3 result found:

Xeroderma pigmentosum
ICD-10-CM Diagnosis Code Q82.1

Xeroderma pigmentosum

    2016 2017 2018 2019 2020 2021 Billable/Specific Code POA Exempt
Cerebellar ataxia with defective DNA repair
Ataxia telangiectasia syndrome; Cockayne's syndrome (Q87.19); other disorders of purine and pyrimidine metabolism (E79.-); xeroderma pigmentosum (Q82.1); Ataxia telangiectasia [Louis-Bar]
ICD-10-CM Diagnosis Code G11.3

Cerebellar ataxia with defective DNA repair

    2016 2017 2018 2019 2020 2021 Billable/Specific Code
Applicable To
  • Ataxia telangiectasia [Louis-Bar]
Type 2 Excludes
  • Cockayne's syndrome (Q87.19)
  • other disorders of purine and pyrimidine metabolism (E79.-)
  • xeroderma pigmentosum (Q82.1)
Disorders of purine and pyrimidine metabolism
Ataxia-telangiectasia (Q87.19); Bloom's syndrome (Q82.8); Cockayne's syndrome (Q87.19); calculus of kidney (N20.0); combined immunodeficiency disorders (D81.-); Fanconi's anemia (D61.09); gout (M1A.-, M10.-); orotaciduric anemia (D53.0); progeria (E34.8); Werner's syndrome (E34.8); xeroderma pigmentosum (Q82.1)
ICD-10-CM Diagnosis Code E79
  • E79 Disorders of purine and pyrimidine metabolism...
    • E79.0 Hyperuricemia without signs of inflammatory a...
    • E79.1 Lesch-Nyhan syndrome
    • E79.2 Myoadenylate deaminase deficiency
    • E79.8 Other disorders of purine and pyrimidine meta...
    • E79.9 Disorder of purine and pyrimidine metabolism,...