MCID: MLT154
MIFTS: 13

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 59
Glutaric Aciduria Type 2, Mild Type 59
Mad Deficiency, Mild Type 59
Madd, Mild Type 59

Classifications:



External Ids:

ICD10 via Orphanet 34 E71.3
Orphanet 59 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 chanarin-dorfman syndrome and riboflavin deficiency. 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

Diseases related to Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 chanarin-dorfman syndrome 9.4 ETFDH ETFB
2 riboflavin deficiency 8.9 FLAD1 ETFDH ETFA
3 multiple acyl-coa dehydrogenase deficiency 8.5 FLAD1 ETFDH ETFB ETFA
4 multiple acyl-coa dehydrogenase deficiency, severe neonatal type 8.5 FLAD1 ETFDH ETFB ETFA

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 9.33 ETFDH ETFB ETFA
2 electron transport chain GO:0022900 9.13 ETFDH ETFB ETFA
3 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 HGMD
31 HMDB
32 HPO
33 ICD10
34 ICD10 via Orphanet
35 ICD9CM
36 IUPHAR
37 KEGG
38 LifeMap
40 LOVD
42 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
54 NINDS
55 Novoseek
57 OMIM
58 OMIM via Orphanet
62 PubMed
64 QIAGEN
69 SNOMED-CT via HPO
70 TGDB
71 Tocris
72 UMLS
73 UMLS via Orphanet
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