Search results for acetyl-coa

709 hits were found for acetyl-coa

# Family MCID Name MIFTS Score
1
ACT086 Acetyl-Coa Carboxylase Deficiency 16 60.494
2
ACT239 Acetyl-Coa Acetyltransferase-2 Deficiency 20 50.664
3
c MCP045 Mucopolysaccharidosis, Type Iiic 58 24.933
4
ALP077 Alpha-Methylacetoacetic Aciduria 52 21.743
5
MTH011 Methionine Adenosyltransferase Deficiency 17 15.288
6
MTH074 Methionine Adenosyltransferase I/iii Deficiency 42 15.140
7
HYP003 Hypermethioninemia 51 15.140
8
NNL005 Non-Alcoholic Fatty Liver Disease 63 7.631
9
FTT001 Fatty Liver Disease 61 7.489
10
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 6.300
11
NNL006 Non-Alcoholic Steatohepatitis 54 4.910
12
LPD008 Lipid Metabolism Disorder 61 3.883
13
HYP066 Hyperglycemia 60 3.105
14
P LVR013 Liver Disease 68 3.019
15
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 2.930
16
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 2.930
17
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 2.930
18
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 2.930
19
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 2.930
20
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 2.930
21
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 2.930
22
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 2.930
23
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 2.930
24
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 2.914
25
P NRB001 Neuroblastoma 66 2.805
26
P ENC018 Encephalopathy 62 2.757
27
c HYP836 Hypercholesterolemia, Familial, 1 73 2.743
28
HYP266 Hypoxia 56 2.676
29
P PRS040 Prostate Cancer 95 2.546
30
HLC001 Holocarboxylase Synthetase Deficiency 47 2.531
31
GLB002 Glioblastoma 67 2.528
32
P HPT023 Hepatocellular Carcinoma 95 2.409
33
c DNT047 Dentinogenesis Imperfecta Type 2 35 2.331
34
P BRB001 Beriberi 44 2.317
35
c MCR133 Microvascular Complications of Diabetes 4 41 2.288
36
c MCR113 Microvascular Complications of Diabetes 3 52 2.288
37
c MCR130 Microvascular Complications of Diabetes 6 41 2.288
38
c MCR120 Microvascular Complications of Diabetes 7 47 2.288
39
HYP060 Hyperinsulinism 53 2.243
40
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 2.226
41
P HYP750 Hypertriglyceridemia, Familial 62 2.217
42
P BRS047 Breast Cancer 97 2.158
43
PRP016 Paraplegia 52 2.158
44
P MYC084 Mycobacterium Tuberculosis 1 68 1.984
45
MTH071 Methane Production 25 1.969
46
PYR022 Pyruvate Dehydrogenase E1-Alpha Deficiency 64 1.940
47
c MCP001 Mucopolysaccharidosis Iii 69 1.933
48
MLN011 Malonyl-Coa Decarboxylase Deficiency 37 1.918
49
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 1.808
50
SQM006 Squamous Cell Carcinoma 59 1.808
51
ATH013 Atherosclerosis Susceptibility 63 1.778
52
CSY001 C Syndrome 61 1.759
53
HPP002 Huppke-Brendel Syndrome 7 1.759
54
48X005 48,xyyy 39 1.757
55
SLP001 Sleeping Sickness 56 1.740
56
GLC003 Glucose Intolerance 53 1.723
57
c HYP793 Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 46 1.675
58
P PNC035 Pancreatic Cancer 86 1.668
59
RNL114 Renal Cell Carcinoma, Nonpapillary 79 1.648
60
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.648
61
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 33 1.636
62
P MYP004 Myopathy 67 1.604
63
INS024 Insulin-Like Growth Factor I 77 1.585
64
MLT018 Multiple Carboxylase Deficiency 45 1.585
65
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 58 1.574
66
PRT037 Pertussis 49 1.563
67
P GST053 Gastric Cancer 82 1.513
68
c AMY091 Amyotrophic Lateral Sclerosis 1 88 1.513
69
P LTR001 Lateral Sclerosis 58 1.513
70
AGN016 Aging 54 1.500
71
PRT251 Proteinuria, Chronic Benign 58 1.486
72
BTN004 Biotin Deficiency 44 1.469
73
P BLD134 Bladder Cancer 79 1.457
74
GLM045 Glioma 62 1.453
75
GLL048 Glial Tumor 52 1.453
76
NCT004 N Acetyltransferase Deficiency 14 1.426
77
P ACN011 Acne 55 1.425
78
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 1.403
79
ISC004 Ischemia 61 1.403
80
47X002 47,xyy 48 1.403
81
BCT022 Bacterial Infectious Disease 56 1.390
82
