Search results for 4-phenylbutyric acid

288 hits were found for 4-phenylbutyric acid

# Family MCID Name MIFTS Score
1
CHL068 Cholestasis 61 0.300
2
P LVR013 Liver Disease 68 0.266
3
FTT001 Fatty Liver Disease 61 0.251
4
LVR012 Liver Cirrhosis 62 0.231
5
P KDN018 Kidney Disease 72 0.228
6
P NRB001 Neuroblastoma 72 0.221
7
CYS001 Cystic Fibrosis 81 0.219
8
P CLR023 Colorectal Cancer 99 0.216
9
HYP014 Hyperuricemia 52 0.216
10
ACT119 Acute Promyelocytic Leukemia 63 0.216
11
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.209
12
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.208
13
P SZR006 Seizure Disorder 56 0.202
14
48X005 48,xyyy 39 0.197
15
VSL002 Visual Epilepsy 59 0.196
16
LPD008 Lipid Metabolism Disorder 62 0.193
17
CLT003 Colitis 62 0.188
18
OST012 Osteoarthritis 78 0.187
19
P GLM045 Glioma 63 0.185
20
GLL048 Glial Tumor 45 0.183
21
GT001 Gout 64 0.180
22
BNR002 Bone Resorption Disease 48 0.179
23
GLB015 Glioblastoma Multiforme 75 0.176
24
ISC004 Ischemia 58 0.176
25
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.175
26
P ENC018 Encephalopathy 61 0.175
27
ATH013 Atherosclerosis Susceptibility 65 0.169
28
c HYP836 Hypercholesterolemia, Familial, 1 73 0.169
29
P HYP750 Hypertriglyceridemia, Familial 62 0.168
30
P PRS040 Prostate Cancer 97 0.166
31
HYP066 Hyperglycemia 61 0.164
32
P LKM002 Leukemia 68 0.164
33
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.159
34
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.154
35
P HNT016 Huntington Disease 72 0.154
36
P PNC035 Pancreatic Cancer 84 0.153
37
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.153
38
PLM001 Pulmonary Tuberculosis 69 0.153
39
c CHR684 Chronic Kidney Disease 70 0.152
40
DFC004 Deficiency Anemia 70 0.152
41
HPT004 Hepatic Coma 45 0.151
42
ATM095 Autoimmune Disease 62 0.151
43
P ADN016 Adenocarcinoma 64 0.149
44
P MYL006 Myeloid Leukemia 60 0.148
45
NNL006 Non-Alcoholic Steatohepatitis 54 0.148
46
P LNG032 Lung Cancer 98 0.144
47
HPT019 Hepatic Encephalopathy 60 0.143
48
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.142
49
c ACT027 Acute Pancreatitis 60 0.141
50
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.139
51
P ALZ034 Alzheimer Disease 88 0.137
52
P NRP001 Neuropathy 56 0.135
53
c LKM061 Leukemia, Acute Myeloid 84 0.135
54
HYP266 Hypoxia 57 0.133
55
IRN002 Iron Metabolism Disease 57 0.132
56
MYL069 Myeloma, Multiple 85 0.131
57
c MCR120 Microvascular Complications of Diabetes 7 47 0.130
58
c MCR113 Microvascular Complications of Diabetes 3 52 0.130
59
c MCR130 Microvascular Complications of Diabetes 6 41 0.130
60
c MCR133 Microvascular Complications of Diabetes 4 41 0.130
61
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.129
62
CHL014 Cholera 59 0.128
63
P BCL017 B-Cell Lymphoma 58 0.128
64
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.128
65
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.128
66
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.128
67
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.128
68
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.128
69
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.128
70
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.128
71
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.128
72
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.128
73
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.128
74
END086 End Stage Renal Disease 51 0.126
