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 guidanceOther 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 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
MappedHCC 23
RAF 0.194
ACA/HHS
MappedHCC 28
Varies by metal level
ESRD/PACE
MappedHCC 23
RAF 0.036
RXHCC
MappedHCC 43
RAF 0.063
Code Book Path
Inclusion Terms
Official- Cross syndrome
Excludes 2
OfficialICD-10-CM does not list Excludes 2 notes for E70.328 in this effective period.
Related Child Codes
Includes
OfficialICD-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
OfficialICD-10-CM does not list Code First sequencing instructions for E70.328 in this effective period.
Use Additional
OfficialICD-10-CM does not list Use Additional Code instructions for E70.328 in this effective period.
Code Also
OfficialICD-10-CM does not list Code Also instructions for E70.328 in this effective period.
Buddy Documentation Tip
MEAT Support
Audit Caution
Common Mistakes
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
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.

