DNA repair disease

Part of

Sub-types of DNA repair disease

• Fanconi anemia 29 trials · 42 incl. sub-types
  22 sub-types

  • Fanconi anemia complementation group D1 6 trials
  • Fanconi anemia complementation group A 4 trials
  • Fanconi anemia complementation group E 4 trials
  • Fanconi anemia complementation group N 2 trials
  • Fanconi anemia, complementation group S 2 trials
  • Fanconi anemia complementation group B 0 trials
  • Fanconi anemia complementation group C 0 trials
  • Fanconi anemia complementation group D2 0 trials
  • Fanconi anemia complementation group F 0 trials
  • Fanconi anemia complementation group G 0 trials
  • Fanconi anemia complementation group I 0 trials
  • Fanconi anemia complementation group J 0 trials
  • Fanconi anemia complementation group L 0 trials
  • Fanconi anemia complementation group O 0 trials
  • Fanconi anemia complementation group P 0 trials
  • Fanconi anemia complementation group Q 0 trials
  • Fanconi anemia complementation group R 0 trials
  • Fanconi anemia complementation group T 0 trials
  • Fanconi anemia complementation group U 0 trials
  • Fanconi anemia complementation group V 0 trials
  • Fanconi anemia, complementation group W 0 trials
  • Fanconi anemia, complementation group 10 0 trials
• Mismatch repair cancer syndrome 5 trials · 36 incl. sub-types
  4 sub-types

  • Mismatch repair cancer syndrome 1 34 trials
  • Mismatch repair cancer syndrome 2 0 trials
  • Mismatch repair cancer syndrome 3 0 trials
  • Mismatch repair cancer syndrome 4 0 trials
• Cockayne syndrome 6 trials
  4 sub-types

  • Cockayne spectrum with or without cerebrooculofacioskeletal syndrome 0 trials
  • Cockayne syndrome type 1 0 trials
  • Cockayne syndrome type 2 0 trials
  • Cockayne syndrome type 3 0 trials
• Xeroderma pigmentosum 4 trials · 6 incl. sub-types
  10 sub-types

  • Xeroderma pigmentosum group F 1 trial
  • Xeroderma pigmentosum variant type 1 trial
  • Xeroderma pigmentosum group A 0 trials
  • Xeroderma pigmentosum group B 0 trials
  • Xeroderma pigmentosum group C 0 trials
  • Xeroderma pigmentosum group D 0 trials
  • Xeroderma pigmentosum group E 0 trials
  • Xeroderma pigmentosum group G 0 trials
  • Xeroderma pigmentosum, autosomal dominant, mild 0 trials
  • Xeroderma pigmentosum, complementation group J 0 trials
• 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
  3 sub-types

  • Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2 2 trials
  • Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1 0 trials
  • Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3 0 trials
• COFS syndrome 1 trial
  5 sub-types

  • Cerebrooculofacioskeletal syndrome 1 0 trials
  • Cerebrooculofacioskeletal syndrome 2 0 trials
  • Cerebrooculofacioskeletal syndrome 3 0 trials
  • Cerebrooculofacioskeletal syndrome 4 0 trials
  • Xeroderma pigmentosum group G 0 trials
• Nijmegen breakage syndrome 1 trial
• Nijmegen breakage syndrome-like disorder 0 trials
• UV-sensitive syndrome 0 trials
  3 sub-types

  • UV-sensitive syndrome 1 0 trials
  • UV-sensitive syndrome 2 0 trials
  • UV-sensitive syndrome 3 0 trials
• 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
  3 sub-types

  • Trichothiodystrophy 1, photosensitive 0 trials
  • Trichothiodystrophy 2, photosensitive 0 trials
  • Trichothiodystrophy 3, photosensitive 0 trials