiratory Syndrome 67 1.733
417
c HNT011 Huntington Disease-Like 3 34 1.730
418
THR024 Thrombosis 56 1.730
419
P MJR001 Major Depressive Disorder 68 1.723
420
DPR016 Depression 65 1.723
421
c OPT053 Optic Atrophy 1 62 1.717
422
c PRG042 Progressive Familial Heart Block, Type Ia 66 1.708
423
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 49 1.708
424
c PRG043 Progressive Familial Heart Block, Type Ib 54 1.708
425
RGH001 Right Bundle Branch Block 47 1.708
426
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 1.698
427
FSC004 Fasciitis 49 1.698
428
CLF004 Cleft Lip/palate 57 1.695
429
c ACT075 Acute Myocardial Infarction 56 1.695
430
CLF001 Cleft Lip 53 1.695
431
P BCL017 B-Cell Lymphoma 59 1.674
432
SFT003 Soft Tissue Sarcoma 57 1.672
433
c PRD040 Periodontitis, Chronic 52 1.667
434
EXP004 Exophthalmos 51 1.667
435
GT001 Gout 64 1.667
436
CHL122 Cholesteatoma of Middle Ear 51 1.663
437
ACT119 Acute Promyelocytic Leukemia 62 1.663
438
HRN029 Hearing Loss, Noise-Induced 37 1.661
439
FSC002 Fascioliasis 44 1.661
440
DBT010 Diabetic Neuropathy 54 1.657
441
PRN029 Parainfluenza Virus Type 3 32 1.635
442
MTB016 Metabolic Myopathy 30 1.633
443
DWR001 Dwarfism 44 1.633
444
FDL002 Food Allergy 47 1.632
445
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 1.625
446
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 1.616
447
c LKM005 Leukemia, T-Cell, Chronic 34 1.616
448
PRN019 Perinatal Necrotizing Enterocolitis 60 1.616
449
INV001 Invasive Aspergillosis 49 1.606
450
P KRT007 Keratoconus 50 1.605
452
MNT002 Mental Depression 57 1.603
453
EXT007 Extracutaneous Mastocytoma 38 1.591
454
MST004 Mast Cell Neoplasm 42 1.591
455
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 1.591
456
P GRF003 Graft-Versus-Host Disease 71 1.591
457
c PRG020 Paragangliomas 3 39 1.590
458
PST028 Post-Traumatic Stress Disorder 59 1.588
459
P FTL001 Fetal Alcohol Syndrome 55 1.573
460
FRC013 Fructose Utilization 15 1.557
461
HMC014 Homocysteinemia 52 1.557
462
PRS021 Prostatic Adenoma 43 1.557
463
PRT013 Portal Hypertension 59 1.557
464
XRD010 Xeroderma Pigmentosum, Variant Type 73 1.555
465
ACR007 Acromegaly 70 1.554
466
PPL022 Papilloma 53 1.554
467
P HYP069 Hyperparathyroidism 62 1.554
468
SQM002 Squamous Cell Papilloma 46 1.554
469
P NPH012 Nephrotic Syndrome 60 1.554
470
PHR003 Pharyngitis 58 1.553
471
c LKM061 Leukemia, Acute Myeloid 83 1.548
472
CHR074 Choriocarcinoma 46 1.532
473
LST001 Listeriosis 59 1.532
474
P INS002 in Situ Carcinoma 53 1.532
475
KRT006 Keratoconjunctivitis 53 1.527
476
c PLM164 Pulmonary Hypertension, Primary, 1 76 1.524
477
EPD015 Epidemic Typhus 44 1.524
478
ESP021 Esophageal Cancer 83 1.516
479
P AMY004 Amyloidosis 70 1.516
480
CHC001 Chickenpox 57 1.516
481
c DVL110 Developmental and Epileptic Encephalopathy 88 20 1.516
482
PLS007 Plasmodium Falciparum Malaria 52 1.516
484
P RTN018 Retinal Disease 53 1.512
485
PRS131 Prostate Cancer/brain Cancer Susceptibility 23 1.510
486
SML019 Smallpox 55 1.510
487
IMP005 Impotence 52 1.510
488
NWC001 Newcastle Disease 47 1.510
489
CYN003 Cyanide Poisoning 22 1.497
490
ACN002 Acanthosis Nigricans 56 1.487
491
SCR011 Scrapie 39 1.487
492
P HYP061 Hypertrophic Cardiomyopathy 69 1.487
493
P LPS002 Liposarcoma 64 1.487