P SKN015 Skin Carcinoma 71 1.390
83
PRP001 Propionic Acidemia 65 1.385
84
ADR016 Adrenal Cortical Carcinoma 61 1.333
85
HLX001 Helix Syndrome 47 1.328
86
HYP081 Hypolipoproteinemia 49 1.311
87
P INF038 Influenza 68 1.287
88
BRT005 Barth Syndrome 55 1.265
89
c LKM061 Leukemia, Acute Myeloid 83 1.265
90
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.242
91
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.242
92
P MLN008 Melanoma 75 1.242
93
P ALP008 Alopecia 53 1.242
94
OCL069 Ocular Motor Apraxia 57 1.218
95
ATS010 Autosomal Recessive Disease 42 1.218
96
MTB004 Metabolic Acidosis 48 1.218
97
c FTL070 Fetal Akinesia Deformation Sequence 2 36 1.218
98
P BCL017 B-Cell Lymphoma 57 1.218
99
ACR008 Acrocallosal Syndrome 70 1.193
100
c PCH010 Pachyonychia Congenita 3 43 1.193
101
P LNG032 Lung Cancer 98 1.193
102
c ATS007 Autism Spectrum Disorder 72 1.193
103
ORG002 Organic Acidemia 43 1.193
104
DBT084 Diabetes Mellitus, Ketosis-Prone 60 1.193
105
APL023 Aplasia Cutis Congenita, Nonsyndromic 46 1.184
106
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 1.184
107
CRP032 Corpus Callosum, Agenesis of 49 1.184
108
c HYP272 Hypercholesterolemia, Familial, 3 46 1.184
109
TRY001 Trypanosomiasis 50 1.166
110
MLR004 Malaria 78 1.166
111
LPT001 Leptospirosis 66 1.166
112
P LKM002 Leukemia 66 1.166
113
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 1.166
114
P MYL006 Myeloid Leukemia 60 1.166
115
GNT167 Genetic Obesity 32 1.166
116
P HPT021 Hepatitis 68 1.137
117
RNL077 Renal Fibrosis 46 1.137
118
PPL052 Papillomatosis, Confluent and Reticulated 34 1.137
119
c SML038 Small Cell Cancer of the Lung 69 1.137
120
P TXP001 Toxoplasmosis 60 1.137
121
P PLV020 Pelvic Organ Prolapse 58 1.105
122
MYL069 Myeloma, Multiple 77 1.105
123
HTC003 Hutchinson-Gilford Progeria Syndrome 65 1.105
124
MNN009 Meningoencephalitis 48 1.105
125
MST020 Mast Cell Activation Syndrome 27 1.105
126
ANP008 Anaplastic Oligoastrocytoma 31 1.105
127
TXC005 Toxic Shock Syndrome 62 1.075
128
P RTN008 Retinitis Pigmentosa 79 1.070
129
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 63 1.070
130
c RTN177 Retinitis Pigmentosa 73 36 1.070
131
c SPS099 Spastic Paraplegia 42, Autosomal Dominant 39 1.070
132
P LNG064 Lung Cancer Susceptibility 3 70 1.070
133
CHL014 Cholera 62 1.070
134
HGH043 High Grade Glioma 46 1.070
135
P NSP012 Nasopharyngeal Carcinoma 60 1.070
136
P MYC008 Myocarditis 59 1.070
137
PST092 Posttransplant Acute Limbic Encephalitis 29 1.070
138
P ATX030 Ataxia-Telangiectasia 80 1.030
139
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.030
140
INT323 Intraocular Pressure Quantitative Trait Locus 63 1.030
141
c HYP595 Hypertension, Essential 84 1.030
142
c MJR024 Major Affective Disorder 9 40 1.030
143
c MJR022 Major Affective Disorder 8 37 1.030
144
P ADN016 Adenocarcinoma 63 1.030
145
c HRD010 Hereditary Spastic Paraplegia 65 1.030
146
TLN003 Telangiectasis 51 1.030
147
P BPL003 Bipolar Disorder 56 1.030
148
SQM013 Squamous Cell Carcinoma, Head and Neck 75 1.030
149
SPS057 Spasticity 43 1.030
150
c BCT007 Bacterial Meningitis 55 1.030
151
THY029 Thyroid Carcinoma 54 1.030
152
P AST005 Asthma 76 0.983
153
c USH037 Usher Syndrome, Type Iia 50 0.983
154
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.983
155
P GRF003 Graft-Versus-Host Disease 71 0.983
156
P USH001 Usher Syndrome 64 0.983
157
HMN047 Human Cytomegalovirus Infection 59 0.983
158
P OPN001 Open-Angle Glaucoma 55 0.983
159
STH001 Saethre-Chotzen Syndrome 66 0.983
160
FLT006 Floating-Harbor Syndrome 52 0.983
161
c GLC092 Glaucoma, Primary Open Angle 61 0.983
162
c USH035 Usher Syndrome Type 2 52 0.983
163
P PNC044 Pancreatitis 61 0.983
164
LYM009 Lymphocytic Choriomeningitis 46 0.983
165
P SLP005 Sleep Disorder 62 0.983
166
ALL014 Allergic Encephalomyelitis 34 0.983
167
SKN019 Skin Melanoma 70 0.983
168
c ACT135 Acute Graft Versus Host Disease 51 0.983
169
HYP056 Hypoglycemia 65 0.962
170
c HPT003 Hepatitis a 63 0.927
171
DSS009 Disseminated Intravascular Coagulation 56 0.927
