MCID: MLT154
MIFTS: 14

Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type

Categories: Metabolic diseases, Neuronal diseases, Rare diseases

Aliases & Classifications for Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type

MalaCards integrated aliases for Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type:

Name: Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type 58
Glutaric Aciduria Type 2, Mild Type 58
Mad Deficiency, Mild Type 58
Madd, Mild Type 58

Classifications:

Orphanet: 58  
Rare neurological diseases
Inborn errors of metabolism


External Ids:

ICD10 via Orphanet 33 E71.3
Orphanet 58 ORPHA394532

Summaries for Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type

MalaCards based summary : Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type, also known as glutaric aciduria type 2, mild type, is related to acyl-coa dehydrogenase, short-chain, deficiency of and acyl-coa dehydrogenase, very long-chain, deficiency of. An important gene associated with Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type is ETFA (Electron Transfer Flavoprotein Subunit Alpha), and among its related pathways/superpathways is Metabolism.

Related Diseases for Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type

Graphical network of the top 20 diseases related to Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type:



Diseases related to Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type

Symptoms & Phenotypes for Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type

Drugs & Therapeutics for Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type

Search Clinical Trials , NIH Clinical Center for Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type

Genetic Tests for Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type

Anatomical Context for Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type

Publications for Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type

Variations for Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type

Expression for Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type

Search GEO for disease gene expression data for Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type.

Pathways for Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type

Pathways related to Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type according to GeneCards Suite gene sharing:

# Super pathways Score Top Affiliating Genes
1
Show member pathways
12.67 SLC25A32 FLAD1 ETFDH ETFB ETFA

GO Terms for Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type

Cellular components related to Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type according to GeneCards Suite gene sharing:

# Name GO ID Score Top Affiliating Genes
1 mitochondrion GO:0005739 9.35 SLC25A32 FLAD1 ETFDH ETFB ETFA
2 mitochondrial membrane GO:0031966 9.16 SLC25A32 ETFDH
3 mitochondrial matrix GO:0005759 8.92 FLAD1 ETFDH ETFB ETFA

Biological processes related to Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type according to GeneCards Suite gene sharing:

# Name GO ID Score Top Affiliating Genes
1 oxidation-reduction process GO:0055114 9.43 ETFDH ETFB ETFA
2 electron transport chain GO:0022900 9.33 ETFDH ETFB ETFA
3 respiratory electron transport chain GO:0022904 9.13 ETFDH ETFB ETFA
4 fatty acid beta-oxidation using acyl-CoA dehydrogenase GO:0033539 8.8 ETFDH ETFB ETFA

Molecular functions related to Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type according to GeneCards Suite gene sharing:

# Name GO ID Score Top Affiliating Genes
1 flavin adenine dinucleotide binding GO:0050660 8.96 ETFDH ETFA
2 electron transfer activity GO:0009055 8.8 ETFDH ETFB ETFA

Sources for Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
43 MeSH
44 MESH via Orphanet
45 MGI
48 NCI
49 NCIt
50 NDF-RT
53 NINDS
54 Novoseek
56 OMIM
57 OMIM via Orphanet
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
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