Logo
Unionpedia
Communication
Get it on Google Play
New! Download Unionpedia on your Androidâ„¢ device!
Download
Faster access than browser!
 

3-Methylglutaconic aciduria and List of OMIM disorder codes

Shortcuts: Differences, Similarities, Jaccard Similarity Coefficient, References.

Difference between 3-Methylglutaconic aciduria and List of OMIM disorder codes

3-Methylglutaconic aciduria vs. List of OMIM disorder codes

3-Methylglutaconic aciduria (MGA) is any of at least five metabolic disorders that impair the body's ability to make energy in the mitochondria. This is a list of disorder codes in the Online Mendelian Inheritance in Man (OMIM) database.

Similarities between 3-Methylglutaconic aciduria and List of OMIM disorder codes

3-Methylglutaconic aciduria and List of OMIM disorder codes have 6 things in common (in Unionpedia): Barth syndrome, DNAJC19, Methylglutaconyl-CoA hydratase, Online Mendelian Inheritance in Man, OPA3, Tafazzin.

Barth syndrome

Barth syndrome (BTHS), also known as 3-Methylglutaconic aciduria type II, is an X-linked genetic disorder.

3-Methylglutaconic aciduria and Barth syndrome · Barth syndrome and List of OMIM disorder codes · See more »

DNAJC19

Mitochondrial import inner membrane translocase subunit TIM14 is an enzyme that in humans is encoded by the DNAJC19 gene on chromosome 3.

3-Methylglutaconic aciduria and DNAJC19 · DNAJC19 and List of OMIM disorder codes · See more »

Methylglutaconyl-CoA hydratase

3-Methylglutaconyl-CoA hydratase, also known as MG-CoA hydratase and AUH, is an enzyme encoded by the AUH gene on chromosome 19.

3-Methylglutaconic aciduria and Methylglutaconyl-CoA hydratase · List of OMIM disorder codes and Methylglutaconyl-CoA hydratase · See more »

Online Mendelian Inheritance in Man

Online Mendelian Inheritance in Man (OMIM) is a continuously updated catalog of human genes and genetic disorders and traits, with a particular focus on the gene-phenotype relationship.

3-Methylglutaconic aciduria and Online Mendelian Inheritance in Man · List of OMIM disorder codes and Online Mendelian Inheritance in Man · See more »

OPA3

Optic atrophy 3 protein is a protein that in humans is encoded by the OPA3 gene.

3-Methylglutaconic aciduria and OPA3 · List of OMIM disorder codes and OPA3 · See more »

Tafazzin

Tafazzin is a protein that in humans is encoded by the TAZ gene.

3-Methylglutaconic aciduria and Tafazzin · List of OMIM disorder codes and Tafazzin · See more »

The list above answers the following questions

3-Methylglutaconic aciduria and List of OMIM disorder codes Comparison

3-Methylglutaconic aciduria has 23 relations, while List of OMIM disorder codes has 2403. As they have in common 6, the Jaccard index is 0.25% = 6 / (23 + 2403).

References

This article shows the relationship between 3-Methylglutaconic aciduria and List of OMIM disorder codes. To access each article from which the information was extracted, please visit:

Hey! We are on Facebook now! »