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L10.0 ICD-10-CM Code: Pemphigus vulgaris

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FY 2026 Apr update / Diseases of the skin and subcutaneous tissue (L00-L99) / Bullous disorders (L10-L14)

L10.0

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

Pemphigus vulgaris

An autoimmune blistering disease where the body's immune system attacks skin cells, causing painful blisters and erosions primarily in the mouth and on the skin.

Buddy the Bee presenting code insight

Buddy Insight

Pemphigus vulgaris is a severe autoimmune blistering disease with high morbidity and mortality if untreated, requiring intensive immunosuppressive therapy.

CMS-HCC V28

HCC 387

RAF 0.262

CMS-HCC V24

0

0

RAF 0

ACA/HHS

0

0

RAF 0

ESRD/PACE

0

0

RAF 0

RXHCC

HCC 314

RAF 0.0

Code Trumping

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Code Book Path

Official
L10Pemphigus
L10.0Pemphigus vulgaris

Inclusion Terms

Official

ICD-10-CM does not list inclusion terms for L10.0 in this effective period.

Excludes 2

Official

ICD-10-CM does not list Excludes 2 notes for L10.0 in this effective period.

Related Child Codes

Official
L10.1Pemphigus vegetans
L10.2Pemphigus foliaceous
L10.3Brazilian pemphigus [fogo selvagem]
L10.4Pemphigus erythematosus
L10.5Drug-induced pemphigus

Includes

Official

ICD-10-CM does not list Includes notes for L10.0 in this effective period.

Excludes 1

Official
  • pemphigus neonatorum (L01.03)

Code First

Official

ICD-10-CM does not list Code First sequencing instructions for L10.0 in this effective period.

Use Additional

Official

ICD-10-CM does not list Use Additional Code instructions for L10.0 in this effective period.

Code Also

Official

ICD-10-CM does not list Code Also instructions for L10.0 in this effective period.

Buddy Documentation Tip

HCC Buddy guidance
Clinical presentation with mucosal and cutaneous blisters
Positive Nikolsky sign documentation
Histopathologic findings showing acantholysis
Direct immunofluorescence results showing intercellular IgG deposits

MEAT Support

HCC Buddy guidance
Clinical presentation with mucosal and cutaneous blisters
Positive Nikolsky sign documentation
Histopathologic findings showing acantholysis
Direct immunofluorescence results showing intercellular IgG deposits

Audit Caution

HCC Buddy guidance
Confusing with bullous pemphigoid which has different prognosis
Using unspecified pemphigus codes when vulgaris type documented
Missing specific antibody test documentation
Confusing with other blistering diseases

Common Mistakes

HCC Buddy guidance
L12.0 — Bullous pemphigoid which has subepidermal blistering
L51.1 — Stevens-Johnson syndrome with different pathophysiology
L13.0 — Dermatitis herpetiformis with different antibody pattern
B00.2 — Herpes simplex dermatitis with viral etiology

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 L10.0 an HCC code?

Yes. L10.0 maps to Pemphigus and Other Autoimmune Skin Conditions under the CMS-HCC V28 risk adjustment model.

HCC Category Mapping

V28HCC 387, Pemphigus and Other Autoimmune Skin Conditions
0.262
RxHCCHCC 314, Pemphigus
0.000

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 L10.0

For L10.0to 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 L10.0 during that encounter, not just copy-forwarded from a problem list.

What This Code Means

L10.0 is the ICD-10-CM diagnosis code for pemphigus vulgaris. An autoimmune blistering disease where the body's immune system attacks skin cells, causing painful blisters and erosions primarily in the mouth and on the skin. L10.0 sits in the ICD-10-CM chapter for diseases of the skin and subcutaneous tissue (l00-l99), within the section covering bullous disorders (l10-l14).

Under the CMS-HCC V28 risk adjustment model, L10.0 maps to Pemphigus and Other Autoimmune Skin Conditions (HCC 387) with a community, non-dual, aged base RAF weight of 0.262. L10.0 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.

Document whether the condition is in remission or active to support medical necessity. Because L10.0 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 L10.0 sourced directly from the CMS-HCC risk adjustment model files and the CMS ICD-10-CM code set.

Coding Tips

  • Document whether the condition is in remission or active to support medical necessity
  • Link to any associated malignancy codes if paraneoplastic pemphigus is suspected

Clinical Significance

Pemphigus vulgaris is a severe autoimmune blistering disease with high morbidity and mortality if untreated, requiring intensive immunosuppressive therapy. This diagnosis indicates a life-threatening condition that significantly impacts patient prognosis and requires specialized dermatological care.

Documentation Requirements

  • Clinical presentation with mucosal and cutaneous blisters
  • Positive Nikolsky sign documentation
  • Histopathologic findings showing acantholysis
  • Direct immunofluorescence results showing intercellular IgG deposits
  • Indirect immunofluorescence or ELISA results for desmoglein antibodies
  • Assessment of disease severity and extent
  • Treatment plan including immunosuppressive therapy
  • Monitoring for treatment complications

Commonly Confused Codes

  • L12.0: Bullous pemphigoid which has subepidermal blistering
  • L51.1: Stevens-Johnson syndrome with different pathophysiology
  • L13.0: Dermatitis herpetiformis with different antibody pattern
  • B00.2: Herpes simplex dermatitis with viral etiology
  • L10.89: Other pemphigus when specific type not documented

Child Codes

Code Hierarchy

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