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Home/Diagnosis/ICD-10 Coding for Cavernoma

ICD-10 Coding for Cavernoma

Q06.9
D18.02
Q28.3

Complete ICD-10-CM coding and documentation guide for icd-10 coding for cavernoma includes clinical validation requirements, medical necessity guidelines, and coding policies.

Also Known as:
Cavernous Malformation
Cavernous Hemangioma
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Key Information: ICD-10 Coding for Cavernoma

Essential facts and insights about ICD-10 Coding for Cavernoma

Use ICD-10 code Q06.9 for congenital malformation of spinal cord, unspecified, ensuring proper documentation in clinical notes.

Primary ICD-10-CM Codes

Congenital malformation of spinal cord, unspecified

Billable Code
Q06.9
Billable

Diagnostic Criteria

clinical:
  • • MRI shows characteristic features of cavernoma
documentation:
  • • Diagnosis explicitly states 'congenital'

Applicable To

  • • Congenital spinal cord cavernous malformation

Important Notes

  • • Ensure congenital nature is documented.

Hemangioma of intracranial structures

Billable Code
D18.02
Billable

Diagnostic Criteria

clinical:
  • • MRI showing cavernous hemangioma
documentation:
  • • No genetic markers for familial cases

Applicable To

  • • Cavernous hemangioma of brain parenchyma

Important Notes

  • • Ensure no familial history is documented.

Other specified congenital malformations of circulatory system

Billable Code
Q28.3
Billable

Diagnostic Criteria

clinical:
  • • Genetic confirmation of CCM1, CCM2, or CCM3 mutation

Applicable To

  • • Familial cerebral cavernous malformation

Important Notes

  • • Genetic testing results must be documented.
Ancillary Codes

Additional codes that may be used with this diagnosis

G89.21

Chronic pain due to trauma

Use for chronic pain associated with spinal cavernoma.

Frequently Asked Questions

What is the ICD-10 code for a congenital spinal cavernoma?

The ICD-10 code for a congenital spinal cavernoma is Q06.9, which covers congenital malformations of the spinal cord.

How is a familial cerebral cavernoma coded?

Familial cerebral cavernomas are coded as Q28.3, provided there is genetic confirmation of a CCM mutation.

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