Search results for acetyl-coa

196 hits were found for acetyl-coa

# Family MCID Name MIFTS Score
1
ACT086 Acetyl-Coa Carboxylase Deficiency 14 13.422
2
ACT239 Acetyl-Coa Acetyltransferase-2 Deficiency 24 12.211
3
c MCP045 Mucopolysaccharidosis, Type Iiic 40 11.000
4
ALP077 Alpha-Methylacetoacetic Aciduria 56 7.677
5
NCT004 N Acetyltransferase Deficiency 15 5.479
6
HYP003 Hypermethioninemia 44 5.428
7
MTH074 Methionine Adenosyltransferase I/iii Deficiency 42 5.428
8
MTH011 Methionine Adenosyltransferase Deficiency 18 5.428
9
FTT001 Fatty Liver Disease 61 0.231
10
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.231
11
P BRS047 Breast Cancer 96 0.175
12
LPD008 Lipid Metabolism Disorder 62 0.175
13
P ENC018 Encephalopathy 61 0.175
14
P NRB001 Neuroblastoma 71 0.163
15
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.163
16
NNL006 Non-Alcoholic Steatohepatitis 51 0.163
17
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.138
18
c MCP001 Mucopolysaccharidosis Iii 65 0.138
19
P HPT023 Hepatocellular Carcinoma 100 0.124
20
GLB015 Glioblastoma Multiforme 75 0.124
21
P MCP040 Mucopolysaccharidosis-Plus Syndrome 64 0.124
22
PRP016 Paraplegia 53 0.124
23
c MCR113 Microvascular Complications of Diabetes 3 52 0.124
24
c MCR120 Microvascular Complications of Diabetes 7 47 0.124
25
P BRB001 Beriberi 44 0.124
26
c ATS307 Autosomal Recessive Cerebellar Ataxia 41 0.124
27
c MCR130 Microvascular Complications of Diabetes 6 41 0.124
28
c MCR133 Microvascular Complications of Diabetes 4 41 0.124
29
c DNT047 Dentinogenesis Imperfecta Type 2 33 0.124
30
P PNC035 Pancreatic Cancer 84 0.107
31
P HYP750 Hypertriglyceridemia, Familial 61 0.107
32
HYP066 Hyperglycemia 61 0.107
33
CSY001 C Syndrome 50 0.107
34
48X005 48,xyyy 39 0.107
35
MTH071 Methane Production 26 0.107
36
HPP002 Huppke-Brendel Syndrome 7 0.107
37
P CLR023 Colorectal Cancer 98 0.087
38
P LNG032 Lung Cancer 97 0.087
39
P PRS040 Prostate Cancer 97 0.087
40
P OVR042 Ovarian Cancer 89 0.087
41
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.087
42
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.087
43
INS024 Insulin-Like Growth Factor I 79 0.087
44
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.087
45
P NRF023 Neurofibromatosis, Type Ii 76 0.087
46
c HYP836 Hypercholesterolemia, Familial, 1 72 0.087
47
P SKN015 Skin Carcinoma 67 0.087
48
PRT037 Pertussis 65 0.087
49
P ADN016 Adenocarcinoma 64 0.087
50
ISC004 Ischemia 60 0.087
51
SQM006 Squamous Cell Carcinoma 60 0.087
52
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 57 0.087
53
HYP060 Hyperinsulinism 54 0.087
54
P LTR001 Lateral Sclerosis 53 0.087
55
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.087
56
SLP001 Sleeping Sickness 48 0.087
57
HLC001 Holocarboxylase Synthetase Deficiency 48 0.087
58
MLT018 Multiple Carboxylase Deficiency 45 0.087
59
c HYP793 Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 44 0.087
60
PPL052 Papillomatosis, Confluent and Reticulated 34 0.087
61
c HYP595 Hypertension, Essential 84 0.062
62
c LKM061 Leukemia, Acute Myeloid 83 0.062
63
P GST053 Gastric Cancer 83 0.062
64
P ATX030 Ataxia-Telangiectasia 83 0.062
65
CYS001 Cystic Fibrosis 80 0.062
66
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.062
67
P BLD134 Bladder Cancer 78 0.062
68
P LNG064 Lung Cancer Susceptibility 3 77 0.062
69
P RTN008 Retinitis Pigmentosa 77 0.062
70
ULC004 Ulcerative Colitis 73 0.062
71
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.062
72
P FML011 Familial Adenomatous Polyposis 72 0.062
73
P GRF003 Graft-Versus-Host Disease 71 0.062
74
MLN008 Melanoma 69 0.062
75
P LVR013 Liver Disease 68 0.062
76
ACR008 Acrocallosal Syndrome 68 0.062
77
P THR014 Thrombocytopenia 68 0.062
78
SKN019 Skin Melanoma 67 0.062
79
c ATS007 Autism Spectrum Disorder 67 0.062
80
P HPT021 Hepatitis 67 0.062
81
STH001 Saethre-Chotzen Syndrome 67 0.062
82
AND002 Androgen Insensitivity Syndrome 66 0.062
83
LPT001 Leptospirosis 66 0.062
84
P ASP006 Aspergillosis 66 0.062
85
HYP056 Hypoglycemia 66 0.062
86
ATH013 Atherosclerosis Susceptibility 66 0.062
87
c HRD010 Hereditary Spastic Paraplegia 66 0.062
88
c PRD013 Periodic Fever, Familial, Autosomal Dominant 65 0.062
89
P ATS364 Autism 65 0.062
90
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.062
91
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.062
92
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.062
93
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.062
94
P MYP004 Myopathy 64 0.062
95
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 63 0.062
96
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 63 0.062
97
LSH001 Leishmaniasis 63 0.062
98
P CRN018 Coronary Artery Anomaly 63 0.062
99
P ANR048 Aniridia 1 63 0.062