172
P VSC018 Visceral Steatosis 32 0.927
173
ART140 Arteries, Anomalies of 52 0.921
174
CYS001 Cystic Fibrosis 77 0.921
175
LGS001 Legius Syndrome 60 0.921
176
LPP008 Lipoprotein Quantitative Trait Locus 65 0.921
177
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.921
178
P FML011 Familial Adenomatous Polyposis 71 0.921
179
P KLZ004 Kala-Azar 1 41 0.921
180
c PRG020 Paragangliomas 3 39 0.921
181
P ATS364 Autism 72 0.921
182
BRC012 Brucellosis 66 0.921
183
LNG031 Lung Benign Neoplasm 51 0.921
184
BLD131 Bladder Urothelial Carcinoma 59 0.921
185
HYP082 Hypopharynx Cancer 47 0.921
186
P HRD200 Hereditary Breast Ovarian Cancer Syndrome 68 0.921
187
LSH001 Leishmaniasis 63 0.921
188
FND002 Fundus Dystrophy 55 0.921
189
P MTC069 Mitochondrial Disorders 57 0.921
190
DWR001 Dwarfism 45 0.921
191
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.878
192
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.826
193
c OVR114 Ovarian Cancer 1 60 0.773
194
c BRS110 Breast-Ovarian Cancer, Familial 1 58 0.773
195
HYM001 Hymenolepiasis 29 0.773
196
MLT006 Multidrug-Resistant Tuberculosis 47 0.773
197
P LCT001 Lactic Acidosis 50 0.757
198
PHN003 Phenylketonuria 76 0.696
199
HMP009 Haemophilus Influenzae 41 0.696
200
c TYP009 Type 2 Diabetes Mellitus 92 0.664
201
P ALZ034 Alzheimer Disease 87 0.612
202
P OVR042 Ovarian Cancer 88 0.594
203
c INH020 Inherited Metabolic Disorder 47 0.594
204
P HYP076 Hyperthyroidism 53 0.594
205
P CND004 Candidiasis 57 0.575
206
c ATR087 Atrial Standstill 1 74 0.535
207
ANX004 Anoxia 40 0.535
208
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.514
209
c TYP008 Type 1 Diabetes Mellitus 77 0.492
210
P EPL164 Epilepsy 70 0.492
211
RYS001 Reye Syndrome 49 0.492
212
P MTH008 Methylmalonic Acidemia 52 0.492
213
CYT002 Cytokine Deficiency 43 0.492
214
BRN071 Brain Injury 50 0.492
215
ACY011 Acyl-Coa Dehydrogenase Deficiency 31 0.492
216
HPT004 Hepatic Coma 43 0.469
217
HPT019 Hepatic Encephalopathy 59 0.469
218
P HNT016 Huntington Disease 73 0.445
219
P HYP265 Hypotonia 42 0.445
220
ISL099 Isolated Methylmalonic Acidemia 35 0.445
221
CND006 Candida Glabrata 29 0.445
222
PYR012 Pyruvate Dehydrogenase E1-Beta Deficiency 41 0.420
223
OVR063 Overnutrition 42 0.420
224
INS001 Insulinoma 59 0.420
225
PYR037 Pyruvate Carboxylase Deficiency 45 0.420
226
c CHR684 Chronic Kidney Disease 74 0.420
227
P DBT009 Diabetes Mellitus 67 0.420
228
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 0.393
229
c HPT073 Hepatitis C Virus 71 0.393
230
P CLR023 Colorectal Cancer 100 0.393
231
P TBR001 Tuberous Sclerosis 69 0.393
232
CNG034 Congestive Heart Failure 69 0.393
233
DNT012 Dental Caries 53 0.393
234
P THY023 Thymoma 64 0.393
235
c THY107 Thymoma, Familial 42 0.393
236
CLR030 Clear Cell Renal Cell Carcinoma 54 0.393
237
BTN003 Biotinidase Deficiency 62 0.363
239
ALC007 Alcohol Dependence 65 0.363
240
DYS015 Dysentery 50 0.363
241
P MCR010 Microcephaly 59 0.363
242
P VSC007 Vascular Disease 62 0.363
243
ALC006 Alcoholic Hepatitis 61 0.363
244
P PLY011 Polycystic Ovary Syndrome 57 0.363
245
P KDN018 Kidney Disease 72 0.363
246
TRM010 Traumatic Brain Injury 50 0.363
247
P ZLL001 Zellweger Syndrome 65 0.363
248
P MPL001 Maple Syrup Urine Disease 69 0.332
249
CNV004 Canavan Disease 61 0.332
250
INV001 Invasive Aspergillosis 48 0.332
251
P FNC004 Fanconi Syndrome 60 0.332
252
CLB022 Coloboma, Ocular, Autosomal Recessive 29 0.332
253
3HY007 3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency 50 0.332
254
END057 Endometrial Cancer 71 0.332
255
P ASP006 Aspergillosis 71 0.332
256
P ALB003 Albinism-Deafness Syndrome 33 0.332
257
c TBR025 Tuberous Sclerosis 1 84 0.332
258
MST005 Mastitis 52 0.332
259
P KDN017 Kidney Cancer 60 0.332
260
P HYP086 Hypothyroidism 69 0.332
261
SKN016 Skin Disease 62 0.332
262
SPP011 Suppression of Tumorigenicity 12 61 0.332
263
ADR007 Adrenoleukodystrophy 74 0.332
264
ADR022 Adrenomyeloneuropathy 39 0.332
265
HPT022 Hepatoblastoma 54 0.332
266
PPT005 Peptic Ulcer Disease 58 0.332
