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Metadata
ID SO:0002165
Name trinucleotide_repeat_expansion
Parent Relationships

is_a short_tandem_repeat_expansion

Related Diseases

has material basis in

  • fragile X-associated tremor/ataxia syndrome
  • spinocerebellar ataxia type 1
  • neuronal intranuclear inclusion disease
  • essential tremor 6
  • oculopharyngodistal myopathy 1
  • oculopharyngodistal myopathy 2
  • oculopharyngodistal myopathy 3
  • oculopharyngodistal myopathy 4
  • amyotrophic lateral sclerosis type 28
  • myotonic dystrophy type 1
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