kodex

Kodex

G11.3

Cerebellar ataxia with defective DNA repair

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Hierarchy

  • G00-G99 Diseases of the nervous system (G00-G99)
    • G10-G14 Systemic atrophies primarily affecting the central nervous system (G10-G14)
      • G11 Hereditary ataxia
        • G11.0 Congenital nonprogressive ataxia
        • G11.1 Early-onset cerebellar ataxia
        • G11.2 Late-onset cerebellar ataxia
        • G11.3 Cerebellar ataxia with defective DNA repair
        • G11.4 Hereditary spastic paraplegia
        • G11.8 Other hereditary ataxias
        • G11.9 Hereditary ataxia, unspecified

Inclusion Terms

G11.3

  • Ataxia telangiectasia [Louis-Bar]

Excludes 2

G11.3

  • Cockayne's syndrome (Q87.19)
    • Q87.19 Other congenital malformation syndromes predominantly associated with short stature
  • other disorders of purine and pyrimidine metabolism (E79.-)
    • E79 Disorders of purine and pyrimidine metabolism
  • Q82.1 Xeroderma pigmentosum

G11

  • G80 Cerebral palsy
  • G60 Hereditary and idiopathic neuropathy
  • E70-E88 Metabolic disorders (E70-E88)

G00-G99

  • certain conditions originating in the perinatal period (P04-P96)
  • A00-B99 Certain infectious and parasitic diseases (A00-B99)
  • complications of pregnancy, childbirth and the puerperium (O00-O9A)
    • O00-O9A Pregnancy, childbirth and the puerperium (O00-O9A)
  • congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
    • Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
  • endocrine, nutritional and metabolic diseases (E00-E88)
  • S00-T88 Injury, poisoning and certain other consequences of external causes (S00-T88)
  • C00-D49 Neoplasms (C00-D49)
  • symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)