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 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.
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.
Barth syndrome (BTHS), also known as 3-Methylglutaconic aciduria type II, is an X-linked genetic disorder.
Canada is a country, consisting of ten provinces and three territories, in the northern part of the continent of North America.
A chromosome (''chromo-'' + ''-some'') is a packaged and organized structure containing most of the DNA of a living organism.
Mitochondrial import inner membrane translocase subunit TIM14 is an enzyme that in humans is encoded by the DNAJC19 gene on chromosome 3.
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.
Iraq (or; العراق, Kurdish: Êraq), officially the Republic of Iraq (Arabic: جمهورية العراق; كۆماری عێراق), is a country in Western Asia.
New!!: 3-Methylglutaconic aciduria and Iraq ·
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.
New!!: 3-Methylglutaconic aciduria and Jews ·
A locus (plural loci) is the specific location or position of a gene, DNA sequence, on a chromosome, in the field of genetics.
3-methylglutaconyl-CoA hydratase (also known as AUH) is an enzyme encoded by the AUH gene on chromosome 19.
The mitochondrion (plural mitochondria) is a double membrane-bound organelle found in most eukaryotic cells.
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.
Optic atrophy 3 protein is a protein that in humans is encoded by the OPA3 gene.
New!!: 3-Methylglutaconic aciduria and OPA3 ·
Saguenay–Lac-Saint-Jean is a region in Quebec, Canada.
Speech delay, also known as alalia, refers to a delay in the development or use of the mechanisms that produce speech.
Tafazzin is a protein that in humans is encoded by the TAZ gene.
3-Methylglutaconic acid is a glutarate which builds up in the urine in 3-methylglutaconic aciduria or 3-hydroxy-3-methylglutaric aciduria.
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.