267
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.332
268
DBT010 Diabetic Neuropathy 54 0.332
269
c LKM005 Leukemia, T-Cell, Chronic 33 0.332
270
c HMN021 Human T-Cell Leukemia Virus Type 1 46 0.332
271
PRX001 Peroxisomal Disease 46 0.332
272
CRN039 Carnitine Acetyltransferase Deficiency 13 0.297
273
MSC007 Muscle Hypertrophy 64 0.297
274
P PLY014 Polycystic Kidney Disease 71 0.297
275
P MLT020 Multiple Sclerosis 79 0.297
276
VTM002 Vitamin B12 Deficiency 48 0.297
277
c 3MT007 3-Methylglutaconic Aciduria 36 0.297
278
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.297
279
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 52 0.297
280
P MYC007 Myocardial Infarction 69 0.297
281
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.297
282
CHL068 Cholestasis 61 0.297
283
LVR012 Liver Cirrhosis 62 0.297
284
c HPT001 Hepatitis C 61 0.297
285
P HYP061 Hypertrophic Cardiomyopathy 69 0.297
286
P NPH012 Nephrotic Syndrome 62 0.297
287
LYM017 Lyme Disease 63 0.297
288
P BRS044 Breast Adenocarcinoma 58 0.297
289
CLN015 Colon Adenocarcinoma 64 0.297
290
HDN002 Head Injury 44 0.297
291
c ACT134 Acute Liver Failure 57 0.297
292
BNG077 Benign Idiopathic Neonatal Seizures 22 0.297
293
P RTN024 Retinoblastoma 72 0.257
294
P SCH015 Schizophrenia 74 0.257
295
LGH007 Leigh Syndrome 70 0.257
296
WRN002 Wernicke-Korsakoff Syndrome 49 0.257
297
DWN001 Down Syndrome 70 0.257
298
c MCR115 Microvascular Complications of Diabetes 5 65 0.257
299
SZR028 Seizures, Scoliosis, and Macrocephaly/microcephaly Syndrome 36 0.257
300
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.257
301
P CHR071 Charcot-Marie-Tooth Disease 64 0.257
302
P LKD001 Leukodystrophy 58 0.257
303
c PRC016 Pre-Eclampsia 64 0.257
304
P OST002 Osteoporosis 77 0.257
305
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 63 0.257
306
NCT003 N-Acetylglutamate Synthase Deficiency 43 0.257
307
HYP690 Hyper-Beta-Alaninemia 24 0.257
308
ISV001 Isovaleric Acidemia 54 0.257
309
P SLP006 Sleep Apnea 69 0.257
310
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.257
311
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.257
312
P HRM021 Hair Morphology 2 20 0.257
313
ATM095 Autoimmune Disease 61 0.257
314
c PLM164 Pulmonary Hypertension, Primary, 1 80 0.257
315
c OPT053 Optic Atrophy 1 62 0.257
316
CNG382 Congenital Cataracts, Hearing Loss, and Neurodegeneration 28 0.257
317
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.257
318
c CHR505 Charcot-Marie-Tooth Disease, X-Linked Dominant, 6 37 0.257
319
SMT004 Smith-Lemli-Opitz Syndrome 69 0.257
320
P GLM040 Glioma Susceptibility 1 70 0.257
321
P ALC033 Alcohol Use Disorder 67 0.257
322
P NRD007 Neurodegeneration with Brain Iron Accumulation 51 0.257
323
CLT003 Colitis 63 0.257
324
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.257
325
MLG169 Malignant Astrocytoma 57 0.257
326
P INF032 Infertility 60 0.257
327
P INT068 Intestinal Disease 53 0.257
328
P PRP019 Peripheral Nervous System Disease 57 0.257
329
URM002 Uremia 47 0.257
330
IRN002 Iron Metabolism Disease 56 0.257
331
RTN020 Retinal Vascular Disease 45 0.257
332
P CYS018 Cystitis 59 0.257
333
GLN002 Glanders 38 0.257
334
TTH006 Tooth Disease 51 0.257
335
CRY005 Cryptococcosis 61 0.257
336
P GRV001 Graves' Disease 54 0.257
337
HYP006 Hypertensive Heart Disease 48 0.257
338
GST033 Gestational Diabetes 61 0.257
339
P TCD001 Tic Disorder 50 0.257
340
c ACT071 Acute Kidney Failure 60 0.257
341
P GLY013 Glycogen Storage Disease 59 0.257
342
VCC001 Vaccinia 49 0.257
343
P ART021 Arteriosclerosis 53 0.257
344
MDD011 Mood Disorder 62 0.257
345
LYS002 Lysosomal Storage Disease 51 0.257
346
STR067 Stroke, Ischemic 79 0.257
347
c OPT051 Opitz Gbbb Syndrome, Type I 45 0.257
348
P GST044 Gastritis 55 0.257
349
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.257
350
CRC021 Carcinosarcoma 62 0.257
351
MCP033 Mucopolysaccharidoses 44 0.257
352
END086 End Stage Renal Disease 54 0.257
353
P PRD008 Periodontitis 64 0.257
354
P MSC005 Muscular Dystrophy 66 0.257
