Q89.0 - Congenital absence and malformations of spleen
- Applicable to Congenital absence and malformations of spleen
- The 2025 edition of ICD10-CM Q89.0 became effective on October 1, 2024.
- This is the American ICD10-CM version of Q89.0 - other international versions of ICD10 Q89.0 may differ.
- Q89.0 is a Non-Billable / Non-Specific ICD10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- Q89.0 Code should not be used for billing or reimbursement purposes as there are multiple ICD-10 CM codes below it that contain a greater level of detail.
- Q89.0 - Congenital absence and malformations of spleen
- Q89.0 - Congenital absence and malformations of spleen
- Q89.01 - Asplenia (congenital)
- Q89.09 - Congenital malformations of spleen
Type 1 Excludes
- isomerism of atrial appendages (with asplenia or polysplenia) (Q20.6)
Non-Billable/Non-Specific Code
The following codes above Q89.0 contain annotation back-references that may be applicable to Q89.0:
- Chapter: Q00-Q99 - Congenital malformations, deformations and chromosomal abnormalities
- Section: Q80-Q89 - Other congenital malformations
- Category: Q89 - Other congenital malformations, not elsewhere classified
Browse other similar CM codes:
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
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