494
P PLY019 Polyneuropathy 52 1.487
495
MSL001 Measles 61 1.487
496
FLR001 Filarial Elephantiasis 59 1.460
497
PRS129 Prostatic Hyperplasia, Benign 49 1.454
498
P PRD006 Prader-Willi Syndrome 61 1.454
499
P MLG056 Malignant Hyperthermia 66 1.454
500
P MYT002 Myotonic Dystrophy 51 1.454
501
c FNC027 Fanconi Anemia, Complementation Group a 81 1.444
502
BRC012 Brucellosis 66 1.435
503
HYD002 Hydronephrosis 58 1.435
504
P TMP001 Temporal Lobe Epilepsy 49 1.435
505
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.434
506
c SCN007 Secondary Hyperparathyroidism 51 1.434
507
HYP014 Hyperuricemia 51 1.434
508
MSC007 Muscle Hypertrophy 64 1.433
509
CLF027 Cleft Palate, Isolated 64 1.419
510
VRL003 Variola Major 43 1.419
511
GNG013 Gingivitis 59 1.419
512
PHS025 Phosphatase, Acid, of Tissues 28 1.415
513
P MCH002 Machado-Joseph Disease 62 1.412
514
ONC007 Oncocytoma 50 1.412
516
P RNL017 Renal Oncocytoma 54 1.412
517
ALC010 Alcoholic Cardiomyopathy 42 1.412
518
RHM001 Rheumatic Fever 59 1.412
519
P OST002 Osteoporosis 76 1.399
520
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.399
521
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.399
522
PLM134 Pulmonary Fibrosis, Idiopathic 76 1.397
523
CRH001 Crohn's Disease 80 1.383
524
TRT001 Teratocarcinoma 42 1.367
525
CHL045 Choline Deficiency Disease 39 1.367
526
P PTT006 Pituitary Adenoma 55 1.344
527
P FCL005 Focal Segmental Glomerulosclerosis 57 1.344
528
MTH009 Mouth Disease 57 1.340
529
P URT039 Urticaria 58 1.340
530
P LKM071 Leukemia, Chronic Lymphocytic 75 1.338
531
TRS021 Triosephosphate Isomerase Deficiency 45 1.338
532
EPT021 Epithelial Recurrent Erosion Dystrophy 46 1.332
533
VGN023 Vaginitis 56 1.332
534
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 1.326
535
MYL009 Myelodysplastic Syndrome 67 1.326
536
HYP017 Hypophosphatemia 49 1.325
537
c ALP101 Alpha-Thalassemia 62 1.311
538
CNJ007 Conjunctivochalasis 37 1.311
539
P MNC007 Monocytic Leukemia 47 1.311
540
P MMP001 Mumps 57 1.311
541
THR004 Thrombocytosis 53 1.311
542
P CRN037 Craniosynostosis 68 1.311
543
MJD001 Majeed Syndrome 40 1.295
544
P CNJ013 Conjunctivitis 66 1.295
545
MLT157 Multiple System Atrophy 1 69 1.278
546
P MYP006 Myopia 56 1.278
547
SKN022 Skin Squamous Cell Carcinoma 54 1.278
548
PLR008 Pleurisy 50 1.278
549
GST050 Gastrointestinal System Disease 55 1.278
550
P LYM118 Lymphoma 67 1.264
551
CNN005 Connective Tissue Disease 67 1.256
552
P ATS364 Autism 69 1.248
553
CCN002 Cocaine Abuse 49 1.248
554
LYM133 Lymphoma, Hodgkin, Classic 74 1.243
555
CRN287 Carnitine Deficiency, Myopathic 17 1.243
556
P RRH023 Rare Hereditary Hemochromatosis 54 1.243
557
P OPT006 Optic Nerve Disease 58 1.243
558
NRM005 Neuromuscular Disease 63 1.243
559
HMS001 Hemosiderosis 48 1.243
560
LYM143 Lymphoma, Non-Hodgkin, Familial 75 1.236
561
P AXN001 Axonal Neuropathy 35 1.236
562
MTC005 Mitochondrial Metabolism Disease 45 1.214
563
P SCH015 Schizophrenia 74 1.214
564
CLR109 Colorectal Adenocarcinoma 50 1.214
565
P HYP098 Hypereosinophilic Syndrome 66 1.214
566
P GST044 Gastritis 55 1.214
567
ALC006 Alcoholic Hepatitis 61 1.214
568
c BSL007 Basal Cell Carcinoma 68 1.214
569
URN010 Urinary Tract Obstruction 55 1.214
570
P MYC008 Myocarditis 59 1.214