355
P NRP001 Neuropathy 59 0.257
356
HLC007 Helicobacter Pylori Infection 67 0.210
357
CRN296 Carnitine Palmitoyltransferase Ii Deficiency, Infantile 64 0.210
358
c GRV008 Graves Disease 1 54 0.210
359
RFS006 Refsum Disease, Classic 63 0.210
360
c MYS055 Myasthenic Syndrome, Congenital, 6, Presynaptic 47 0.210
361
WLF001 Wolff-Parkinson-White Syndrome 63 0.210
362
HMC014 Homocysteinemia 52 0.210
363
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.210
364
WST005 West Nile Virus 55 0.210
365
RNL065 Renal Cell Carcinoma, Papillary, 1 79 0.210
366
c HNT004 Huntington Disease-Like 2 51 0.210
367
P PLM037 Pulmonary Hypertension 69 0.210
368
P FTL001 Fetal Alcohol Syndrome 55 0.210
369
c 2HY001 2-Hydroxyglutaric Aciduria 38 0.210
370
DSS032 Disease by Infectious Agent 55 0.210
371
CRB004 Cerebral Artery Occlusion 46 0.210
372
MDD018 Middle East Respiratory Syndrome 44 0.210
373
APN008 Apnea, Obstructive Sleep 66 0.210
374
DRR014 Darier-White Disease 58 0.210
375
c L2H001 L-2-Hydroxyglutaric Aciduria 49 0.210
376
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.210
377
HMR023 Hemorrhagic Cystitis 43 0.210
378
P LYM118 Lymphoma 69 0.210
379
LMB062 Limb Ischemia 55 0.210
380
ORL015 Oral Squamous Cell Carcinoma 43 0.210
381
P EXN002 Exanthem 58 0.210
383
3MT001 3-Methylcrotonyl-Coa Carboxylase Deficiency 52 0.210
384
P CRD119 Cardiac Arrest 68 0.210
385
CLR109 Colorectal Adenocarcinoma 50 0.210
386
HPT085 Hepatitis, Fulminant Viral 33 0.210
387
LGN006 Legionnaire Disease 52 0.210
388
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.210
389
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 0.210
390
HRD029 Hereditary Leiomyomatosis and Renal Cell Cancer 56 0.210
391
CLF027 Cleft Palate, Isolated 64 0.210
392
c TBR026 Tuberous Sclerosis 2 71 0.210
393
c PRX045 Peroxisome Biogenesis Disorder 1b 61 0.210
394
ACY005 Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of 54 0.210
395
LPT014 Leptin Deficiency or Dysfunction 77 0.210
396
c CRN217 Craniosynostosis 3 25 0.210
397
c VRL010 Viral Hepatitis 52 0.210
398
P KRT014 Keratosis Follicularis Spinulosa Decalvans 31 0.210
399
c FML021 Familial Hypercholesterolemia 71 0.210
400
ADN018 Adenoma 58 0.210
401
P DYS154 Dystonia 64 0.210
402
VLK001 Volkmann Contracture 22 0.210
403
KRT009 Keratosis 52 0.210
404
HST011 Histoplasmosis 54 0.210
405
CRY003 Cryptosporidiosis 55 0.210
406
WRN003 Wernicke Encephalopathy 45 0.210
407
P DMN002 Dementia 65 0.210
408
BRN028 Brain Cancer 73 0.210
409
c DLT002 Dilated Cardiomyopathy 79 0.210
410
HLL004 Hellp Syndrome 53 0.210
411
CHL123 Chlamydia 58 0.210
412
P MLN007 Male Infertility 56 0.210
413
CHG001 Chagas Disease 65 0.210
414
PRM236 Primary Biliary Cholangitis 62 0.210
415
GST023 Gastric Ulcer 52 0.210
416
FML035 Familial Hyperlipidemia 55 0.210
417
PNC129 Pancreatic Adenocarcinoma 65 0.210
418
P PLM036 Pulmonary Fibrosis 65 0.210
419
NWC001 Newcastle Disease 48 0.210
420
P OLG002 Oligodendroglioma 66 0.210
421
P CNG001 Congenital Myasthenic Syndrome 68 0.210
422
BLR008 Bilirubin Metabolic Disorder 57 0.210
423
P FBR017 Fibrosarcoma 55 0.210
424
P LPS002 Liposarcoma 64 0.210
425
PLG002 Plague 58 0.210
426
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 66 0.210
427
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.210
428
OST159 Osteogenic Sarcoma 66 0.210
429
CRB090 Cerebral Hypoxia 42 0.210
430
P CHR345 Chronic Pain 50 0.210
431
GST010 Gestational Trophoblastic Neoplasm 52 0.210
432
OVR094 Ovarian Epithelial Cancer 39 0.210
433
P HRP006 Herpes Simplex 65 0.210
434
P MSC003 Muscular Atrophy 52 0.210
435
P TRM003 Tremor 50 0.210
436
MNN024 Meningitis and Encephalitis 27 0.210
437
GLC024 Glucose Transporter Type 1 Deficiency Syndrome 38 0.210
438
SYS003 Systolic Heart Failure 49 0.210
439
LMY003 Leiomyomatosis 43 0.210
440
INT020 Intravenous Leiomyomatosis 36 0.210
441
P END047 Endophthalmitis 53 0.210
442
MTC005 Mitochondrial Metabolism Disease 45 0.210
443
CHR177 Chromophobe Renal Cell Carcinoma 54 0.210
444
