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.
Inclusion 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
P09.2 does not map to an HCC and does not risk-adjust under CMS-HCC V28. That is normal — most ICD-10 codes do not. It still needs to be coded correctly; it just will not move a RAF score.
How P09.2 is indexed
Coders do not find codes by browsing the tabular list — they look them up in the alphabetic index, under the word the physician wrote. These are the index entries that lead here, so you can see which chart wordings map to P09.2.
- 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
Related codes at this level
Codes that share P09. If P09.2 is not quite right, the correct code is usually one of these.
- 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
Questions about P09.2
- Is P09.2 a billable ICD-10-CM code?
- Yes. P09.2 is a billable, specific ICD-10-CM code and is valid for submission on a claim.
- Where does P09.2 sit in the tabular list?
- Certain conditions originating in the perinatal period (P00-P96), in the block Abnormal findings on neonatal screening (P09).