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)
- isomerism of atrial appendages (with asplenia or polysplenia) (Q20.6)
Excludes 2
Conditions not included here, but the patient may have both
- inborn errors of metabolism (E70-E88)
Also Known As / Clinical Terms
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
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.
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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.