AutoICD API

Q27.9

Billable

Congenital malformation of peripheral vascular system, unsp

Congenital malformation of peripheral vascular system, unspecified

Coding Notes

Related Codes(6)
ICD-11 Equivalents(1)
Also Known As / Clinical Terms(214)

SNOMED CT

Clinical Terms

  • Posterior fossa brain malformation, haemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome
  • Congenital anomaly of blood vessel of left lower limb
  • Four vessels in umbilical cord
  • Capillary-venous-lymphatic malformation
  • Short umbilical cord
  • Angioosteohypertrophic syndrome
  • CLOVES syndrome
  • Congenital anomaly of blood vessels of both lower limbs
  • Intraosseous haemangioma
  • Agenesis of artery
  • Congenital anomaly of artery
  • Congenital anomaly of blood vessel of right lower extremity
  • Congenital vascular hamartoma
  • Capillary fragility - hereditary
  • Intraosseous hemangioma
  • Infantile hemangioma of rare localization
  • Combined vascular malformation
  • Congenital lipomatous overgrowth, vascular malformation, epidermal naevi, skeletal anomaly syndrome
  • Congenital vascular malformation of skin
  • Congenital venous malformation of skin
  • Congenital abnormality of systemic vein
  • Congenital lipomatous overgrowth, vascular malformation, epidermal nevi, skeletal anomaly syndrome
  • Congenital vascular nevus
  • Congenital anomaly of blood vessels of bilateral upper extremities
  • Congenital anomaly of peripheral blood vessel
  • Servelle Martorell syndrome
  • Angio-osteohypotrophic syndrome
  • Arterial malformation
  • Capillary-venous malformation
  • Blue rubber bleb nevus syndrome
  • Congenital dysplasia of right lobe of lung co-occurrent with congenital vascular malformation
  • Peripheral venous malformation
  • Venous valvular anomaly
  • Osseous venous malformation
  • Congenital anomaly of gastrointestinal vessel
  • Venous malformation
  • Capillary malformation-arteriovenous malformation syndrome
  • Congenital anomaly of blood vessel of limb
  • Congenital anomaly of blood vessel of right upper extremity
  • Congenital anomaly of blood vessel of right lower limb
  • Congenital abnormality of artery
  • Pascual Castroviejo syndrome type 2
  • Vascular malformation peripheral
  • Venous anomaly of umbilical cord
  • Congenital anomaly of capillary
  • Bilateral congenital anomaly of blood vessels of lower limbs
  • CLOVE syndrome
  • Diffuse lymphatic malformation
  • Blue rubber bleb naevus syndrome
  • Peripheral vascular congenital anomaly
  • Congenital anomaly of blood vessels of bilateral upper limbs
  • Congenital arterial malformation
  • Posterior cord syndrome due to vascular malformation
  • Anomaly of artery or vein NOS
  • Congenital anomaly of blood vessel of left upper limb
  • Diffuse capillary malformation with overgrowth
  • Congenital anomaly of blood vessel of right upper limb
  • Congenital anomaly of blood vessels of both upper limbs
  • Vascular disorder of inner ear
  • Congenital anomaly of blood vessel of left lower extremity
  • Congenital abnormality of systemic artery
  • Congenital dysplasia of left lobe of lung co-occurrent with congenital vascular malformation
  • Congenital abnormality of vein
  • Blue rubber bleb nevus
  • Arterial anomaly of umbilical cord
  • Cutaneous capillary vascular malformation
  • PHACE syndrome
  • Posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome
  • Congenital vascular anomaly
  • Congenital vascular malformation
  • Abnormal umbilical cord
  • Congenital anomaly of blood vessels of bilateral lower limbs
  • Congenital vascular naevus
  • Venous-lymphatic malformation
  • Congenital anomaly of valve of vein
  • Angio-osteohypertrophic syndrome
  • Vascular malformation of inner ear
  • Phlebectatic osteohypoplastic angiodysplasia
  • Infantile haemangioma of rare localisation
  • Vascular anomaly of umbilical cord
  • Capillary malformation
  • Primary intraosseous venous malformation
  • Vascular malformation
  • Cutaneous vascular malformation
  • Congenital anomaly of the peripheral vascular system, unspecified site
  • Congenital vascular anomaly of upper limb
  • Bilateral congenital anomaly of blood vessels of upper limbs
  • Congenital anomaly of blood vessel of left upper extremity
  • Hereditary vascular fragility
  • DCMO - diffuse capillary malformation with overgrowth
  • Infantile hemangioma
  • Congenital anomaly of blood vessel of upper limb
  • Dysplasia of lung
  • Congenital anomaly of vein
  • Infantile haemangioma
  • VM - Vascular malformation
  • Congenital anomaly of blood vessels of bilateral lower extremities
  • Cutaneous capillary malformation
  • Mixed vascular malformation
  • Venous remnant
  • Short cord
  • Congenital anomaly of blood vessel of extremity
  • Microcephaly-capillary malformation syndrome
  • Blue rubber bleb naevus
  • Congenital anomaly of blood vessel of lower limb
  • Angioosteohypotrophic syndrome
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.

How does Q27.9 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital malformation of peripheral vascular system, unsp 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 Q27.9?

Q27.9 maps to the ICD-11 code: LA90.Z (Structural developmental anomalies of the peripheral vascular system, unspecified).

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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.