ICD-10-CM · Chapter 17 · Q00–Q99
Q89.01
Asplenia (congenital)
Congenital malformations, deformations and chromosomal abnormalities
Quick facts
- Code
- Q89.01
- Type
- Billable code
- ICD-10-CM chapter
- Chapter 17 — Congenital malformations, deformations and chromosomal abnormalities
- Category
- Q89 — Other congenital malformations, not elsewhere classified
- Specificity
- 5 characters
How coders use this code
ICD-10-CM Q89.01 is a billable, fully specified code, so it can be reported directly on a claim to document a diagnosis of asplenia (congenital). Coders assign it when the chart documentation supports this level of detail, always matching to the most specific code available and verifying against the chapter-specific guidelines published annually by NCHS/CMS.
Related codes in Q89
- Q89Other congenital malformations, not elsewhere classified
- Q89.0Congenital absence and malformations of spleen
- Q89.09Congenital malformations of spleen
- Q89.1Congenital malformations of adrenal gland
- Q89.2Congenital malformations of other endocrine glands
- Q89.3Situs inversus
- Q89.4Conjoined twins
- Q89.7Multiple congenital malformations, not elsewhere classified
- Q89.8Other specified congenital malformations
- Q89.81Kabuki syndrome
- Q89.89Other specified congenital malformations
- Q89.9Congenital malformation, unspecified
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