Q25.40

Billable

Congenital malformation of aorta unspecified

Congenital malformation of aorta unspecified

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

Related Codes(9)
Also Known As / Clinical Terms(39)

Clinical Terms

  • Congenital anomaly of descending thoracic aorta
  • Compression of trachea and esophagus co-occurrent and due to congenital anomaly of aortic arch
  • Persistent right aortic arch
  • Congenital anomaly of abdominal aorta
  • Congenital anomaly of descending aorta distal to aortic arch
  • Dextrotransposition of aorta
  • Right aortic arch
  • Tracheal compression
  • Tracheo-oesophageal compression syndrome
  • Compression of oesophagus
  • Aortic arch anomaly, facial dysmorphism, intellectual disability syndrome
  • Dextratransposition of aorta
  • Tracheoesophageal compression syndrome
  • Congenital anomaly of aortic arch AND/OR descending aorta
  • Disorder of ascending aorta due to conotruncal malformation
  • Compression of esophagus
  • Compression of trachea
  • Compression of trachea and oesophagus co-occurrent and due to congenital anomaly of aortic arch
  • Ascending aortopathy due to conotruncal malformation
Frequently Asked Questions
What is the ICD-10 code for congenital malformation of aorta unspecified?

The ICD-10-CM code for congenital malformation of aorta unspecified is Q25.40. The full clinical description is "Congenital malformation of aorta unspecified". Q25.40 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q25.40 mean?

ICD-10-CM code Q25.40 represents “Congenital malformation of aorta unspecified”. 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 Q25.40 a billable code?

Yes, Q25.40 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q25.40 in?

Q25.40 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What codes cannot be used with Q25.40?

Q25.40 has Excludes1 notes indicating codes that cannot be used together with it, including: hypoplasia of aorta in hypoplastic left heart syndrome (Q23.4).

What SNOMED CT codes does Q25.40 map to?

Q25.40 maps to 10 SNOMED CT concepts: 763615003, 871667007, 39392002, 1366717009, 724437007, and 5 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q25.40?

Q25.40 is linked to 1 UMLS Concept Unique Identifier: C4269136. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q25.40 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital malformation of aorta unspecified 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 Q25.40?

There is no direct ICD-11 mapping available for Q25.40 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.