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)

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

    
Non-Billable/Non-Specific Code

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