MYT011 Myotonia 38 0.210
445
CHR176 Chromophil Renal Cell Carcinoma 23 0.210
446
CHR178 Chromosomal Triplication 34 0.210
447
BRN056 Bronchopulmonary Dysplasia 57 0.210
448
ANT024 Anthrax Disease 58 0.210
449
P AMY004 Amyloidosis 69 0.210
450
ULC004 Ulcerative Colitis 74 0.210
452
P CHL066 Cholangitis 51 0.210
453
NSS002 Neisseria Meningitidis Infection 47 0.210
454
CNG114 Congenital Myasthenic Syndrome with Episodic Apnea 29 0.210
455
FST010 Fasting Hypoglycemia 33 0.210
456
HYP835 Hypothalamic Obesity 38 0.210
457
ORL011 Oral Cancer 60 0.210
458
RFS003 Refsum Disease, Infantile Form 27 0.210
459
CRD137 Cardiogenic Shock 56 0.210
460
PLY100 Polyploidy 36 0.210
461
GST092 Gastroesophageal Reflux 60 0.148
462
FRC013 Fructose Utilization 15 0.148
463
OCC006 Occipital Horn Syndrome 54 0.148
464
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 61 0.148
465
PRS129 Prostatic Hyperplasia, Benign 48 0.148
466
c GLL024 Gallbladder Disease 1 53 0.148
467
c CHR646 Charcot-Marie-Tooth Disease, Axonal, Type 2b 50 0.148
468
c NPH049 Nephrotic Syndrome, Type 2 52 0.148
469
c PRD040 Periodontitis, Chronic 52 0.148
470
HSD004 Hsd10 Mitochondrial Disease 44 0.148
471
ABT001 Abetalipoproteinemia 68 0.148
472
CRN295 Carnitine Palmitoyltransferase I Deficiency 55 0.148
473
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.148
474
3MT011 3-Methylcrotonyl-Coa Carboxylase 1 Deficiency 38 0.148
475
c THY071 Thyroid Dyshormonogenesis 1 31 0.148
476
c THY056 Thyroid Dyshormonogenesis 3 32 0.148
477
WLS001 Wilson Disease 70 0.148
478
CRV035 Cervical Cancer 72 0.148
479
P LKM062 Leukemia, Acute Lymphoblastic 69 0.148
480
c FTL067 Fetal Hemoglobin Quantitative Trait Locus 6 24 0.148
481
TBL029 Tubulin, Beta 28 0.148
482
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 41 0.148
483
3HY011 3-Hydroxy-3-Methylglutaryl-Coa Synthase-2 Deficiency 31 0.148
484
FST003 Fasting Insulin Level Quantitative Trait Locus 1 6 0.148
485
c JBR018 Joubert Syndrome 4 53 0.148
486
P TMR010 Tumor Predisposition Syndrome 69 0.148
487
ANG054 Angina Pectoris 65 0.148
488
EPD015 Epidemic Typhus 44 0.148
489
P ADL017 Adult T-Cell Leukemia 54 0.148
490
DFF005 Diffuse Large B-Cell Lymphoma 55 0.148
491
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 47 0.148
492
RBF001 Riboflavin Deficiency 49 0.148
493
HYP020 Hyperprolactinemia 63 0.148
494
c NRD016 Neurodegeneration with Brain Iron Accumulation 6 49 0.148
495
P INF037 Inflammatory Bowel Disease 53 0.148
496
INT067 Interstitial Nephritis 47 0.148
497
P PRK039 Parkinsonism 55 0.148
498
P CRB045 Cerebellar Hypoplasia 40 0.148
499
BNR002 Bone Resorption Disease 47 0.148
500
ADN011 Adenoid Cystic Carcinoma 68 0.148
501
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.148
502
END062 Endometrial Hyperplasia 48 0.148
503
CYS005 Cysticercosis 60 0.148
504
P RNL015 Renal Hypertension 45 0.148
505
P MDL005 Medulloblastoma 75 0.148
506
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.148
507
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 58 0.148
508
BRK010 Burkitt Lymphoma 66 0.148
509
c FBR084 Fibromatosis, Gingival, 1 49 0.148
510
P CHN044 Chondrodysplasia Punctata Syndrome 43 0.148
511
CTR172 Citrullinemia, Classic 64 0.148
512
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 64 0.148
513
P RHM011 Rheumatoid Arthritis 81 0.148
514
ENT011 Enterocolitis 55 0.148
515
c KNN009 Kenny-Caffey Syndrome, Type 1 34 0.148
516
WTH001 Withdrawal Disorder 47 0.148
517
P SCL018 Scoliosis 57 0.148
518
P ATR011 Atrial Fibrillation 66 0.148
519
P GNG025 Gingival Fibromatosis 46 0.148
520
P LFT003 Left Ventricular Noncompaction 57 0.148
521
PRP080 Peripheral Artery Disease 54 0.148
522
STR103 Streptococcus Pneumonia 47 0.148
523
BCT021 Bacterial Sepsis 43 0.148
524
ERY003 Erythema Multiforme 56 0.148
525
CLR108 Colorectal Adenoma 63 0.148
526
NRD114 Neurodevelopmental Disorder with Dysmorphic Facies, Sleep Disturbance, and Brain Abnormalities 14 0.148
527
ANG020 Angiosarcoma 63 0.148
528
