Q89.0
Non-billableCongenital absence and malformations of spleen
Congenital absence and malformations of spleen
This is a header/category code. For billing purposes, use a more specific child code from the list below.
Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
Child Codes (2)
Related Codes(7)
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
Q89.9Congenital malformation, unspecified
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(1)
Frequently Asked Questions
What is the ICD-10 code for congenital absence and malformations of spleen?
The ICD-10-CM code for congenital absence and malformations of spleen is Q89.0. The full clinical description is "Congenital absence and malformations of spleen". Q89.0 is a non-billable header code. Use a more specific child code for billing purposes.
What does ICD-10 code Q89.0 mean?
ICD-10-CM code Q89.0 represents “Congenital absence and malformations of spleen”. It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a non-billable header code. Use a more specific child code for billing purposes.
Is Q89.0 a billable code?
No, Q89.0 is a non-billable header code. You need to use one of its more specific child codes for billing. There are 2 child codes under Q89.0.
What chapter is Q89.0 in?
Q89.0 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q89.0?
Q89.0 has Excludes1 notes indicating codes that cannot be used together with it, including: isomerism of atrial appendages (with asplenia or polysplenia) (Q20.6).
What are the subcategories under Q89.0?
Q89.0 has 2 child codes, including: Q89.01 (Asplenia (congenital)), Q89.09 (Congenital malformations of spleen).
What are the UMLS CUIs for Q89.0?
Q89.0 is linked to 1 UMLS Concept Unique Identifier: C2910349. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q89.0 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital absence and malformations of spleen affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of Q89.0?
Q89.0 maps to the ICD-11 code: LB22.Z (Structural developmental anomalies of spleen, unspecified).
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.