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Explore conditions, clinical trials, and the organisations running them.

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Up to: Inborn errors of metabolism

DNA repair disease

A disease that has its basis in the disruption of DNA repair.

13 trials tagged with this condition →

  • Fanconi anemia 29 trials · 42 incl. sub-types Sub-types →
  • Mismatch repair cancer syndrome 5 trials · 36 incl. sub-types Sub-types →
  • Cockayne syndrome 6 trials Sub-types →
  • Xeroderma pigmentosum 4 trials · 6 incl. sub-types Sub-types →
  • Severe combined immunodeficiency due to DCLRE1C deficiency 3 trials
  • Karyomegalic interstitial nephritis 2 trials
  • Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 0 trials · 2 incl. sub-types Sub-types →
  • COFS syndrome 1 trial Sub-types →
  • Nijmegen breakage syndrome 1 trial
  • Nijmegen breakage syndrome-like disorder 0 trials
  • UV-sensitive syndrome 0 trials Sub-types →
  • Ataxia and polyneuropathy, adult-onset 0 trials
  • Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia 0 trials
  • Ataxia-telangiectasia-like disorder 1 0 trials
  • Ataxia-telangiectasia-like disorder 2 0 trials
  • Photosensitive trichothiodystrophy 0 trials Sub-types →

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