SVR097 Severe Cutaneous Adverse Reaction 68 0.148
529
DSM002 Desmosterolosis 39 0.148
530
LYM007 Lymphangioleiomyomatosis 68 0.148
531
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.148
532
c HYP837 Hypercholesterolemia, Familial, 2 47 0.148
533
P HYP838 Hyperlipidemia, Familial Combined, 3 61 0.148
534
c MST023 Mesothelioma, Malignant 56 0.148
535
c SYS001 Systemic Lupus Erythematosus 86 0.148
536
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.148
537
c RTN032 Retinal Cone Dystrophy 1 24 0.148
538
c SPS147 Spastic Paraplegia 4, Autosomal Dominant 55 0.148
539
NRL016 Neural Tube Defects 81 0.148
540
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.148
541
c BTT014 Beta-Thalassemia 72 0.148
542
c PRK071 Parkinson Disease 14, Autosomal Recessive 42 0.148
543
MSC164 Muscular Dystrophy, Congenital, Due to Integrin Alpha-7 Deficiency 47 0.148
544
NCT013 N-Acetylaspartate Deficiency 22 0.148
545
c AGM013 Agammaglobulinemia 1, Autosomal Recessive 38 0.148
546
3MT008 3-Methylcrotonyl-Coa Carboxylase 2 Deficiency 31 0.148
547
MNT317 Mental Retardation, Enteropathy, Deafness, Peripheral Neuropathy, Ichthyosis, and Keratoderma 45 0.148
548
c EPL136 Epilepsy, Childhood Absence 5 22 0.148
549
P HYP818 Hypobetalipoproteinemia, Familial, 1 60 0.148
550
CHL065 Cholangiocarcinoma 58 0.148
551
ANL018 Analbuminemia 52 0.148
552
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.148
553
CRD223 Cardiac Arrhythmia 63 0.148
554
MLT157 Multiple System Atrophy 1 69 0.148
555
URT049 Urate Oxidase, Pseudogene 24 0.148
556
c WLM013 Wilms Tumor 1 65 0.148
557
INT030 Intracranial Aneurysm 55 0.148
558
STT001 Status Epilepticus 58 0.148
559
THY006 Thymus Lymphoma 27 0.148
560
P BND020 Bone Disease 60 0.148
561
P ORF002 Orofacial Cleft 42 0.148
562
ACT098 Acute Erythroid Leukemia 55 0.148
563
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.148
564
PRP027 Peripheral Vascular Disease 71 0.148
565
P PLY019 Polyneuropathy 53 0.148
566
P MYP006 Myopia 55 0.148
567
PRV004 Periventricular Leukomalacia 52 0.148
568
c ACT068 Acute Cystitis 61 0.148
569
P DRR001 Diarrhea 55 0.148
570
CRB027 Cerebellar Disease 47 0.148
571
LRY018 Laryngeal Squamous Cell Carcinoma 47 0.148
572
PRS021 Prostatic Adenoma 43 0.148
573
c ACT027 Acute Pancreatitis 60 0.148
574
PLM009 Pleomorphic Adenoma Carcinoma 33 0.148
575
P CYS039 Cystic Kidney Disease 52 0.148
576
CRB039 Cerebrovascular Disease 65 0.148
577
P HML002 Hemolytic Anemia 62 0.148
578
URT010 Ureteral Obstruction 45 0.148
579
BRN024 Bronchitis 67 0.148
580
INT079 Intrahepatic Cholangiocarcinoma 51 0.148
581
P RTN018 Retinal Disease 53 0.148
582
EXT007 Extracutaneous Mastocytoma 38 0.148
583
AMN003 Amnestic Disorder 54 0.148
584
P OVR049 Ovarian Disease 50 0.148
585
SPT005 Spotted Fever 49 0.148
586
PRS045 Prostatic Hypertrophy 52 0.148
587
KRT002 Keratomalacia 54 0.148
588
ENT004 Enthesopathy 51 0.148
589
c ATM011 Autoimmune Hepatitis 62 0.148
590
HYP026 Hypoglycemic Coma 37 0.148
591
P ICH004 Ichthyosis 56 0.148
592
SYN007 Synovitis 54 0.148
593
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.148
594
PPL022 Papilloma 53 0.148
595
TRN018 Transitional Cell Carcinoma 56 0.148
596
HYP014 Hyperuricemia 51 0.148
597
HYP080 Hypogonadism 49 0.148
598
CRB037 Cerebral Palsy 67 0.148
599
RLP003 Relapsing Fever 50 0.148
600
CCC001 Coccidioidomycosis 58 0.148
601
P ECL001 Eclampsia 52 0.148
602
P HYP069 Hyperparathyroidism 62 0.148
603
SQM002 Squamous Cell Papilloma 45 0.148
604
P RNV001 Renovascular Hypertension 49 0.148
605
P DDN001 Duodenal Ulcer 53 0.148
606
DMP001 Dumping Syndrome 43 0.148
607
RFT001 Rift Valley Fever 50 0.148
608
P HYD006 Hydrocephalus 63 0.148
609
QFV001 Q Fever 61 0.148
610
P ESP024 Esophagitis 60 0.148
611
HMS001 Hemosiderosis 48 0.148
612
MRS001 Marasmus 41 0.148
613
PLC002 Plica Syndrome 35 0.148
614
PLM010 Pulmonary Edema 54 0.148
615
DPH001 Diphtheria 59 0.148
616
PRD004 Prediabetes Syndrome 52 0.148
617
DBT002 Diabetic Autonomic Neuropathy 40 0.148
618
P HRT032 Heart Disease 84 0.148
619
