Search results for acetyl-coa

51 hits were found for acetyl-coa

# Family MCID Name MIFTS Score
1
ACT086 Acetyl-Coa Carboxylase Deficiency 16 12.106
2
c MCP045 Mucopolysaccharidosis, Type Iiic 35 9.343
3
ACT239 Acetyl-Coa Acetyltransferase-2 Deficiency 17 9.343
4
MTH074 Methionine Adenosyltransferase I/iii Deficiency 43 7.562
5
ALP077 Alpha-Methylacetoacetic Aciduria 41 7.562
6
HYP003 Hypermethioninemia 35 5.347
7
MTH011 Methionine Adenosyltransferase Deficiency 17 5.347
8
NCT004 N Acetyltransferase Deficiency 15 5.347
9
P BRS047 Breast Cancer 100 0.228
10
P PNC044 Pancreatitis 64 0.180
11
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.140
12
P THY032 Thyroiditis 56 0.140
13
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.140
14
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.140
15
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.140
16
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.140
17
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.140
18
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.140
19
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.140
20
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.140
21
P PRS040 Prostate Cancer 88 0.114
22
MLT018 Multiple Carboxylase Deficiency 45 0.114
23
c HYP793 Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 40 0.114
24
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.081
25
GST053 Gastric Cancer 84 0.081
26
P HPT021 Hepatitis 75 0.081
27
GLB002 Glioblastoma 74 0.081
28
P NRB001 Neuroblastoma 73 0.081
29
P ADN016 Adenocarcinoma 71 0.081
30
P MYP004 Myopathy 69 0.081
31
P ANR048 Aniridia 1 68 0.081
32
PNC041 Pancreatic Ductal Adenocarcinoma 67 0.081
33
ADR054 Adrenocortical Carcinoma, Hereditary 63 0.081
34
P MCP040 Mucopolysaccharidosis-Plus Syndrome 61 0.081
35
PRS047 Prostatitis 59 0.081
36
ALL026 Allergic Hypersensitivity Disease 59 0.081
37
P LTR001 Lateral Sclerosis 58 0.081
38
WST005 West Nile Virus 58 0.081
39
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 54 0.081
40
PRP016 Paraplegia 53 0.081
41
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 52 0.081
42
NRN002 Neuronitis 43 0.081
43
SPS057 Spasticity 41 0.081
44
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.081
45
c SPS099 Spastic Paraplegia 42, Autosomal Dominant 35 0.081
46
MLN011 Malonyl-Coa Decarboxylase Deficiency 32 0.081
47
c SPS021 Spastic Paraplegia 10 26 0.081
48
ANR038 Anorexia Nervosa 1 21 0.081
49
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.081
50
BLD137 Blood Group--Ahonen 17 0.081
51
LTH048 L-Threonine Dehydrogenase, Pseudogene 10 0.081
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