Q27.30
BillableArteriovenous malformation, site unspecified
Arteriovenous malformation, site unspecified
Status
Billable / Specific
Parent Code
Q27.3Coding 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
- •inborn errors of metabolismE70-E88
- •anomalies of cerebral and precerebral vesselsQ28.0-Q28.3
- •anomalies of coronary vesselsQ24.5
- •anomalies of pulmonary arteryQ25.5-Q25.7
- •congenital retinal aneurysmQ14.1
- •hemangioma and lymphangiomaD18
- •arteriovenous malformation of cerebral vesselsQ28.2
- •arteriovenous malformation of precerebral vesselsQ28.0
Related Codes(5)
Q27.31Arteriovenous malformation of vessel of upper limb
Q27.32Arteriovenous malformation of vessel of lower limb
Q27.33Arteriovenous malformation of digestive system vessel
Q27.34Arteriovenous malformation of renal vessel
Q27.39Arteriovenous malformation, other site
Also Known As / Clinical Terms(83)
SNOMED CT
- AV - Congenital arteriovenous anomaly234141001
- AV - Congenital arteriovenous malformation234141001
- AVM - Congenital arteriovenous malformation234141001
- Congenital arteriovenous malformation234141001
- Congenital AV - arteriovenous fistula234148007
- Congenital arteriovenous fistula234148007
- Congenital arteriovenous fistula - disorder234148007
- Congenital arteriovenous fistula occlusion234150004
- Congenital arteriovenous fistula stenosis234151000
- Congenital arteriovenous fistula thrombosis234152007
- Congenital arteriovenous fistula infection234153002
- Congenital arteriovenous fistula aneurysm234154008
- Congenital arteriovenous fistula rupture234156005
- Arteriovenous fistula occlusion234202005
- Arteriovenous fistula stenosis234203000
- Arteriovenous fistula clotted234205007
- Arteriovenous fistula thrombosis234205007
- Arteriovenous fistula infection234206008
- Arteriovenous fistula rupture234208009
- Vascular malformation of the nervous system253193002
- Cobb syndrome254774003
- Cobb's syndrome254774003
- Peripheral arteriovenous malformation275519006
- Arteriovenous fistula aneurysm302946006
- Hereditary disorder of lymphatic system363190001
- Autosomal dominant familial haematuria, retinal arteriolar tortuosity, contractures702428000
- Autosomal dominant familial hematuria, retinal arteriolar tortuosity, contractures702428000
- HANAC - hereditary angiopathy with nephropathy, aneurysms, and muscle cramps702428000
- HANAC syndrome702428000
- Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome702428000
- Peripheral venous malformation703198009
- Arteriovenous malformation of limb703331008
- Capillary malformation-arteriovenous malformation syndrome703533007
- PTEN hamartoma tumor syndrome722859001
- PTEN hamartoma tumour syndrome722859001
- SOLAMEN syndrome763867001
- Segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal naevus syndrome763867001
- Segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus syndrome763867001
- Congenital systemic arteriovenous fistula786041005
- Congenital anomaly of blood vessel of spine1155723008
- Congenital anomaly of spinal blood vessel1155723008
Clinical Terms
- Congenital arteriovenous fistula thrombosis
- Arteriovenous fistula clotted
- Congenital arteriovenous fistula rupture
- Congenital systemic arteriovenous fistula
- Congenital arteriovenous fistula stenosis
- HANAC - hereditary angiopathy with nephropathy, aneurysms, and muscle cramps
- PTEN hamartoma tumour syndrome
- Autosomal dominant familial haematuria, retinal arteriolar tortuosity, contractures
- AVM - Congenital arteriovenous malformation
- AV - Congenital arteriovenous anomaly
- Peripheral arteriovenous malformation
- Cobb's syndrome
- Arteriovenous fistula occlusion
- Arteriovenous fistula rupture
- Cobb syndrome
- Arteriovenous fistula thrombosis
- Segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus syndrome
- Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome
- Congenital arteriovenous fistula
- Arteriovenous fistula stenosis
- SOLAMEN syndrome
- Congenital arteriovenous fistula aneurysm
- Congenital anomaly of spinal blood vessel
- Arteriovenous malformation of limb
- Vascular malformation of the nervous system
- Hereditary disorder of lymphatic system
- Segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal naevus syndrome
- Congenital arteriovenous fistula occlusion
- HANAC syndrome
- Arteriovenous fistula aneurysm
- Autosomal dominant familial hematuria, retinal arteriolar tortuosity, contractures
- Congenital anomaly of blood vessel of spine
- Congenital arteriovenous fistula - disorder
- Arteriovenous fistula infection
- Congenital AV - arteriovenous fistula
- AV - Congenital arteriovenous malformation
- Peripheral venous malformation
- Congenital arteriovenous fistula infection
- Congenital arteriovenous malformation
- PTEN hamartoma tumor syndrome
- Capillary malformation-arteriovenous malformation syndrome
Frequently Asked Questions
What is the ICD-10 code for arteriovenous malformation, site unspecified?
The ICD-10-CM code for arteriovenous malformation, site unspecified is Q27.30. The full clinical description is "Arteriovenous malformation, site unspecified". Q27.30 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q27.30 mean?
ICD-10-CM code Q27.30 represents “Arteriovenous malformation, site 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 Q27.30 a billable code?
Yes, Q27.30 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q27.30 in?
Q27.30 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q27.30?
Q27.30 has Excludes1 notes indicating codes that cannot be used together with it, including: acquired arteriovenous aneurysm (I77.0).
What SNOMED CT codes does Q27.30 map to?
Q27.30 maps to 26 SNOMED CT concepts: 234141001, 302946006, 234205007, 234206008, 234202005, and 21 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q27.30?
Q27.30 is linked to 1 UMLS Concept Unique Identifier: C2910144. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q27.30 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like arteriovenous malformation, site 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 Q27.30?
There is no direct ICD-11 mapping available for Q27.30 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.