Search results for slc25a20

23 hits were found for slc25a20

# Family MCID Name MIFTS Score
1
CRN041 Carnitine-Acylcarnitine Translocase Deficiency 51 7.908
2
HYP056 Hypoglycemia 66 4.563
3
P CRD119 Cardiac Arrest 67 3.989
4
P MYP004 Myopathy 70 2.821
5
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 2.821
6
MTC005 Mitochondrial Metabolism Disease 49 2.821
7
c ATR087 Atrial Standstill 1 75 2.067
8
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 68 1.995
9
CRN296 Carnitine Palmitoyltransferase Ii Deficiency, Infantile 65 1.995
10
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 64 1.995
11
CRN239 Carnitine Deficiency, Systemic Primary 62 1.995
12
MTC027 Mitochondrial Trifunctional Protein Deficiency 58 1.995
13
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 58 1.995
14
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 1.995
15
HYP774 Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome 55 1.995
16
CMB040 Combined D-2- and L-2-Hydroxyglutaric Aciduria 40 1.995
17
CMB019 Combined Oxidative Phosphorylation Deficiency 8 35 1.995
18
MTB016 Metabolic Myopathy 32 1.995
19
GTP001 Gait Apraxia 31 1.995
20
HPT022 Hepatoblastoma 56 0.087
21
P ACT008 Actinic Keratosis 53 0.087
22
KRT009 Keratosis 51 0.087
23
c INF145 Infantile Liver Failure Syndrome 1 50 0.087
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