P09.2
P09.2: Abnormal findings on neonatal screening for congenital endocrine disease
Billable / specific codeICD-10-CM
P09.2 is a billable, specific ICD-10-CM code for abnormal findings on neonatal screening for congenital endocrine disease. It is valid for submission on a claim.
Check P09.2 with the rest of the claim: free scrubberInclusion terms
Alternative wordings a physician may use in the chart for this same code.
- Abnormal findings on neonatal screening for congenital adrenal hyperplasia
- Abnormal findings on neonatal screening for hypothyroidism screen
Risk adjustment
No CMS-HCC V28 category: this code does not change a RAF score.
Alphabetic index entries that lead here
- Abnormal, abnormality, abnormalities›neonatal screening›for›congenital adrenal hyperplasia
- Abnormal, abnormality, abnormalities›neonatal screening›for›congenital endocrine disease
- Abnormal, abnormality, abnormalities›neonatal screening›for›hypothyroidism
Code history
Unchanged in every release from FY2024 to FY2027.
Other codes under P09
- P09.1Abnormal findings on neonatal screening for inborn errors of metabolism
- P09.3Abnormal findings on neonatal screening for congenital hematologic disorders
- P09.4Abnormal findings on neonatal screening for cystic fibrosis
- P09.5Abnormal findings on neonatal screening for critical congenital heart disease
- P09.6Abnormal findings on neonatal hearing screening
- P09.8Other abnormal findings on neonatal screening
- P09.9Abnormal findings on neonatal screening, unspecified