75
P GST053 Gastric Cancer 83 0.125
76
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.124
77
P MYP004 Myopathy 70 0.123
78
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.121
79
NPH009 Nephrolithiasis 55 0.121
80
P LTR001 Lateral Sclerosis 54 0.121
81
P FML355 Familial Intrahepatic Cholestasis 38 0.120
82
RCK004 Rickets 68 0.119
83
GLC003 Glucose Intolerance 54 0.119
84
SPN186 Spinal Cord Injury 60 0.119
85
LNG099 Lung Disease 60 0.118
86
P MPL001 Maple Syrup Urine Disease 69 0.114
87
P CTR002 Cataract 60 0.113
88
c SYS001 Systemic Lupus Erythematosus 86 0.112
89
P PRP019 Peripheral Nervous System Disease 58 0.110
90
c INH020 Inherited Metabolic Disorder 47 0.108
91
CHL079 Children's Interstitial Lung Disease 26 0.108
92
P THL005 Thalassemia 60 0.108
93
IMM167 Immune Deficiency Disease 78 0.106
94
P MSC005 Muscular Dystrophy 66 0.105
95
P MSC003 Muscular Atrophy 52 0.104
96
MYL009 Myelodysplastic Syndrome 70 0.104
97
c SML038 Small Cell Cancer of the Lung 65 0.104
98
c MLG068 Malignant Glioma 46 0.104
99
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.104
100
TXC005 Toxic Shock Syndrome 62 0.103
101
P PNC044 Pancreatitis 61 0.103
102
CLN015 Colon Adenocarcinoma 65 0.102
103
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.102
104
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.102
105
ADL002 Adult Syndrome 70 0.101
106
P GLM040 Glioma Susceptibility 1 81 0.099
107
ANX010 Anxiety 73 0.098
108
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.097
109
P LNG064 Lung Cancer Susceptibility 3 78 0.095
110
P PLM036 Pulmonary Fibrosis 65 0.095
111
c PRS136 Prostate Cancer, Hereditary, 6 33 0.094
112
c PRS130 Prostate Cancer, Hereditary, 8 32 0.094
113
P CNR004 Cone-Rod Dystrophy 2 73 0.094
114
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.093
115
P MDL005 Medulloblastoma 77 0.093
116
P SCK005 Sickle Cell Disease 50 0.092
117
P MYC084 Mycobacterium Tuberculosis 1 68 0.092
118
P DMN002 Dementia 66 0.091
119
RNL077 Renal Fibrosis 47 0.091
120
P DYS154 Dystonia 65 0.090
121
c LKM063 Leukemia, Chronic Myeloid 72 0.089
122
P LKM071 Leukemia, Chronic Lymphocytic 79 0.088
123
BLR008 Bilirubin Metabolic Disorder 57 0.087
124
RTN023 Retinitis 46 0.087
125
NRR001 Neuroretinitis 42 0.087
126
BRN028 Brain Cancer 74 0.086
127
HYP081 Hypolipoproteinemia 51 0.086
128
PRT013 Portal Hypertension 59 0.085
129
P RTN008 Retinitis Pigmentosa 79 0.085
130
PLS009 Plasma Cell Neoplasm 51 0.085
131
ACY011 Acyl-Coa Dehydrogenase Deficiency 38 0.085
132
P PRK057 Parkinson Disease, Late-Onset 78 0.085
133
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.082
134
P RCT021 Rectum Cancer 52 0.082
135
c LKM005 Leukemia, T-Cell, Chronic 34 0.082
136
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.082
137
P GRF003 Graft-Versus-Host Disease 72 0.081
138
c BTT014 Beta-Thalassemia 74 0.081
139
ERY051 Erythroleukemia, Familial 56 0.081
140
P OPN001 Open-Angle Glaucoma 49 0.081
141
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.080
142
LNG031 Lung Benign Neoplasm 51 0.080
143
P ANP001 Anaplastic Large Cell Lymphoma 58 0.080
144
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.078
145
c FML021 Familial Hypercholesterolemia 66 0.077
146
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.077
147
c CHR064 Chronic Monocytic Leukemia 33 0.076
148
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.076
149
