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G93.43 ICD-10-CM Code: Leukoencephalopathy with calcifications and cysts

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FY 2026 Apr update / Diseases of the nervous system (G00-G99) / Other disorders of the nervous system (G89-G99)

G93.43

Billable / SpecificICD-10-CMOfficial ICD-10-CMCodebook guidance

Leukoencephalopathy with calcifications and cysts

A rare inherited brain disorder featuring abnormal white matter with calcium deposits and cyst formation.

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Buddy Insight

Leukoencephalopathy with calcifications and cysts (also known as Labrune syndrome) is a rare condition characterized by progressive white matter disease with intracranial calcifications and cyst formation.

CMS-HCC V28

HCC 200

RAF 0.262

CMS-HCC V24

0

0

RAF 0

ACA/HHS

0

0

RAF 0

ESRD/PACE

0

0

RAF 0

RXHCC

0

0

RAF 0

Code Trumping

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Code Book Path

Official
G93Other disorders of brain
G93.4Other and unspecified encephalopathy
G93.43Leukoencephalopathy with calcifications and cysts

Inclusion Terms

Official

ICD-10-CM does not list inclusion terms for G93.43 in this effective period.

Excludes 2

Official
  • alcoholic encephalopathy (G31.2)
  • encephalopathy in diseases classified elsewhere (G94)
  • hypertensive encephalopathy (I67.4)
  • toxic (metabolic) encephalopathy (G92.8)

Related Child Codes

Official
G93.40Encephalopathy, unspecified
G93.41Metabolic encephalopathy
G93.42Megalencephalic leukoencephalopathy with subcortical cysts
G93.44Adult-onset leukodystrophy with axonal spheroids
G93.45Developmental and epileptic encephalopathy

Includes

Official

ICD-10-CM does not list Includes notes for G93.43 in this effective period.

Excludes 1

Official

ICD-10-CM does not list Excludes 1 notes for G93.43 in this effective period.

Code First

Official

ICD-10-CM does not list Code First sequencing instructions for G93.43 in this effective period.

Use Additional

Official

ICD-10-CM does not list Use Additional Code instructions for G93.43 in this effective period.

Code Also

Official

ICD-10-CM does not list Code Also instructions for G93.43 in this effective period.

Buddy Documentation Tip

HCC Buddy guidance
Neuroimaging demonstrating the triad of leukoencephalopathy, calcifications, and cysts
CT scan showing intracranial calcifications and MRI showing white matter changes
Clinical documentation of progressive neurological symptoms
Genetic testing for SNORD118 mutations when available

MEAT Support

HCC Buddy guidance
Neuroimaging demonstrating the triad of leukoencephalopathy, calcifications, and cysts
CT scan showing intracranial calcifications and MRI showing white matter changes
Clinical documentation of progressive neurological symptoms
Genetic testing for SNORD118 mutations when available

Audit Caution

HCC Buddy guidance
Using nonspecific codes for intracranial calcification or white matter disease when this specific diagnosis has been established
Confusing with other leukoencephalopathies that share some imaging features but have different clinical profiles
Not documenting all three components (leukoencephalopathy, calcifications, cysts) on imaging studies
Failing to separately code seizures or other neurological manifestations

Common Mistakes

HCC Buddy guidance
G93.42 — Megalencephalic leukoencephalopathy with subcortical cysts: different pathology without calcifications, typically childhood onset with macrocephaly
G93.44 — Adult-onset leukodystrophy with axonal spheroids: lacks calcifications and cysts, different genetic basis
I67.7 — Cerebral arteritis, not elsewhere classified: may have calcifications but represents vascular inflammation
E83.52 — Hypercalcemia: metabolic cause of intracranial calcification, not a primary white matter disease

Last updated: FY2026 ICD-10-CM Apr update, Apr 1, 2026 through Sep 30, 2026. CMS-HCC V28 is 100% phased in for payment year 2026.

Is G93.43 an HCC code?

Yes. G93.43 maps to Cerebellar Ataxia and Other Degenerative Diseases of Nervous System under the CMS-HCC V28 risk adjustment model.