LST001 Listeriosis 59 0.148
620
PNM001 Pneumocystosis 60 0.148
621
PLC005 Placental Insufficiency 56 0.148
622
GNG013 Gingivitis 59 0.148
623
P RHB003 Rhabdomyosarcoma 66 0.148
624
CHR074 Choriocarcinoma 46 0.148
625
c SCN007 Secondary Hyperparathyroidism 51 0.148
626
MSN004 Mesenchymal Cell Neoplasm 42 0.148
627
MST004 Mast Cell Neoplasm 41 0.148
628
CRV038 Cervical Squamous Cell Carcinoma 56 0.148
629
ADR005 Adrenal Carcinoma 61 0.148
630
ADR004 Adrenal Cortical Adenocarcinoma 38 0.148
631
CYS011 Cystoisosporiasis 27 0.148
632
TLR001 Tularemia 56 0.148
633
P BNG032 Benign Mesothelioma 53 0.148
634
P TMP001 Temporal Lobe Epilepsy 49 0.148
635
NRL005 Neurilemmoma 60 0.148
636
GST040 Gastric Adenocarcinoma 66 0.148
637
ANP005 Anaplastic Astrocytoma 59 0.148
638
CPN001 C-P Angle Neurinoma 10 0.148
639
MNK001 Menkes Disease 64 0.148
640
KRN002 Kearns-Sayre Syndrome 63 0.148
641
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 62 0.148
642
P CTR177 Citrullinemia, Type Ii, Adult-Onset 55 0.148
643
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.148
644
46X083 46,xy Gonadal Dysgenesis with Minifascicular Neuropathy 33 0.148
645
VRL017 Viral Hemorrhagic Fever 35 0.148
646
WLL004 Wallerian Degeneration 38 0.148
647
ALD013 Aldosterone-Producing Adenoma 36 0.148
648
ANR040 Aneurysm 60 0.148
649
P CRB088 Cerebral Atrophy 33 0.148
650
CRB089 Cerebral Beriberi 19 0.148
651
HRT012 Heart Valve Disease 53 0.148
652
ANG018 Angiomyolipoma 45 0.148
653
PRC002 Paracoccidioidomycosis 53 0.148
654
SFT003 Soft Tissue Sarcoma 57 0.148
655
P THL005 Thalassemia 56 0.148
656
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 41 0.148
657
TTR011 Tetraploidy 43 0.148
658
P DYS021 Dysautonomia 38 0.148
659
DYS073 Dysphagia 53 0.148
660
XLN239 X-Linked Distal Hereditary Motor Neuropathy 12 0.148
661
CRV002 Cervix Uteri Carcinoma in Situ 48 0.148
662
MYC005 Myocardial Stunning 45 0.148
663
CHR121 Charcot-Marie-Tooth Neuropathy X Type 5 17 0.148
664
LNG099 Lung Disease 62 0.148
665
GLC008 Glucose Metabolism Disease 40 0.148
666
YLL002 Yellow Fever 61 0.148
667
CLF001 Cleft Lip 54 0.148
668
P LNG035 Lung Large Cell Carcinoma 53 0.148
669
P EYD002 Eye Disease 57 0.148
670
PLM014 Pleomorphic Adenoma 51 0.148
671
MCP006 Mucoepidermoid Carcinoma 48 0.148
672
P MNC007 Monocytic Leukemia 48 0.148
673
HYP264 Hypertonia 36 0.148
674
SPN186 Spinal Cord Injury 61 0.148
675
CRC034 Carcinoma Showing Thymus-Like Differentiation 22 0.148
676
CRV045 Cervical Intraepithelial Neoplasia 38 0.148
677
P CHR342 Chiari Malformation 41 0.148
678
MTC004 Mitochondrial Encephalomyopathy 43 0.148
679
OST012 Osteoarthritis 77 0.148
680
P ART022 Arthritis 70 0.148
681
P LPS004 Lupus Erythematosus 61 0.148
682
P AXN001 Axonal Neuropathy 33 0.148
683
PLC008 Placenta Disease 49 0.148
684
MSL001 Measles 61 0.148
685
CLP007 Clpb Deficiency 13 0.148
686
FHT001 Fh Tumor Predisposition Syndrome 26 0.148
687
c SPS091 Spastic Paraplegia 4 27 0.148
688
DST006 Diastolic Heart Failure 45 0.148
689
IRR002 Irritable Bowel Syndrome 65 0.148
690
LPD009 Lipid Storage Disease 45 0.148
691
PRN019 Perinatal Necrotizing Enterocolitis 60 0.148
692
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 44 0.148
693
MYC013 Mycobacterium Abscessus 42 0.148
694
NNT017 Neonatal Adrenoleukodystrophy 52 0.148
695
OLG006 Oligoastrocytoma 35 0.148
696
MYC019 Mycobacterium Marinum 29 0.148
697
LSS003 Lassa Fever 49 0.148
698
FBR019 Fibromatosis 44 0.148
699
P HYP055 Hypoplastic Left Heart Syndrome 65 0.148
700
AMB001 Amebiasis 56 0.148
701
CLF056 Cleft Lip with or Without Cleft Palate 43 0.148
702
ART109 Arterial Thoracic Outlet Syndrome 24 0.148
703
P RRH023 Rare Hereditary Hemochromatosis 53 0.148
704
INH023 Inherited Cancer-Predisposing Syndrome 53 0.148
705
ERY066 Erythema Multiforme Major 29 0.148
706
ARG004 Argyria 26 0.148
707
P PLY188 Polyendocrinopathy 29 0.148
708
P OVR082 Overgrowth Syndrome 42 0.148
709
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 0.148
Content
Loading form....