MSC157 Muscular Dystrophy, Duchenne Type 72 0.075
150
c BRN108 Branchiootic Syndrome 1 62 0.075
151
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.074
152
HMG005 Hemoglobinopathy 56 0.074
153
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.073
154
URT010 Ureteral Obstruction 45 0.073
155
c GLC092 Glaucoma, Primary Open Angle 62 0.073
156
BRK010 Burkitt Lymphoma 67 0.073
157
CRT017 Cartilage Disease 54 0.073
158
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 59 0.072
159
URC002 Urea Cycle Disorder 51 0.071
160
SCK003 Sickle Cell Anemia 74 0.071
161
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.071
162
P NRV007 Nervous System Disease 66 0.071
163
P SPN046 Spinal Muscular Atrophy 62 0.070
164
HPT022 Hepatoblastoma 56 0.070
165
c CHL132 Cholestasis, Progressive Familial Intrahepatic, 1 57 0.069
166
P MNC007 Monocytic Leukemia 53 0.068
167
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 33 0.068
168
P FTL001 Fetal Alcohol Syndrome 57 0.068
169
BRT054 Brittle Bone Disorder 72 0.067
170
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 58 0.067
171
P MTR014 Motor Neuron Disease 65 0.067
172
P ADL017 Adult T-Cell Leukemia 56 0.066
173
c CHL134 Cholestasis, Benign Recurrent Intrahepatic, 1 56 0.066
174
HMT002 Hematologic Cancer 62 0.066
175
INT002 Intermittent Claudication 61 0.065
176
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.064
177
FCT007 Factor Vii Deficiency 67 0.064
178
PRP016 Paraplegia 52 0.064
179
MNT001 Mantle Cell Lymphoma 69 0.063
180
MYC006 Mycosis Fungoides 66 0.063
181
P FLL037 Follicular Lymphoma 67 0.062
182
SPN041 Spinal Cord Disease 56 0.062
183
LYM040 Lymphoblastic Lymphoma 54 0.061
184
FNG017 Fungal Infectious Disease 53 0.061
185
EWN003 Ewing Sarcoma 69 0.061
186
ERL001 Early Myoclonic Encephalopathy 62 0.061
187
P MYS005 Myositis 56 0.061
188
c CNT035 Central Nervous System Disease 52 0.061
189
ARG002 Argininosuccinic Aciduria 61 0.060
190
P BNG030 Benign Ependymoma 60 0.060
191
NRM005 Neuromuscular Disease 64 0.059
192
RFR010 Refractory Anemia 48 0.059
193
CLL010 Cellular Ependymoma 54 0.059
194
AMN002 Amino Acid Metabolic Disorder 39 0.059
195
VTM033 Vitamin K Deficiency Bleeding 48 0.059
196
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.058
197
AMN012 Aminoacidopathies 21 0.058
198
CTR172 Citrullinemia, Classic 64 0.057
199
P EPD016 Epidermolysis Bullosa 53 0.057
200
MYL031 Myeloproliferative Neoplasm 66 0.057
201
KHL003 Kohlschutter-Tonz Syndrome 65 0.057
202
P CHR285 Chronic Myelomonocytic Leukemia 60 0.057
203
INC002 Inclusion Body Myositis 58 0.057
204
INT066 Interstitial Lung Disease 60 0.057
205
RTN003 Retinal Ischemia 50 0.057
206
c FLL041 Follicular Lymphoma 1 49 0.057
207
CLN045 Colonic Benign Neoplasm 46 0.057
208
c FTL006 Fetal Alcohol Spectrum Disorder 43 0.057
209
WLS001 Wilson Disease 71 0.056
210
c ALP101 Alpha-Thalassemia 62 0.056
211
P DBT005 Diabetes Insipidus 55 0.055
212
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.055
213
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.054
214
PNC034 Pancreas Disease 48 0.054
215
c PNC106 Pancreatic Agenesis 1 51 0.053
216
SZR001 Sezary's Disease 60 0.053
217
c CHL116 Cholestasis, Intrahepatic, of Pregnancy, 1 53 0.053
218
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.052
219
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.052
220
PLS025 Plasmablastic Lymphoma 47 0.052
221
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.052