100
ANR007 Anorexia Nervosa 63 0.062
101
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.062
102
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.062
103
c GLC092 Glaucoma, Primary Open Angle 62 0.062
104
PYR022 Pyruvate Dehydrogenase E1-Alpha Deficiency 62 0.062
105
TXC005 Toxic Shock Syndrome 61 0.062
106
BRC012 Brucellosis 61 0.062
107
ACN002 Acanthosis Nigricans 60 0.062
108
P TXP001 Toxoplasmosis 60 0.062
109
P MYL006 Myeloid Leukemia 60 0.062
110
P SLP005 Sleep Disorder 59 0.062
111
P MYC008 Myocarditis 59 0.062
112
DBT084 Diabetes Mellitus, Ketosis-Prone 59 0.062
113
P TRC086 Trichohepatoenteric Syndrome 1 59 0.062
114
P PLV020 Pelvic Organ Prolapse 59 0.062
115
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.062
116
P AXN002 Axenfeld-Rieger Syndrome 58 0.062
117
P BCL017 B-Cell Lymphoma 58 0.062
118
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 58 0.062
119
LGS001 Legius Syndrome 57 0.062
120
DSS009 Disseminated Intravascular Coagulation 57 0.062
121
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.062
122
CYT008 Cytomegalovirus Infection 56 0.062
123
THR024 Thrombosis 56 0.062
124
P BPL003 Bipolar Disorder 56 0.062
125
P ALP008 Alopecia 56 0.062
126
AGN016 Aging 56 0.062
127
P MTC069 Mitochondrial Disorders 56 0.062
128
c BCT007 Bacterial Meningitis 55 0.062
129
CHL014 Cholera 55 0.062
130
BRT005 Barth Syndrome 53 0.062
131
ART140 Arteries, Anomalies of 53 0.062
132
THR013 Thoracic Outlet Syndrome 53 0.062
133
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.062
134
c GLL024 Gallbladder Disease 1 52 0.062
135
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.062
136
c ACT135 Acute Graft Versus Host Disease 51 0.062
137
OCL069 Ocular Motor Apraxia 51 0.062
138
TLN003 Telangiectasis 51 0.062
139
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.062
140
LNG031 Lung Benign Neoplasm 50 0.062
141
TRY001 Trypanosomiasis 50 0.062
142
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 50 0.062
143
MTB004 Metabolic Acidosis 50 0.062
144
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.062
145
P OPN001 Open-Angle Glaucoma 49 0.062
146
MNN009 Meningoencephalitis 49 0.062
147
CRP032 Corpus Callosum, Agenesis of 49 0.062
148
c INV001 Invasive Aspergillosis 48 0.062
149
ATS010 Autosomal Recessive Disease 48 0.062
150
FLT006 Floating-Harbor Syndrome 48 0.062
151
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.062
152
ADR016 Adrenal Cortical Carcinoma 48 0.062
153
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.062
154
MLT006 Multidrug-Resistant Tuberculosis 47 0.062
155
HYP082 Hypopharynx Cancer 47 0.062
156
RNL077 Renal Fibrosis 47 0.062
157
LYM009 Lymphocytic Choriomeningitis 46 0.062
158
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.062
159
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.062
160
APL023 Aplasia Cutis Congenita, Nonsyndromic 46 0.062
161
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.062
162
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.062
163
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.062
164
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.062
165
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.062
166
DWR001 Dwarfism 44 0.062
167
c PCH010 Pachyonychia Congenita 3 43 0.062
168
c HYP272 Hypercholesterolemia, Familial, 3 43 0.062
169
ORG002 Organic Acidemia 43 0.062
170
P KLZ004 Kala-Azar 1 41 0.062
171
c MJR024 Major Affective Disorder 9 41 0.062
172
SPS057 Spasticity 41 0.062
173
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.062
174
c SPS099 Spastic Paraplegia 42, Autosomal Dominant 40 0.062
175
ALL014 Allergic Encephalomyelitis 39 0.062
176
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.062
177
c PRG020 Paragangliomas 3 38 0.062
178
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.062
179
c MJR022 Major Affective Disorder 8 38 0.062
180
MCP033 Mucopolysaccharidoses 38 0.062
181
BTN004 Biotin Deficiency 38 0.062
182
ATX010 Ataxia Neuropathy Spectrum 38 0.062
183
MLN011 Malonyl-Coa Decarboxylase Deficiency 37 0.062
184
ALR002 Al-Raqad Syndrome 34 0.062
185
GNT167 Genetic Obesity 34 0.062
186
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 33 0.062
187
c FTL070 Fetal Akinesia Deformation Sequence 2 33 0.062
188
c RTN177 Retinitis Pigmentosa 73 32 0.062
189
ACT064 Acute Necrotizing Encephalitis 32 0.062
190
ANP008 Anaplastic Oligoastrocytoma 30 0.062
191
HYM001 Hymenolepiasis 29 0.062
192
PST092 Posttransplant Acute Limbic Encephalitis 29 0.062
193
MST020 Mast Cell Activation Syndrome 27 0.062
194
P SPS012 Spastic Paraplegia 3a 26 0.062
195
FTL073 Fetal Anticonvulsant Syndrome 26 0.062
196
BLD137 Blood Group--Ahonen 19 0.062
Content
Loading form....