571
c GLL024 Gallbladder Disease 1 52 1.211
572
MLD001 Melioidosis 67 1.211
573
P HML001 Hemolytic-Uremic Syndrome 52 1.211
574
NRM001 Neuromyelitis Optica 61 1.211
575
PLC005 Placental Insufficiency 56 1.211
576
P ATX030 Ataxia-Telangiectasia 80 1.184
578
CTN007 Cutaneous Leishmaniasis 62 1.184
579
TLN003 Telangiectasis 51 1.184
580
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.184
581
ACT228 Acute Radiation Syndrome 30 1.170
582
BTT016 Batten-Turner Congenital Myopathy 53 1.170
583
VRL011 Viral Infectious Disease 61 1.148
584
GRW007 Growth Hormone Deficiency 46 1.139
585
P FRG001 Fragile X Syndrome 70 1.139
586
PRP027 Peripheral Vascular Disease 71 1.139
587
PLS011 Plasmacytoma 56 1.139
588
DMY004 Demyelinating Disease 50 1.139
589
P SMP003 Simpson-Golabi-Behmel Syndrome 49 1.135
590
RCK004 Rickets 68 1.135
591
MCR013 Microphthalmia 60 1.135
592
HPT022 Hepatoblastoma 54 1.123
593
P CRN024 Corneal Disease 44 1.123
594
TRN018 Transitional Cell Carcinoma 56 1.123
595
ANP005 Anaplastic Astrocytoma 57 1.123
596
ENP001 Enophthalmos 39 1.123
597
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 1.107
598
GLC024 Glucose Transporter Type 1 Deficiency Syndrome 39 1.107
599
CRD223 Cardiac Arrhythmia 63 1.095
600
c LPD033 Lipodystrophy, Congenital Generalized, Type 2 51 1.095
601
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 1.095
602
WRN001 Werner Syndrome 69 1.095
603
P MTR014 Motor Neuron Disease 65 1.095
604
c HMC039 Hemochromatosis, Type 1 73 1.058
605
LPM012 Lipomatosis, Multiple 60 1.058
606
P MLN069 Melanoma, Uveal 61 1.058
607
LMB062 Limb Ischemia 55 1.058
608
OST017 Osteomyelitis 63 1.058
609
CWP001 Cowpox 45 1.058
610
P SYS005 Systemic Scleroderma 74 1.058
611
PLM005 Pleomorphic Lipoma 40 1.058
612
MCR011 Microinvasive Gastric Cancer 41 1.058
613
P HRD217 Hereditary Optic Neuropathy 36 1.015
614
P ALP061 Alopecia, Androgenetic, 1 49 1.015
615
c THY062 Thyroid Dyshormonogenesis 5 22 1.015
616
TND005 Tendinitis 54 1.015
617
AND014 Androgenic Alopecia 47 1.015
618
FLT009 Folate Malabsorption, Hereditary 49 1.015
619
P GLC113 Galactosemia I 66 1.015
620
c PNC106 Pancreatic Agenesis 1 51 1.015
621
P HYP733 Hypercalciuria, Absorptive, 2 45 1.015
622
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 51 1.015
623
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 53 1.015
624
CNG393 Congenital Muscular Dystrophy with Hyperlaxity 12 1.015
625
P MTC133 Mitochondrial Myopathy 50 1.015
626
P RNV001 Renovascular Hypertension 49 1.015
627
AML001 Amelanotic Melanoma 37 1.015
628
CHL147 Chlamydia Pneumonia 47 1.015
629
PLC002 Plica Syndrome 35 1.015
630
P PNM007 Pneumonia 67 1.015
631
PLC008 Placenta Disease 49 1.015
632
SYN007 Synovitis 55 1.015
633
VLV011 Vulvovaginal Candidiasis 49 1.015
634
PNC034 Pancreas Disease 50 1.015
635
P WSK001 Wiskott-Aldrich Syndrome 72 0.994
636
P FML012 Familial Partial Lipodystrophy 54 0.994
637
LRN003 Learning Disability 49 0.994
638
SNS003 Sensory Peripheral Neuropathy 52 0.994
639
P FNC004 Fanconi Syndrome 60 0.994
640
P PRN023 Prion Disease 60 0.994
641
THY030 Thyroid Gland Disease 50 0.994
642
c SCL052 Scleroderma, Familial Progressive 61 0.967
643
URL001 Urolithiasis 46 0.967
644
STL007 Steel Syndrome 42 0.967
