ICDcodes.org
FY2027

P59.20Neonatal jaundice from unspecified hepatocellular damage

BillableUnspecifiedMCC

Is P59.20 billable?

Yes, but P59.20 is an unspecified code. P59.20 is a valid, billable ICD-10-CM code for encounters from October 1, 2026 through September 30, 2027. However, P59.20 is an unspecified or catch-all code. Payers apply additional scrutiny to unspecified codes and many deny them when the medical record supports a more specific option, so check the documentation before selecting P59.20 — the more specific alternatives are listed below.

P59.20 at a glance

CodeP59.20
DescriptionNeonatal jaundice from unspecified hepatocellular damage
BillableYes
Code setICD-10-CM FY2027
Valid for encountersOctober 1, 2026 – September 30, 2027

Which MS-DRGs does P59.20 group to?

P59.20 sits in MDC 15 and helps define the logic of 1 MS-DRG (version 44, FY2027). Which one a stay actually groups to also depends on procedures and secondary diagnoses.

  • 791Prematurity with Major Problemsmedical

As a secondary diagnosis, P59.20 is a major complication or comorbidity (MCC), which can move a stay into a higher-paying DRG.

How is P59.20 listed in the Alphabetic Index?

These are the routes through the Alphabetic Index that lead to P59.20. They show the wording a clinician may have documented, which often differs from the Tabular description.

  • Jaundicenewborndue to or associated withhepatocellular damage (yellow)
  • Newbornjaundicedue tohepatocellular damage (infant) (liveborn) (singleton)

Excludes1 — never code together — inherited from P50-P61

The conditions below can never be reported together with P59.20 on the same claim. An Excludes1 note means the two conditions cannot occur in the same patient, so reporting both is a coding error.

  • congenital stenosis and stricture of bile ducts (Q44.3)
  • Crigler-Najjar syndrome (E80.5)
  • Dubin-Johnson syndrome (E80.6)
  • Gilbert syndrome (E80.4)
  • hereditary hemolytic anemias (D55-D58)

Excludes1 — never code together — inherited from P59

The conditions below can never be reported together with P59.20 on the same claim. An Excludes1 note means the two conditions cannot occur in the same patient, so reporting both is a coding error.

  • jaundice due to inborn errors of metabolism (E70-E88)
  • kernicterus (P57.-)

Excludes1 — never code together — inherited from P59.2

The conditions below can never be reported together with P59.20 on the same claim. An Excludes1 note means the two conditions cannot occur in the same patient, so reporting both is a coding error.

  • congenital viral hepatitis (P35.3)

Excludes2 — not included here — inherited from Chapter 16

The conditions below are not part of P59.20, but a patient may have both at the same time. When documentation supports it, P59.20 and the excluded code may both be reported.

  • congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
  • endocrine, nutritional and metabolic diseases (E00-E88)
  • injury, poisoning and certain other consequences of external causes (S00-T88)
  • neoplasms (C00-D49)
  • tetanus neonatorum (A33)

How long has P59.20 existed?

P59.20 has been in ICD-10-CM since at least FY2016, the earliest fiscal year on record here.

Derived from the official order files for FY2016–FY2026. FY2017 and FY2020 publish no order file, so those years are not covered.

Which conditions are coded to P59.20?

What other codes are in the P59.2 family? (1)