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 repeats in certain genes exceed the normal, stable, threshold, which differs per gene.
Trinucleotide repeat disorderAnticipation (genetics)Trinucleotide repeat expansionDynamic mutationATN1Huntington's diseaseHuntingtinMyotonic dystrophyNon-Mendelian inheritanceFragile X syndromeDentatorubral-pallidoluysian atrophyList of genetic disordersOculopharyngeal muscular dystrophyEhud ShapiroDynamical geneticsFragile X-associated tremor/ataxia syndromeAnita HardingNeurodegenerationSpinocerebellar ataxiaTandem repeat
Androgen receptorSpinal and bulbar muscular atrophyAtaxia telangiectasiaAndrogen insensitivity syndromeMild androgen insensitivity syndromeATXN2MED15Machado–Joseph diseaseNeuroacanthocytosis60S ribosomal protein L14FMR1Causes of autismCav2.1Ataxin 3Michael R. HaydenCNDP1MED12Insertion (genetics)ATXN2LHeritability of IQ
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