Werner Syndrome
Xeroderma Pigmentosum, Variant Type
Bloom Syndrome
Vitelliform Macular Dystrophy
Fanconi Anemia, Complementation Group a
Xeroderma Pigmentosum, Complementation Group G
Huntington Disease
Cockayne Syndrome
Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia
Rothmund-Thomson Syndrome, Type 2
Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 1
Baller-Gerold Syndrome
Developmental and Epileptic Encephalopathy 75
Cockayne Syndrome B
Colorectal Cancer
Trichothiodystrophy
Sezary's Disease
Fuchs' Endothelial Dystrophy
Aplastic Anemia