Q89.01 Asplenia (congenital)

The ICD-10-CM code for Asplenia (congenital) is Q89.01 (FY2026). It is a billable, claim-ready diagnosis code.

Classification

Chapter

17: Congenital malformations, deformations and chromosomal abnormalities (Q00-QA0)

Section

Q80-Q89: Other congenital malformations (Q80-Q89)

Category Q89

13 codes (10 billable)

FY2026 Status

Stable since FY2024

Also Known As

ICD-10-CM Alphabetic Index entries that lead to Q89.01:

• Ivemark's syndrome (asplenia with congenital heart disease)
• Asplenia (congenital)
• Aplasia › spleen
• Absence (of) (organ or part) (complete or partial) › spleen (congenital)
• Agenesis › spleen
• Syndrome › Ivemark's
• Anomaly, anomalous (congenital) (unspecified type) › spleen › agenesis
• Syndrome › splenic › agenesis

U.S. Hospital Utilization

• An estimated 7,515 U.S. inpatient stays in 2023 included Q89.01 among the documented diagnoses.

Source: National Inpatient Sample (NIS), Healthcare Cost and Utilization Project (HCUP), Agency for Healthcare Research and Quality, 2016–2023. National survey-weighted estimates.

Official Coding Guidelines

POA indicator for congenital conditions/anomalies and Q00-Q99 exception

Congenital conditions and anomalies Assign “Y” for congenital conditions and anomalies except for categories Q00- Q99, Congenital anomalies, which are on the exempt list. Congenital conditions are always considered present on admission.

Source: CMS — ICD-10-CM Official Guidelines for Coding and Reporting, FY2026

References

• CMS — ICD-10-CM Official Code Set and Guidelines, FY2026
• CDC/NCHS — ICD-10-CM Files and Browser Tool
• AHRQ — HCUP National Inpatient Sample, Frequencies by Diagnosis Code (2016–2023)