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E70.328 ICD-10-CM Code: Other oculocutaneous albinism

E70.328 is not a CMS-HCC payment code. MEAT criteria · RAF calculator · HCC Buddy coding tools

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FY 2026 Apr update / Endocrine, nutritional and metabolic diseases (E00-E89) / Metabolic disorders (E70-E88)

E70.328

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

Other oculocutaneous albinism

This code describes a rare form of albinism that affects both the skin and eyes, causing reduced pigmentation in these areas. It is a genetic condition where the body cannot properly produce or distribute melanin, the pigment responsible for skin and eye color.

Buddy the Bee presenting code insight

Buddy Insight

Other oculocutaneous albinism captures rare subtypes beyond the classic tyrosinase-negative and tyrosinase-positive forms, including Types 3 (TYRP1 mutations, more common in individuals of African descent) and Type 4 (SLC45A2 mutations).

CMS-HCC V28

N/A

Not mapped

CMS-HCC V24

HCC 23

RAF 0.194

ACA/HHS

HCC 28

Varies by metal level

ESRD/PACE

HCC 23

RAF 0.036

RXHCC

HCC 43

RAF 0.063

Code Book Path

Official
E70.3Albinism
E70.32Oculocutaneous albinism
E70.328Other oculocutaneous albinism

Inclusion Terms

Official
  • Cross syndrome

Excludes 2

Official

ICD-10-CM does not list Excludes 2 notes for E70.328 in this effective period.

Related Child Codes

Official
E70.320Tyrosinase negative oculocutaneous albinism
E70.321Tyrosinase positive oculocutaneous albinism
E70.329Oculocutaneous albinism, unspecified

Includes

Official

ICD-10-CM does not list Includes notes for E70.328 in this effective period.

Excludes 1

Official
  • Chediak-Higashi syndrome (E70.330)
  • Hermansky-Pudlak syndrome (E70.331)

Code First

Official

ICD-10-CM does not list Code First sequencing instructions for E70.328 in this effective period.

Use Additional

Official

ICD-10-CM does not list Use Additional Code instructions for E70.328 in this effective period.

Code Also

Official

ICD-10-CM does not list Code Also instructions for E70.328 in this effective period.

Buddy Documentation Tip

HCC Buddy guidance
Documentation should specify the genetic mutation or clinical subtype identified, detailed pigmentation assessment of skin, hair, and eyes, ophthalmologic examination findings, and genetic counseling records.
The provider should document why this case does not fit the tyrosinase-negative or tyrosinase-positive categories.
Family history and inheritance pattern analysis should be included.

MEAT Support

HCC Buddy guidance
Documentation should specify the genetic mutation or clinical subtype identified, detailed pigmentation assessment of skin, hair, and eyes, ophthalmologic examination findings, and genetic counseling records.
The provider should document why this case does not fit the tyrosinase-negative or tyrosinase-positive categories.
Family history and inheritance pattern analysis should be included.

Audit Caution

HCC Buddy guidance
Use this code only when the oculocutaneous albinism type has been identified but does not fit the tyrosinase-negative or tyrosinase-positive categories.
Do not use as a default when genetic testing has not been performed.
Code all ophthalmologic and dermatologic complications separately.
Document the specific genetic or clinical basis for this classification.

Common Mistakes

HCC Buddy guidance
E70.320 (Tyrosinase negative) and E70.321 (Tyrosinase positive) are for the classic subtypes.
E70.329 (Oculocutaneous albinism, unspecified) is for cases where the subtype truly cannot be determined.
E70.310-E70.319 (Ocular albinism) involves only the eyes.
E70.330-E70.339 (Albinism with hematologic abnormality) involves blood cell disorders.

Current with CMS: FY2026 ICD-10-CM Apr 1 update (effective Apr 1 – Sep 30, 2026) · CMS-HCC V28, 100% phased in for payment year 2026. FY2027 code set already staged for October 1, 2026. How HCC Buddy stays current →

Is E70.328 an HCC code?

