Q27.9
BillableCongenital malformation of peripheral vascular system, unsp
Congenital malformation of peripheral vascular system, unspecified
Status
Billable / Specific
Parent Code
Q27Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Anomaly of artery or vein NOS
Excludes 2
Conditions not included here, but the patient may have both
- inborn errors of metabolism (E70-E88)
- anomalies of cerebral and precerebral vessels (Q28.0-Q28.3)
- anomalies of coronary vessels (Q24.5)
- anomalies of pulmonary artery (Q25.5-Q25.7)
- congenital retinal aneurysm (Q14.1)
- hemangioma and lymphangioma (D18.-)
Also Known As / Clinical Terms
SNOMED CT
- Venous anomaly of umbilical cord29057008
- Vascular anomaly of umbilical cord31481000
- Arterial anomaly of umbilical cord62023000
- Abnormal umbilical cord90009001
- Short cord156222001
- Short umbilical cord156222001
- Capillary fragility - hereditary191329002
- Hereditary vascular fragility191329002
- Capillary malformation234118009
- Congenital anomaly of capillary234118009
- Arterial malformation234119001
- Congenital abnormality of artery234119001
- Congenital anomaly of artery234119001
- Congenital arterial malformation234119001
- Venous malformation234124003
- Congenital anomaly of valve of vein234125002
- Venous valvular anomaly234125002
- Capillary-venous malformation234133001
- Venous-lymphatic malformation234134007
- Capillary-venous-lymphatic malformation234136009
- Dysplasia of lung253745002
- Congenital vascular hamartoma254206003
- Congenital vascular naevus254206003
- Congenital vascular nevus254206003
- Blue rubber bleb naevus254784002
- Blue rubber bleb naevus syndrome254784002
- Blue rubber bleb nevus254784002
- Blue rubber bleb nevus syndrome254784002
- Vascular disorder of inner ear277493007
- Vascular malformation of inner ear277495000
- Venous remnant280143008
- Congenital abnormality of vein297222002
- Congenital anomaly of vein297222002
- Combined vascular malformation400017009
- Mixed vascular malformation400017009
- Congenital vascular malformation of skin400042000
- Cutaneous vascular malformation400042000
- Congenital vascular anomaly400159008
- Congenital vascular malformation400159008
- VM - Vascular malformation400159008
- Vascular malformation400159008
- Four vessels in umbilical cord417426005
- Congenital anomaly of peripheral blood vessel430166008
- Peripheral vascular congenital anomaly430166008
- Congenital anomaly of blood vessel of upper limb432293006
- Congenital vascular anomaly of upper limb432293006
- Congenital abnormality of systemic vein448065006
- Congenital anomaly of blood vessel of extremity449870006
- Congenital anomaly of blood vessel of limb449870006
- Congenital anomaly of blood vessel of lower limb449871005
- Congenital abnormality of systemic artery461440001
- PHACE syndrome698765007
- Pascual Castroviejo syndrome type 2698765007
- Posterior fossa brain malformation, haemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome698765007
- Posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome698765007
- Peripheral venous malformation703198009
- Infantile haemangioma of rare localisation703270004
- Infantile hemangioma of rare localization703270004
- Diffuse lymphatic malformation703298001
- Cutaneous capillary malformation703299009
- Cutaneous capillary vascular malformation703299009
- Microcephaly-capillary malformation syndrome703369003
- Capillary malformation-arteriovenous malformation syndrome703533007
- CLOVE syndrome719475006
- CLOVES syndrome719475006
- Congenital lipomatous overgrowth, vascular malformation, epidermal naevi, skeletal anomaly syndrome719475006
- Congenital lipomatous overgrowth, vascular malformation, epidermal nevi, skeletal anomaly syndrome719475006
- Angio-osteohypertrophic syndrome723991007
- Angioosteohypertrophic syndrome723991007
- Congenital venous malformation of skin724842007
- Intraosseous haemangioma764100007
- Intraosseous hemangioma764100007
- Osseous venous malformation764100007
- Primary intraosseous venous malformation764100007
- Angio-osteohypotrophic syndrome765750001
- Angioosteohypotrophic syndrome765750001
- Phlebectatic osteohypoplastic angiodysplasia765750001
- Servelle Martorell syndrome765750001
- Congenital dysplasia of left lobe of lung co-occurrent with congenital vascular malformation767029004
- Congenital dysplasia of right lobe of lung co-occurrent with congenital vascular malformation767030009
- Agenesis of artery789097007
- DCMO - diffuse capillary malformation with overgrowth1293116008
- Diffuse capillary malformation with overgrowth1293116008
- Infantile haemangioma1293125002
- Infantile hemangioma1293125002
- Posterior cord syndrome due to vascular malformation1343512002
- Bilateral congenital anomaly of blood vessels of lower limbs15973261000119108
- Congenital anomaly of blood vessels of bilateral lower extremities15973261000119108
- Congenital anomaly of blood vessels of bilateral lower limbs15973261000119108
- Congenital anomaly of blood vessels of both lower limbs15973261000119108
- Bilateral congenital anomaly of blood vessels of upper limbs16007671000119109
- Congenital anomaly of blood vessels of bilateral upper extremities16007671000119109
- Congenital anomaly of blood vessels of bilateral upper limbs16007671000119109
- Congenital anomaly of blood vessels of both upper limbs16007671000119109
- Congenital anomaly of blood vessel of left lower extremity15973181000119106
- Congenital anomaly of blood vessel of left lower limb15973181000119106
- Congenital anomaly of blood vessel of left upper extremity16007591000119106
- Congenital anomaly of blood vessel of left upper limb16007591000119106
- Congenital anomaly of blood vessel of right lower extremity15973221000119103
- Congenital anomaly of blood vessel of right lower limb15973221000119103
- Congenital anomaly of blood vessel of right upper extremity16007631000119106
- Congenital anomaly of blood vessel of right upper limb16007631000119106
- Congenital anomaly of gastrointestinal vessel32201000119107
UMLS
Frequently Asked Questions
What is the ICD-10 code for congenital malformation of peripheral vascular system, unsp?
The ICD-10-CM code for congenital malformation of peripheral vascular system, unsp is Q27.9. The full clinical description is "Congenital malformation of peripheral vascular system, unspecified". Q27.9 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q27.9 mean?
ICD-10-CM code Q27.9 represents "Congenital malformation of peripheral vascular system, 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 Q27.9 a billable code?
Yes, Q27.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q27.9 in?
Q27.9 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q27.9 map to?
Q27.9 maps to 55 SNOMED CT concepts: 90009001, 789097007, 723991007, 765750001, 62023000, and 50 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q27.9?
Q27.9 is linked to 2 UMLS Concept Unique Identifiers: C2910152, C0340797. 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.