Search results for acetyl-coa

92 hits were found for acetyl-coa

# Family MCID Name MIFTS Score
1
ACT086 Acetyl-Coa Carboxylase Deficiency 15 13.176
2
ACT239 Acetyl-Coa Acetyltransferase-2 Deficiency 18 11.982
3
c MCP045 Mucopolysaccharidosis, Type Iiic 34 9.317
4
ALP077 Alpha-Methylacetoacetic Aciduria 45 7.526
5
NCT004 N Acetyltransferase Deficiency 22 5.739
6
HYP003 Hypermethioninemia 40 5.322
7
MTH074 Methionine Adenosyltransferase I/iii Deficiency 39 5.322
8
MTH011 Methionine Adenosyltransferase Deficiency 16 5.322
9
P BRS047 Breast Cancer 100 0.209
10
c APL023 Aplasia Cutis Congenita, Nonsyndromic 40 0.209
11
c FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.139
12
c MCP001 Mucopolysaccharidosis Iii 63 0.121
13
P HPT023 Hepatocellular Carcinoma 96 0.098
14
P PRS040 Prostate Cancer 93 0.098
15
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 92 0.098
16
GLB002 Glioblastoma 74 0.098
17
P ENC018 Encephalopathy 65 0.098
18
RNL114 Renal Cell Carcinoma, Nonpapillary 63 0.098
19
HYP266 Hypoxia 63 0.098
20
MLT018 Multiple Carboxylase Deficiency 43 0.098
21
c HYP793 Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 42 0.098
22
P CLR023 Colorectal Cancer 99 0.070
23
c AMY091 Amyotrophic Lateral Sclerosis 1 90 0.070
24
CYS001 Cystic Fibrosis 82 0.070
25
P PNC035 Pancreatic Cancer 82 0.070
26
SQM013 Squamous Cell Carcinoma, Head and Neck 82 0.070
27
GST053 Gastric Cancer 78 0.070
28
P NRF023 Neurofibromatosis, Type Ii 75 0.070
29
P HPT021 Hepatitis 73 0.070
30
P GRF003 Graft-Versus-Host Disease 71 0.070
31
P BLD134 Bladder Cancer 70 0.070
32
P ADN016 Adenocarcinoma 70 0.070
33
ANR007 Anorexia Nervosa 68 0.070
34
P MYC084 Mycobacterium Tuberculosis 1 67 0.070
35
ISC004 Ischemia 67 0.070
36
P ATS364 Autism 67 0.070
37
FTT001 Fatty Liver Disease 66 0.070
38
LPD008 Lipid Metabolism Disorder 65 0.070
39
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.070
40
P MYP004 Myopathy 64 0.070
41
HYP066 Hyperglycemia 64 0.070
42
GLB015 Glioblastoma Multiforme 64 0.070
43
P ANR048 Aniridia 1 64 0.070
44
ACN002 Acanthosis Nigricans 64 0.070
45
CYT008 Cytomegalovirus Infection 62 0.070
46
AND002 Androgen Insensitivity Syndrome 61 0.070
47
P TRC086 Trichohepatoenteric Syndrome 1 60 0.070
48
ATH013 Atherosclerosis Susceptibility 60 0.070
49
P MCP040 Mucopolysaccharidosis-Plus Syndrome 60 0.070
50
P LTR001 Lateral Sclerosis 60 0.070
51
P HYP750 Hypertriglyceridemia, Familial 58 0.070
52
c MCR113 Microvascular Complications of Diabetes 3 58 0.070
53
SQM006 Squamous Cell Carcinoma 58 0.070
54
c ACT135 Acute Graft Versus Host Disease 58 0.070
55
P AXN002 Axenfeld-Rieger Syndrome 57 0.070
56
ADR016 Adrenal Cortical Carcinoma 57 0.070
57
c GLC092 Glaucoma, Primary Open Angle 57 0.070
58
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 56 0.070
59
PRP016 Paraplegia 54 0.070
60
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 54 0.070
61
NNL002 Nonalcoholic Steatohepatitis 54 0.070
62
PNC041 Pancreatic Ductal Adenocarcinoma 54 0.070
63
P OPN001 Open-Angle Glaucoma 53 0.070
64
P PLG001 Pelger-Huet Anomaly 52 0.070
65
RNL077 Renal Fibrosis 51 0.070
66
FSH001 Fish-Eye Disease 50 0.070
67
CTY001 Cat Eye Syndrome 50 0.070
68
TRP008 Tropical Calcific Pancreatitis 50 0.070
69
c RTN177 Retinitis Pigmentosa 73 48 0.070
70
P APL006 Aplasia Cutis Congenita 48 0.070
71
P BRB001 Beriberi 46 0.070
72
c MCR120 Microvascular Complications of Diabetes 7 46 0.070
73
CRP032 Corpus Callosum, Agenesis of 45 0.070
74
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 44 0.070
75
c MCR130 Microvascular Complications of Diabetes 6 43 0.070
76
c MCR133 Microvascular Complications of Diabetes 4 43 0.070
77
ALL014 Allergic Encephalomyelitis 43 0.070
78
ALR002 Al-Raqad Syndrome 40 0.070
79
c PRS136 Prostate Cancer, Hereditary, 6 40 0.070
80
ATX010 Ataxia Neuropathy Spectrum 39 0.070
81
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 38 0.070
82
c SPS099 Spastic Paraplegia 42, Autosomal Dominant 38 0.070
83
c PRS130 Prostate Cancer, Hereditary, 8 37 0.070
84
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 36 0.070
85
MLN011 Malonyl-Coa Decarboxylase Deficiency 33 0.070
86
PPL052 Papillomatosis, Confluent and Reticulated 33 0.070
87
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 33 0.070
88
FRN020 Frontal Fibrosing Alopecia 33 0.070
89
NTR027 Neutrophil Actin Dysfunction 32 0.070
90
MYC071 Myoclonic-Atonic Epilepsy 31 0.070
91
P ACT232 Acute Necrotizing Encephalopathy 30 0.070
92
BLD137 Blood Group--Ahonen 24 0.070
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