Q89.09
BillableCongenital malformations of spleen
Congenital malformations of spleen
Status
Billable / Specific
Parent Code
Q89.0Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Congenital splenomegaly
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
Related Codes(1)
Also Known As / Clinical Terms(120)
SNOMED CT
- Accessory spleen10362008
- Polysplenia10362008
- Splenunculi10362008
- Supernumerary spleen10362008
- Heterotaxia14821001
- Heterotaxis14821001
- Heterotaxy14821001
- Situs ambiguus14821001
- Ectopic splenic tissue23914009
- Isomerism sequence24614000
- Laterality sequence24614000
- Congenital splenomegaly36752001
- Splenosis38831007
- Congenital lobulation of spleen42780004
- Lobulation of spleen42780004
- Anomalies of spleen57497006
- Congenital abnormality of spleen57497006
- Congenital anomaly of spleen57497006
- Congenital malformation of spleen57497006
- Splenogonadal fusion62042001
- Aberrant spleen65146007
- Ectopic spleen65146007
- Bilateral left-sidedness sequence72425000
- Polysplenia syndrome72425000
- Atresia of bile ducts77480004
- BA - Biliary atresia77480004
- Biliary atresia77480004
- Congenital biliary atresia77480004
- Cyst of spleen79040006
- Spleen cyst79040006
- Splenic cyst79040006
- Congenital abnormal shape of spleen92946005
- Congenital misshapen spleen92946005
- Congenital cyst of spleen93049005
- Serous cyst of spleen93049005
- Simple cyst of spleen93049005
- Congenital hypoplasia of spleen93292008
- Congenital microsplenia93292008
- Congenital small spleen93292008
- Congenital malposition of spleen93351001
- Congenital malpositioned spleen93351001
- Hypoplasia of spleen205735005
- Mis-shapen spleen205736006
- Polycystic spleen234504005
- Hereditary splenic hypoplasia302961007
- Spleen in right sided position448602005
- BASM syndrome717156002
- Biliary atresia with splenic malformation syndrome717156002
- SGFLD (splenogonadal fusion limb defect syndrome) syndrome726724005
- Splenogonadal fusion limb defect syndrome726724005
- Splenogonadal fusion, limb defect, micrognathia syndrome726724005
- Polysplenia heterotaxy syndrome8641000119101
UMLS
- Anomalies of spleenC0700587
- Congenital abnormality of spleenC0700587
- Congenital anomalies of spleenC0700587
- Congenital anomaly of spleenC0700587
- Congenital anomaly of spleen (disorder)C0700587
- Congenital malformation of spleenC0700587
- Congenital malformations of spleenC0700587
- Congenital spleen anomaly NOSC0700587
- Spleen malformationC0700587
- Congenital splenomegalyC0266634
- Congenital splenomegaly (disorder)C0266634
Clinical Terms
- Polycystic spleen
- Congenital splenomegaly (disorder)
- Ectopic splenic tissue
- Situs ambiguus
- Isomerism sequence
- Congenital malpositioned spleen
- Splenic cyst
- Anomalies of spleen
- Congenital misshapen spleen
- SGFLD (splenogonadal fusion limb defect syndrome) syndrome
- Heterotaxy
- Splenogonadal fusion
- Congenital biliary atresia
- BA - Biliary atresia
- Congenital malformation of spleen
- BASM syndrome
- Spleen in right sided position
- Hypoplasia of spleen
- Congenital splenomegaly
- Congenital anomaly of spleen (disorder)
- Aberrant spleen
- Splenosis
- Atresia of bile ducts
- Congenital lobulation of spleen
- Accessory spleen
- Cyst of spleen
- Heterotaxis
- Polysplenia
- Simple cyst of spleen
- Splenogonadal fusion limb defect syndrome
- Biliary atresia with splenic malformation syndrome
- Splenunculi
- Congenital microsplenia
- Heterotaxia
- Congenital abnormal shape of spleen
- Biliary atresia
- Hereditary splenic hypoplasia
- Laterality sequence
- Congenital anomalies of spleen
- Spleen malformation
- Congenital malposition of spleen
- Congenital anomaly of spleen
- Ectopic spleen
- Congenital cyst of spleen
- Congenital abnormality of spleen
- Mis-shapen spleen
- Polysplenia heterotaxy syndrome
- Polysplenia syndrome
- Serous cyst of spleen
- Spleen cyst
- Lobulation of spleen
- Bilateral left-sidedness sequence
- Congenital spleen anomaly NOS
- Splenogonadal fusion, limb defect, micrognathia syndrome
- Congenital small spleen
- Congenital hypoplasia of spleen
- Supernumerary spleen
Frequently Asked Questions
What is the ICD-10 code for congenital malformations of spleen?
The ICD-10-CM code for congenital malformations of spleen is Q89.09. The full clinical description is "Congenital malformations of spleen". Q89.09 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q89.09 mean?
ICD-10-CM code Q89.09 represents “Congenital malformations of spleen”. It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.
Is Q89.09 a billable code?
Yes, Q89.09 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q89.09 in?
Q89.09 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q89.09?
Q89.09 has Excludes1 notes indicating codes that cannot be used together with it, including: isomerism of atrial appendages (with asplenia or polysplenia) (Q20.6).
What SNOMED CT codes does Q89.09 map to?
Q89.09 maps to 25 SNOMED CT concepts: 65146007, 10362008, 57497006, 77480004, 717156002, and 20 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q89.09?
Q89.09 is linked to 2 UMLS Concept Unique Identifiers: C0700587, C0266634. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q89.09 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital 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 Q89.09?
There is no direct ICD-11 mapping available for Q89.09 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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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.