645
CHP002 Chops Syndrome 47 0.967
646
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.967
647
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.967
648
P OTS001 Otosclerosis 49 0.967
649
P BNG032 Benign Mesothelioma 53 0.967
650
PTT037 Pituitary Tumors 44 0.967
651
PSR001 Psoriatic Arthritis 62 0.922
652
DHY016 Dehydrated Hereditary Stomatocytosis 1 with or Without Pseudohyperkalemia and/or Perinatal Edema 47 0.879
653
FBR012 Fabry Disease 70 0.874
654
EST011 Esterase C 14 0.874
655
TND004 Tendinopathy 45 0.874
656
HYP025 Hyperphosphatemia 48 0.874
657
CLR108 Colorectal Adenoma 64 0.874
658
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.874
659
c LPD035 Lipodystrophy, Congenital Generalized, Type 4 45 0.874
660
ASB001 Asbestosis 47 0.874
661
ASB003 Asbestos Intoxication 32 0.874
662
CRV038 Cervical Squamous Cell Carcinoma 58 0.874
663
OVR059 Ovary Adenocarcinoma 49 0.874
664
P DRM010 Dermatomyositis 61 0.874
665
OST003 Osteonecrosis 61 0.874
666
CRN027 Corneal Neovascularization 47 0.874
667
OLG001 Oligospermia 45 0.874
668
P AGG001 Aggressive Periodontitis 55 0.874
669
SPS019 Spastic Paraparesis 38 0.859
670
STN013 Stenotrophomonas Maltophilia Infection 26 0.859
671
LCT022 Lecithin:cholesterol Acyltransferase Deficiency 58 0.859
672
P MYS003 Myasthenia Gravis 68 0.859
673
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 62 0.859
674
P MTR004 Maturity-Onset Diabetes of the Young 68 0.859
675
ANS021 Anisocoria 25 0.859
676
c MST023 Mesothelioma, Malignant 56 0.859
677
P CLC063 Celiac Disease 1 66 0.859
678
CHK001 Chikungunya 60 0.859
679
KPS004 Kaposi Sarcoma 77 0.859
680
c GLY043 Glycogen Storage Disease Xii 30 0.859
681
STF001 Stiff-Person Syndrome 58 0.859
682
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.859
683
HPT067 Hepatocellular Adenoma 43 0.859
684
P LCT002 Lactose Intolerance 52 0.859
685
P DYS154 Dystonia 64 0.859
686
VLK001 Volkmann Contracture 23 0.859
687
PLM019 Pleomorphic Liposarcoma 40 0.859
688
CRN030 Coronary Stenosis 50 0.859
689
P VSC011 Vasculitis 61 0.859
690
P OLG002 Oligodendroglioma 66 0.859
691
P CRV031 Cervical Adenocarcinoma 48 0.859
692
P THY032 Thyroiditis 57 0.859
693
NPH009 Nephrolithiasis 54 0.859
694
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.859
695
STR103 Streptococcus Pneumonia 47 0.859
696
CYS005 Cysticercosis 60 0.859
697
CRY005 Cryptococcosis 60 0.859
698
END041 Endometrial Adenocarcinoma 64 0.859
699
P BRS053 Breast Fibroadenoma 49 0.859
700
P HMR003 Hemorrhagic Disease 59 0.859
701
QFV001 Q Fever 62 0.859
702
c PRM005 Primary Hyperparathyroidism 59 0.859
703
HYP043 Hyperandrogenism 48 0.859
704
DBT002 Diabetic Autonomic Neuropathy 41 0.859
705
FML035 Familial Hyperlipidemia 55 0.859
706
P MTC069 Mitochondrial Disorders 57 0.859
707
BRN056 Bronchopulmonary Dysplasia 56 0.859
708
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 50 0.829
709
SLD003 Sialadenitis 48 0.829
710
c ATM075 Autoimmune Encephalitis 40 0.829
711
c EXD008 Exudative Vitreoretinopathy 1 71 0.766
712
CRH005 Crohn's Colitis 53 0.766
713
c PSR023 Psoriasis 1 52 0.766
714
P MJR007 Major Affective Disorder 1 42 0.766
715
P ALP009 Alopecia Areata 59 0.766
716
GLM044 Glomerular Disease 35 0.718
717
