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13 relations: Ataxin, Chromosome 9, Coenzyme Q10, Dihydrolipoamide dehydrogenase, Ferrochelatase, Frataxin-like domain, Friedreich's ataxia, List of genetic disorders, List of OMIM disorder codes, Mitosome, PMPCB, Trinucleotide repeat disorder, Triple-stranded DNA.
Ataxin
Ataxin is a type of nuclear protein.
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Chromosome 9
Chromosome 9 is one of the 23 pairs of chromosomes in humans.
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Coenzyme Q10
Coenzyme Q10, also known as ubiquinone, ubidecarenone, coenzyme Q, and abbreviated at times to CoQ10, CoQ, or Q10 is a coenzyme that is ubiquitous in animals and most bacteria (hence the name ubiquinone).
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Dihydrolipoamide dehydrogenase
Dihydrolipoamide dehydrogenase (DLD), also known as dihydrolipoyl dehydrogenase, mitochondrial, is an enzyme that in humans is encoded by the DLD gene.
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Ferrochelatase
Ferrochelatase (or protoporphyrin ferrochelatase) is an enzyme that is encoded by the FECH gene in humans.
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Frataxin-like domain
In molecular biology, the frataxin-like domain is a protein domain found in proteins including eukaryotic frataxin and bacterial CyaY.
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Friedreich's ataxia
Friedreich's ataxia is an autosomal recessive inherited disease that causes progressive damage to the nervous system.
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List of genetic disorders
The following is a list of genetic disorders and if known, type of mutation and the chromosome involved.
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List of OMIM disorder codes
This is a list of disorder codes in the Online Mendelian Inheritance in Man (OMIM) database.
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Mitosome
A mitosome is an organelle found in some unicellular eukaryotic organisms.
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PMPCB
Mitochondrial-processing peptidase subunit beta is an enzyme that in humans is encoded by the PMPCB gene.
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Trinucleotide repeat disorder
Trinucleotide repeat disorders (also known as trinucleotide repeat expansion disorders, triplet repeat expansion disorders or codon reiteration disorders) are a set of genetic disorders caused by trinucleotide repeat expansion, a kind of mutation where trinucleotide repeats in certain genes or intronsDavid W. Sanders & Clifford P. Brangwynne (2017), Nature, 546, 215–216 (08 June 2017) exceed the normal, stable threshold, which differs per gene.
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Triple-stranded DNA
Triple-stranded DNA is a DNA structure in which three oligonucleotides wind around each other and form a triple helix.
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