trinucleotide repeat disorder (Q21677): Difference between revisions
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Created a new Item: trinucleotide repeat disorder, a genetic disorders caused by trinucleotide repeat expansion, a kind of mutation where trinucleotide repeats in certain genes or introns exceed the normal, stable threshold, which differs per gene |
Created claim: subclass of (P1): neurodegeneration (Q12703) |
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| Property / subclass of | |||
| Property / subclass of: neurodegeneration / rank | |||
Normal rank | |||
Revision as of 20:55, 2 April 2024
a genetic disorders caused by trinucleotide repeat expansion, a kind of mutation where trinucleotide repeats in certain genes or introns exceed the normal, stable threshold, which differs per gene
- trinucleotide repeat expansion disorders
- triplet repeat expansion disorders
- codon reiteration disorders
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | trinucleotide repeat disorder |
a genetic disorders caused by trinucleotide repeat expansion, a kind of mutation where trinucleotide repeats in certain genes or introns exceed the normal, stable threshold, which differs per gene |
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