c ACQ043 Acquired Lipodystrophy 25 0.718
718
PRC051 Paracetamol Poisoning 29 0.718
719
EXR008 Exercise-Induced Malignant Hyperthermia 20 0.718
720
CHN055 Chanarin-Dorfman Syndrome 60 0.718
721
MCL009 Mcleod Syndrome 46 0.718
722
P DFN349 Deafness, Nonsyndromic Sensorineural, Mitochondrial 34 0.718
723
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.718
724
P MYS005 Myositis 56 0.718
725
CRT072 Creutzfeldt-Jakob Disease 68 0.718
726
BRG013 Buerger Disease 57 0.718
727
c LPD019 Lipodystrophy, Partial, Acquired 42 0.718
728
P FML011 Familial Adenomatous Polyposis 71 0.718
729
c SHR030 Short Qt Syndrome 44 0.718
730
P SML001 Small Cell Carcinoma 52 0.718
731
c BRG005 Brugada Syndrome 1 54 0.718
732
FNC009 Fanconi-Bickel Syndrome 53 0.718
733
LGH007 Leigh Syndrome 70 0.718
734
MYP159 Myopathy, Proximal, with Ophthalmoplegia 55 0.718
735
P SLL003 Salla Disease 45 0.718
736
ERL052 Early Repolarization Associated with Ventricular Fibrillation 22 0.718
737
c SPN283 Spinocerebellar Ataxia 37 36 0.718
739
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 0.718
740
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 65 0.718
741
c KNN009 Kenny-Caffey Syndrome, Type 1 35 0.718
742
P HMN032 Human Herpesvirus 8 48 0.718
743
INT067 Interstitial Nephritis 46 0.718
744
LMY002 Leiomyoma 51 0.718
745
P PLY041 Polymyositis 59 0.718
746
DGN001 Degenerative Disc Disease 49 0.718
747
GSG001 Gas Gangrene 52 0.718
748
P PRD021 Periodic Paralysis 41 0.718
749
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 0.718
750
ACT162 Acute Sensory Ataxic Neuropathy 24 0.718
751
ATP013 Atopic Keratoconjunctivitis 41 0.718
752
DFF036 Differentiated Thyroid Carcinoma 51 0.718
753
CLL003 Cellulitis 53 0.718
754
LNG031 Lung Benign Neoplasm 51 0.718
755
ANV001 Anovulation 47 0.718
756
HRT012 Heart Valve Disease 53 0.718
757
c LCL006 Localized Scleroderma 65 0.718
758
IMP004 Impetigo 48 0.718
759
RTN003 Retinal Ischemia 49 0.718
760
P GRV001 Graves' Disease 55 0.718
761
P SPN046 Spinal Muscular Atrophy 63 0.718
762
CRT013 Carotid Stenosis 51 0.718
763
ADT003 Auditory System Disease 49 0.718
764
RTN020 Retinal Vascular Disease 46 0.718
765
PPL002 Papillary Carcinoma 46 0.718
766
P RNL015 Renal Hypertension 45 0.718
767
P NNT058 Neonatal Diabetes 52 0.718
768
c CNG027 Congenital Hemolytic Anemia 48 0.718
769
ART008 Arteriosclerosis Obliterans 40 0.718
770
PNM001 Pneumocystosis 61 0.718
771
ALL009 Allergic Conjunctivitis 51 0.718
772
AMN003 Amnestic Disorder 54 0.718
773
DBT004 Diabetic Polyneuropathy 50 0.718
774
NRN004 Neuroendocrine Tumor 59 0.718
775
P MTR003 Mitral Valve Stenosis 53 0.718
776
P BRN022 Bronchiectasis 60 0.718
777
c JVN010 Juvenile Rheumatoid Arthritis 66 0.718
778
NNS010 Nonsyndromic Hearing Loss and Deafness, Mitochondrial 13 0.718
779
c ACT135 Acute Graft Versus Host Disease 51 0.718
780
ORP003 Oropharynx Cancer 55 0.718
781
KDN013 Kidney Hypertrophy 34 0.718
782
MYT011 Myotonia 39 0.718
783
c HRD088 Hereditary Neuropathies 33 0.718
784
BWN006 Bowen's Disease 32 0.718
785
CRL001 Cerulean Cataract 26 0.718
786
c RNG015 Ring Chromosome 2 22 0.718
787
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 44 0.718
Content
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