Search results for acat2

85 hits were found for acat2

# Family MCID Name MIFTS Score
1
ACT239 Acetyl-Coa Acetyltransferase-2 Deficiency 20 49.905
2
ALP077 Alpha-Methylacetoacetic Aciduria 52 9.135
3
SCH078 Schimmelpenning-Feuerstein-Mims Syndrome 61 9.135
4
c HYP836 Hypercholesterolemia, Familial, 1 73 8.851
5
ATH013 Atherosclerosis Susceptibility 63 6.593
6
P HYP750 Hypertriglyceridemia, Familial 62 4.379
7
NNL005 Non-Alcoholic Fatty Liver Disease 63 4.238
8
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 3.603
9
47X002 47,xyy 48 3.361
10
FTT001 Fatty Liver Disease 62 3.195
11
P BRS047 Breast Cancer 98 3.157
12
P CLR023 Colorectal Cancer 100 3.107
13
c GLL024 Gallbladder Disease 1 52 3.040
14
P CRN300 Coronary Heart Disease 1 73 2.606
15
FML035 Familial Hyperlipidemia 55 2.488
16
c MTR020 Maturity-Onset Diabetes of the Young, Type 3 54 2.362
17
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 2.362
18
RNL114 Renal Cell Carcinoma, Nonpapillary 80 2.362
19
CLR030 Clear Cell Renal Cell Carcinoma 54 2.362
20
P HRT032 Heart Disease 81 2.362
21
NRL016 Neural Tube Defects 81 2.224
22
ART140 Arteries, Anomalies of 53 2.138
23
LPP008 Lipoprotein Quantitative Trait Locus 65 2.138
24
c PRG020 Paragangliomas 3 39 2.138
25
ISC004 Ischemia 61 1.824
26
GLM045 Glioma 63 1.659
27
AGN016 Aging 54 1.290
28
LPD008 Lipid Metabolism Disorder 62 1.290
29
P PNC035 Pancreatic Cancer 86 1.196
30
HMC014 Homocysteinemia 52 1.117
32
CLB022 Coloboma, Ocular, Autosomal Recessive 28 1.117
33
c CHR684 Chronic Kidney Disease 69 1.117
34
P KDN018 Kidney Disease 72 1.117
35
P NPH012 Nephrotic Syndrome 60 1.117
36
P GLM040 Glioma Susceptibility 1 71 1.109
37
P ALZ034 Alzheimer Disease 87 0.912
38
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.912
39
c MST023 Mesothelioma, Malignant 56 0.912
40
CLT003 Colitis 63 0.912
41
LYS012 Lysosomal Acid Lipase Deficiency 65 0.912
42
c PCH010 Pachyonychia Congenita 3 43 0.912
43
c HPT073 Hepatitis C Virus 71 0.912
44
c LNG109 Lung Cancer Susceptibility 1 26 0.912
45
RPD005 Rapidly Involuting Congenital Hemangioma 46 0.912
46
ULC004 Ulcerative Colitis 74 0.912
47
c HPT001 Hepatitis C 62 0.912
48
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.912
49
CLN015 Colon Adenocarcinoma 65 0.912
50
P BNG032 Benign Mesothelioma 53 0.912
51
PLY100 Polyploidy 36 0.645
52
HMZ003 Homozygous Familial Hypercholesterolemia 60 0.645
53
LCT022 Lecithin:cholesterol Acyltransferase Deficiency 58 0.645
54
P AST005 Asthma 76 0.645
55
PPL052 Papillomatosis, Confluent and Reticulated 34 0.645
56
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.645
57
P PRK057 Parkinson Disease, Late-Onset 80 0.645
58
CYS001 Cystic Fibrosis 78 0.645
59
ATS010 Autosomal Recessive Disease 42 0.645
60
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.645
61
FST003 Fasting Insulin Level Quantitative Trait Locus 1 6 0.645
62
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 0.645
63
DWN001 Down Syndrome 70 0.645
64
OST159 Osteogenic Sarcoma 66 0.645
65
c TYP009 Type 2 Diabetes Mellitus 92 0.645
66
P NRB001 Neuroblastoma 66 0.645
67
GLL048 Glial Tumor 52 0.645
68
GLB002 Glioblastoma 67 0.645
69
HYP082 Hypopharynx Cancer 47 0.645
70
P LNG064 Lung Cancer Susceptibility 3 70 0.645
71
P LTR001 Lateral Sclerosis 58 0.645
72
MLG169 Malignant Astrocytoma 57 0.645
73
c INH020 Inherited Metabolic Disorder 48 0.645
74
GST045 Gastroenteritis 58 0.645
75
c FML021 Familial Hypercholesterolemia 72 0.645
76
CHL068 Cholestasis 61 0.645
77
HYP060 Hyperinsulinism 54 0.645
78
CHR178 Chromosomal Triplication 34 0.645
79
P LKM062 Leukemia, Acute Lymphoblastic 69 0.551
80
c GLM047 Glioma Susceptibility 3 33 0.464
81
c MSM022 Mismatch Repair Cancer Syndrome 1 70 0.464
82
c GLM025 Glioma Susceptibility 2 30 0.464
83
c GLM043 Glioma Susceptibility 9 30 0.464
84
MNN043 Meningioma, Familial 79 0.464
85
P OLG002 Oligodendroglioma 66 0.464
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