222
FBR012 Fabry Disease 72 0.051
223
c LKM070 Leukemia, Acute Monocytic 57 0.051
224
BNM001 Bone Marrow Cancer 43 0.051
225
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.051
226
c HYP768 Hyperlipoproteinemia, Type I 67 0.051
227
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.051
228
GRM010 Germ Cells Tumors 34 0.050
229
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.050
230
c CHR417 Chronic Graft Versus Host Disease 57 0.049
231
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.049
232
MRG003 Marginal Zone B-Cell Lymphoma 52 0.049
233
ACT200 Acute Monoblastic Leukemia 52 0.049
234
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 59 0.048
235
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.048
236
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.048
237
ATP014 Atp8b1 Deficiency 25 0.048
238
CYS014 Cystadenocarcinoma 51 0.047
239
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.047
240
P INB001 Inborn Amino Acid Metabolism Disorder 10 0.047
241
ISL001 Islet Cell Tumor 56 0.046
242
DNT001 Dental Fluorosis 43 0.046
243
SCP002 Scapuloperoneal Spinal Muscular Atrophy 56 0.046
244
ATY042 Atypical Chronic Myeloid Leukemia 49 0.046
245
INT054 Intraocular Lymphoma 48 0.046
246
APP009 Appendix Adenocarcinoma 44 0.046
247
PYR022 Pyruvate Dehydrogenase E1-Alpha Deficiency 60 0.045
248
MCN001 Mucinous Adenocarcinoma 49 0.045
249
GRM005 Germ Cell Cancer 47 0.044
251
MYC080 Myoclonic Epilepsy of Unverricht and Lundborg 52 0.044
252
INT253 Intestinal Benign Neoplasm 45 0.044
253
P OVR096 Overlap Myositis 27 0.044
254
P PNB001 Pineoblastoma 50 0.043
255
P ACH003 Achromatopsia 61 0.042
256
P EPD003 Epidermolysis Bullosa Simplex 58 0.042
257
SPL004 Splenic Marginal Zone Lymphoma 51 0.042
258
P CRN025 Corneal Dystrophy 49 0.042
259
P ART106 Arterial Calcification, Generalized, of Infancy, 1 46 0.042
260
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 45 0.042
261
MCN008 Mucinous Cystadenocarcinoma 40 0.042
262
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.042
263
ACT114 Acute Myeloblastic Leukemia Without Maturation 33 0.042
264
P AML002 Amelogenesis Imperfecta 55 0.041
265
P CLR019 Color Blindness 48 0.041
266
CLN002 Colon Mucinous Adenocarcinoma 28 0.041
267
c SPN395 Spinal Muscular Atrophy, Type Ii 55 0.040
268
c SPN393 Spinal Muscular Atrophy, Type I 52 0.040
269
c CHL118 Cholestasis, Benign Recurrent Intrahepatic, 2 44 0.040
270
c ADL093 Adult Acute Monocytic Leukemia 20 0.040
271
P PLZ001 Pelizaeus-Merzbacher Disease 64 0.039
272
P HYP097 Hyperekplexia 61 0.039
273
c ACH020 Achromatopsia 2 50 0.039
274
CHL155 Childhood Spinal Muscular Atrophy 29 0.039
275
P PSD087 Pseudoxanthoma Elasticum 65 0.038
276
c WLF013 Wolfram Syndrome 1 60 0.038
277
CRB151 Cerebral Creatine Deficiency Syndrome 1 52 0.038
278
TRT020 Tritanopia 49 0.036
279
CLR033 Color Vision Deficiency 41 0.036
280
GRN055 Granular Corneal Dystrophy 36 0.036
281
PYR012 Pyruvate Dehydrogenase E1-Beta Deficiency 35 0.036
282
SML008 Small Intestine Lymphoma 33 0.036
283
P WLF004 Wolfram Syndrome 60 0.035
284
AMY086 Amyotrophy, Hereditary Neuralgic 48 0.035
285
MYC079 Myoclonic Epilepsy of Lafora 64 0.033
286
c DYS191 Dystonia 1, Torsion, Autosomal Dominant 50 0.033
287
c ACH038 Achromatopsia 7 39 0.033
288
PRG074 Progressive Myoclonus Epilepsy, Lafora Type 29 0.033
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