Category
page 1Trinucleotide repeat disorders
Huntington's disease
rare neurodegenerative disorder of the central nervous system characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia
fragile X syndrome
congenital disorder of nervous system
Friedreich ataxia
Human disease
myotonic dystrophy
long term genetic disorder that affects muscle function
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
dentatorubral-pallidoluysian atrophy
congenital disorder of nervous system
spinocerebellar ataxia type 6
Human disease