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3-Methylglutaconic aciduria

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3-Methylglutaconic aciduria (MGA) is used to describe at least five disorders that impair the body's ability to make energy in the mitochondria. [1]

18 relations: Amino acid, Apoptosis, Barth syndrome, Canada, Chromosome, DNAJC19, Dominance (genetics), Iraq, Jews, Locus (genetics), Methylglutaconyl-CoA hydratase, Mitochondrion, Online Mendelian Inheritance in Man, OPA3, Saguenay–Lac-Saint-Jean, Speech delay, Tafazzin, 3-Methylglutaconic acid.

Amino acid

Amino acids are biologically important organic compounds containing amine (-NH2) and carboxylic acid (-COOH) functional groups, usually along with a side-chain specific to each amino acid.

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Apoptosis (from Ancient Greek ἀπό apo, "by, from, of, since, than" and πτῶσις ptōsis, "fall") is the process of programmed cell death that may occur in multicellular organisms.

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Barth syndrome

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

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Canada is a country, consisting of ten provinces and three territories, in the northern part of the continent of North America.

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A chromosome (''chromo-'' + ''-some'') is a packaged and organized structure containing most of the DNA of a living organism.

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

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Dominance (genetics)

Dominance in genetics is a relationship between alleles of one gene, in which the effect on phenotype of one allele masks the contribution of a second allele at the same locus.

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Iraq (or; العراق, Kurdish: Êraq), officially the Republic of Iraq (Arabic: جمهورية العراق; كۆماری عێراق), is a country in Western Asia.

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The Jews (יְהוּדִים ISO 259-3, Israeli pronunciation), also known as the Jewish people, are an ethnoreligious and ethno-cultural group descended from the Israelites of the Ancient Near East and originating from the historical kingdoms of Israel and Judah.

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Locus (genetics)

A locus (plural loci) is the specific location or position of a gene, DNA sequence, on a chromosome, in the field of genetics.

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Methylglutaconyl-CoA hydratase

3-methylglutaconyl-CoA hydratase (also known as AUH) is an enzyme encoded by the AUH gene on chromosome 19.

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The mitochondrion (plural mitochondria) is a double membrane-bound organelle found in most eukaryotic cells.

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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.

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

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Saguenay–Lac-Saint-Jean is a region in Quebec, Canada.

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Speech delay

Speech delay, also known as alalia, refers to a delay in the development or use of the mechanisms that produce speech.

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

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3-Methylglutaconic acid

3-Methylglutaconic acid is a glutarate which builds up in the urine in 3-methylglutaconic aciduria or 3-hydroxy-3-methylglutaric aciduria.

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Redirects here:

3 methylglutaconyl coa hydratase deficiency, 3-Methylglutaconic acidemia, 3-Methylglutaconic aciduria type 1, 3-Methylglutaconic aciduria type 3, 3-Methylglutaconic aciduria type 4, 3-Methylglutaconic aciduria type 5, 3-Methylglutaconic aciduria type I, 3-Methylglutaconic aciduria type III, 3-Methylglutaconic aciduria type IV, 3-Methylglutaconic aciduria type V, 3-Methylglutaconyl-CoA Hydratase Deficiency, 3-methyl glutaconic aciduria, 3-methylglutaconic aciduria, 3MGA, Costeff syndrome, MGA type 1, MGA type 3, MGA type 4, MGA type 5, MGA type I, MGA type III, MGA type IV, MGA type V.


[1] https://en.wikipedia.org/wiki/3-Methylglutaconic_aciduria

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