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ICD-10 H31.2 - Hereditary choroidal dystrophy

H31.2

ICD-10 Not billable

Hereditary choroidal dystrophy

Specifically for this code:
  • hyperornithinemia (E72.4)
  • ornithinemia (E72.4)
From Chapter 7:
  • certain conditions originating in the perinatal period (P04-P96)
  • certain infectious and parasitic diseases (A00-B99)
  • complications of pregnancy, childbirth and the puerperium (O00-O9A)
  • congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
  • diabetes mellitus related eye conditions (E09.3-, E10.3-, E11.3-, E13.3-)
  • endocrine, nutritional and metabolic diseases (E00-E88)
  • injury (trauma) of eye and orbit (S05.-)
  • injury, poisoning and certain other consequences of external causes (S00-T88)
  • neoplasms (C00-D49)
  • symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
  • syphilis related eye disorders (A50.01, A50.3-, A51.43, A52.71)
From Chapter 7:
  • Use an external cause code following the code for the eye condition, if applicable, to identify the cause of the eye condition
H31.2 is a "category code," which means it's non-billable. Billable codes require more specificity. Use the list below to navigate to codes that are more specific:
10
H31.20
Hereditary choroidal dystrophy, unspecified
Billable
10
H31.21
Choroideremia
Billable
10
H31.22
Choroidal dystrophy (central areolar) (generalized) (peripapillary)
Billable
10
H31.23
Gyrate atrophy, choroid
Billable
10
H31.29
Other hereditary choroidal dystrophy
Billable
      
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