- Q87.89 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2024 edition of ICD-10-CM Q87.89 became effective on October 1, 2022.
- This is the American ICD-10-CM version of Q87.89 – other international versions of ICD-10 Q87.89 may differ.
ICD-10-CM Q87.89 is grouped within Diagnostic Related Group(s):
- 564 Other musculoskeletal system and connective tissue diagnoses with mcc
- 565 Other musculoskeletal system and connective tissue diagnoses with cc
- 566 Other musculoskeletal system and connective tissue diagnoses without cc/mcc
Applicable To
- Laurence-Moon (-Bardet)-Biedl syndrome
Code History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2016 (effective 10/1/2015): No change
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- 2024 (effective 10/1/2022): No change
Diagnosis Index entries containing back-references to Q87.89:
- basal cell nevus > Syndrome
- Birt-Hogg-Dube syndrome > Syndrome
- cardiofaciocutaneous > Syndrome
- congenital > Syndrome
- affecting multiple systems NEC > congenital Q87.89
- muscular hypertrophy-cerebral > congenital Q87.89
- Glass > Syndrome
- Gorlin\’s > Syndrome
- web > popliteal I77.89
- SATB2-associated > Syndrome
- popliteal syndrome > Web, webbed (congenital)