kodex

Kodex

ICD-10-CM
Code

G13.2

Systemic atrophy primarily affecting the central nervous system in myxedema

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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)
      • G13 Systemic atrophies primarily affecting central nervous system in diseases classified elsewhere
        • G13.0 Paraneoplastic neuromyopathy and neuropathy
        • G13.1 Other systemic atrophy primarily affecting central nervous system in neoplastic disease
        • G13.2 Systemic atrophy primarily affecting the central nervous system in myxedema
        • G13.8 Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere

Code First

G13.2

  • underlying disease, such as:
  • hypothyroidism (E03.-)
    • E03 Other hypothyroidism
  • myxedematous congenital iodine deficiency (E00.1)
    • E00.1 Congenital iodine-deficiency syndrome, myxedematous type

Excludes 2

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)

Related Terms