HCC Category Mapping

V28HCC 200, Cerebellar Ataxia and Other Degenerative Diseases of Nervous System
0.262

RAF weights shown are the community, non-dual, aged base weights from the CMS risk adjustment model file. Actual per-patient RAF contribution depends on member segment, interactions, and the model year used by the payer. V28 is the CMS-HCC model phased in over payment years 2024–2026; V24 remains in use during the transition and for historical data.

MEAT Criteria for G93.43

For G93.43to count as a valid HCC diagnosis in a given encounter, the provider's documentation must show MEAT: Monitor, Evaluate, Assess, or Treat. A diagnosis from a prior year does not carry forward automatically, it has to be re-documented and supported each calendar year.

  • MMonitor: signs, symptoms, disease progression, or lab trending documented in the note
  • EEvaluate: test results, medication response, or physical findings reviewed by the provider
  • AAssess: explicit mention in the assessment or plan with acknowledgment of status
  • TTreat: medication, referral, procedure, therapy, or counseling tied to the diagnosis

Only one of M/E/A/T is required to support the code, but the documentation must be specific enough to show that the provider actually addressed G93.43 during that encounter, not just copy-forwarded from a problem list.

What This Code Means

G93.43 is the ICD-10-CM diagnosis code for leukoencephalopathy with calcifications and cysts. A rare inherited brain disorder featuring abnormal white matter with calcium deposits and cyst formation. G93.43 sits in the ICD-10-CM chapter for diseases of the nervous system (g00-g99), within the section covering other disorders of the nervous system (g89-g99).

Under the CMS-HCC V28 risk adjustment model, G93.43 maps to Cerebellar Ataxia and Other Degenerative Diseases of Nervous System (HCC 200) with a community, non-dual, aged base RAF weight of 0.262. G93.43 was not retained as a payment HCC under the older V24 model, so V28 introduced or recategorized it during the 2024–2026 phase-in. V28 is the CMS-HCC risk adjustment model that reached 100% phase-in for payment year 2026, replacing V24 which was used during the PY2024–PY2025 transition.

Imaging findings of calcifications and cysts are essential for accurate coding of this condition. Because G93.43 maps to a payment HCC, the provider's documentation must satisfy MEAT criteria (Monitor, Evaluate, Assess, or Treat) for the encounter to count toward the patient's Medicare Advantage risk adjustment score. When documentation is ambiguous, coders should issue a provider query rather than assume the highest-specificity variant.

HCC Buddy maintains structured V28 and V24 mapping, RAF weights, and MEAT documentation criteria for G93.43 sourced directly from the CMS-HCC risk adjustment model files and the CMS ICD-10-CM code set.

Coding Tips

  • Imaging findings of calcifications and cysts are essential for accurate coding of this condition
  • This is a specific leukodystrophy; ensure differentiation from other white matter disorders

Clinical Significance

Leukoencephalopathy with calcifications and cysts (also known as Labrune syndrome) is a rare condition characterized by progressive white matter disease with intracranial calcifications and cyst formation. It can present at any age and causes progressive neurological deterioration including cognitive decline, seizures, and movement disorders. The presence of calcifications and cysts on imaging distinguishes it from other leukoencephalopathies.

Documentation Requirements

  • Neuroimaging demonstrating the triad of leukoencephalopathy, calcifications, and cysts
  • CT scan showing intracranial calcifications and MRI showing white matter changes
  • Clinical documentation of progressive neurological symptoms
  • Genetic testing for SNORD118 mutations when available
  • Current neurological examination and functional status assessment

Commonly Confused Codes

  • G93.42: Megalencephalic leukoencephalopathy with subcortical cysts: different pathology without calcifications, typically childhood onset with macrocephaly
  • G93.44: Adult-onset leukodystrophy with axonal spheroids: lacks calcifications and cysts, different genetic basis
  • I67.7: Cerebral arteritis, not elsewhere classified: may have calcifications but represents vascular inflammation
  • E83.52: Hypercalcemia: metabolic cause of intracranial calcification, not a primary white matter disease

Child Codes

Code Hierarchy

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