Yes. E70.328 maps to Other Significant Endocrine and Metabolic Disorders under the V24 model but is not retained in V28.

Code
E70.328
Description
Other oculocutaneous albinism
HCC (V28)
No CMS-HCC V28 mapping
RAF
Billable
Yes
Payment year
2026

HCC Category Mapping

V24HCC 23, Other Significant Endocrine and Metabolic Disorders
0.194
ESRDHCC 23, Other Significant Endocrine and Metabolic Disorders
0.036
RxHCCHCC 43, Other Significant Endocrine and Metabolic Disorders
0.063

Each model's RAF is its CMS base weight for that model's standard population, so weights are not directly comparable across models: CMS-HCC V28 and V24 use Community, Non-Dual, Aged; ESRD uses the dialysis continuing-enrollee model; RxHCC is the Part D continuing-enrollee, non-low-income, aged weight (a larger scale than CMS-HCC). ACA/HHS has no single weight — it varies by metal level. 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.

Work E70.328 in the Code Book — tabular path, V28 RAF, and MEAT checklist →

MEAT Criteria for E70.328

For E70.328 to 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 E70.328 during that encounter, not just copy-forwarded from a problem list.

Coder workflow notes

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What This Code Means

E70.328 is the ICD-10-CM diagnosis code for other oculocutaneous albinism. This code describes a rare form of albinism that affects both the skin and eyes, causing reduced pigmentation in these areas. It is a genetic condition where the body cannot properly produce or distribute melanin, the pigment responsible for skin and eye color. E70.328 sits in the ICD-10-CM chapter for endocrine, nutritional and metabolic diseases (e00-e89), within the section covering metabolic disorders (e70-e88).

Under the older CMS-HCC V24 model, E70.328 maps to Other Significant Endocrine and Metabolic Disorders (HCC 23) with a community, non-dual, aged base RAF weight of 0.194. 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.

Verify the specific type of oculocutaneous albinism documented by the provider, as codes E70.320-E70.329 distinguish between different subtypes; E70.328 is used when the type doesn't fit other specified categories. Because E70.328 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 E70.328 sourced directly from the CMS-HCC risk adjustment model files and the CMS ICD-10-CM code set.

Coding Tips

  • Verify the specific type of oculocutaneous albinism documented by the provider, as codes E70.320-E70.329 distinguish between different subtypes; E70.328 is used when the type doesn't fit other specified categories
  • Ensure documentation clearly indicates involvement of both eyes and skin; if only one system is affected, a different albinism code may be more appropriate

Clinical Significance

Other oculocutaneous albinism captures rare subtypes beyond the classic tyrosinase-negative and tyrosinase-positive forms, including Types 3 (TYRP1 mutations, more common in individuals of African descent) and Type 4 (SLC45A2 mutations). These forms vary in severity of pigment reduction and associated visual impairment, and proper subtype identification is important for genetic counseling and management optimization.

Documentation Requirements

  • Documentation should specify the genetic mutation or clinical subtype identified, detailed pigmentation assessment of skin, hair, and eyes, ophthalmologic examination findings, and genetic counseling records.
  • The provider should document why this case does not fit the tyrosinase-negative or tyrosinase-positive categories.
  • Family history and inheritance pattern analysis should be included.

Commonly Confused Codes

  • E70.320 (Tyrosinase negative) and E70.321 (Tyrosinase positive) are for the classic subtypes.
  • E70.329 (Oculocutaneous albinism, unspecified) is for cases where the subtype truly cannot be determined.
  • E70.310-E70.319 (Ocular albinism) involves only the eyes.
  • E70.330-E70.339 (Albinism with hematologic abnormality) involves blood cell disorders.

Child Codes

Code Hierarchy

Because E70.328 maps to a payment HCC, the documentation must also satisfy MEAT criteria (Monitor, Evaluate, Assess, or Treat) for the encounter to count toward the patient's risk adjustment score.

Work E70.328 in HCC Buddy

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