Diagnosis Code: Q27.9

Short Description: Congenital malformation of peripheral vascular system, unsp

Long Description: Congenital malformation of peripheral vascular system, unspecified

The code Q27.9 is VALID for claim submission

Code Classification:

• Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
  • Congenital malformations of the circulatory system (Q20-Q28)
    • Other congenital malformations of peripheral vascular system (Q27)
      • Q27.9 Congenital malformation of peripheral vascular system, unsp

Code Version: 2022 ICD-10-CM

Synonyms

• Abnormal umbilical cord
• Agenesis of artery
• Angio-osteohypertrophic syndrome
• Angioosteohypotrophic syndrome
• Arterial anomaly of umbilical cord
• Arterial malformation
• Blue rubber bleb nevus
• Capillary malformation
• Capillary malformation-arteriovenous malformation syndrome
• Capillary-venous malformation
• Capillary-venous-lymphatic malformation
• CLOVE syndrome
• Congenital abnormality of systemic artery
• Congenital abnormality of systemic vein
• Congenital abnormality of vein
• Congenital anomaly of blood vessel of left lower limb
• Congenital anomaly of blood vessel of left upper limb
• Congenital anomaly of blood vessel of limb
• Congenital anomaly of blood vessel of lower limb
• Congenital anomaly of blood vessel of right lower limb
• Congenital anomaly of blood vessel of right upper limb
• Congenital anomaly of blood vessel of upper limb
• Congenital anomaly of gastrointestinal vessel
• Congenital anomaly of peripheral blood vessel
• Congenital anomaly of umbilical artery
• Congenital dysplasia of left lobe of lung co-occurrent with congenital vascular malformation
• Congenital dysplasia of right lobe of lung co-occurrent with congenital vascular malformation
• Congenital vascular malformation
• Congenital vascular nevus
• Congenital venous malformation of skin
• Cutaneous capillary malformation
• Cutaneous vascular malformation
• Diffuse lymphatic malformation
• Dysplasia of lung
• Dysplasia of lung
• Four vessels in umbilical cord
• Hereditary vascular fragility
• Infantile hemangioma of rare localization
• Microcephaly-capillary malformation syndrome
• Mixed vascular malformation
• Peripheral venous malformation
• Posterior fossa brain malformation, haemaniogma, arterial anomaly, cardiac defect and aortic coarctation, eye abnormality synodrome and sternal anomaly syndrome
• Posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome
• Primary intraosseous venous malformation
• Short umbilical cord
• Vascular anomaly of umbilical cord
• Vascular disorder of inner ear
• Vascular malformation of inner ear
• Venous anomaly of umbilical cord
• Venous malformation
• Venous remnant
• Venous valvular anomaly
• Venous-lymphatic malformation

Diagnostic Related Group(s)

The code Q27.9 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)

• Peripheral Vascular Disorders With Mcc (299)
• Peripheral Vascular Disorders With Cc (300)
• Peripheral Vascular Disorders Without Cc/mcc (301)

References to Index of Diseases and Injuries

The code Q27.9 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Anomaly of artery or vein NOS

Crosswalk Information

Similar Codes

This page was last updated on: 10/1/2023

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