20162017201820192020202120222023Billable/Specific Code
- Q89.09 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2023 edition of ICD-10-CM Q89.09 became effective on October 1, 2022.
- This is the American ICD-10-CM version of Q89.09 – other international versions of ICD-10 Q89.09 may differ.
ICD-10-CM Q89.09 is grouped within Diagnostic Related Group(s):
- 814 Reticuloendothelial and immunity disorders with mcc
- 815 Reticuloendothelial and immunity disorders with cc
- 816 Reticuloendothelial and immunity disorders without cc/mcc
Applicable To
- Congenital splenomegaly
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
- 2023 (effective 10/1/2022): No change
Diagnosis Index entries containing back-references to Q89.09:
- spleen > Aberrant (congenital)
- spleen > Accessory (congenital)
- spleen > Anomaly, anomalous (congenital) (unspecified type) Q89.9
- congenital > spleen NEC D73.4
- congenital > spleen D73.89
- spleen > polycystic Q61.3
- polycystic > spleen D73.9
- spleen (congenital) > Displacement, displaced
- spleen > Distortion (s) (congenital)
- spleen > Ectopic, ectopia (congenital)
- spleen > Lobulation (congenital)
- spleen > Malformation (congenital)
- spleen > congenital Q89.1
- spleen > Polycystic (disease)
- congenital > Splenomegaly, splenomegalia (Bengal) (cryptogenic) (idiopathic) (tropical) R16.1
- spleen > Supernumerary (congenital)
- polysplenia > Syndrome
