E70.30 ICD-10-CM Code: Albinism, unspecified
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FY 2026 Apr update / Endocrine, nutritional and metabolic diseases (E00-E89) / Metabolic disorders (E70-E88)
E70.30
Billable / SpecificICD-10-CMOfficial ICD-10-CMCodebook guidanceAlbinism, unspecified
A genetic condition where the body produces little to no melanin (pigment), resulting in very light skin, hair, and eyes, but the specific type is not specified.

Buddy Insight
Albinism, unspecified, indicates a genetic condition with absent or significantly reduced melanin production, but the specific type (ocular, oculocutaneous, or with hematologic abnormality) has not been determined.
CMS-HCC V28
00
RAF 0
CMS-HCC V24
MappedHCC 23
RAF 0.230
ACA/HHS
00
RAF 0
ESRD/PACE
MappedHCC 23
RAF 0.0
RXHCC
MappedHCC 43
RAF 0.0
Code Trumping
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Code Book Path
Inclusion Terms
OfficialICD-10-CM does not list inclusion terms for E70.30 in this effective period.
Excludes 2
OfficialICD-10-CM does not list Excludes 2 notes for E70.30 in this effective period.
Related Child Codes
Includes
OfficialICD-10-CM does not list Includes notes for E70.30 in this effective period.
Excludes 1
OfficialICD-10-CM does not list Excludes 1 notes for E70.30 in this effective period.
Code First
OfficialICD-10-CM does not list Code First sequencing instructions for E70.30 in this effective period.
Use Additional
OfficialICD-10-CM does not list Use Additional Code instructions for E70.30 in this effective period.
Code Also
OfficialICD-10-CM does not list Code Also instructions for E70.30 in this effective period.
Buddy Documentation Tip
MEAT Support
Audit Caution
Common Mistakes
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 E70.30 an HCC code?
Yes. E70.30 maps to Other Significant Endocrine and Metabolic Disorders under the V24 model but is not retained in V28.
HCC Category Mapping
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.
Work E70.30 in the Code Book — tabular path, V28 RAF, and MEAT checklist →
MEAT Criteria for E70.30
For E70.30to 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 E70.30 during that encounter, not just copy-forwarded from a problem list.
Coder workflow notes
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What This Code Means
E70.30 is the ICD-10-CM diagnosis code for albinism, unspecified. A genetic condition where the body produces little to no melanin (pigment), resulting in very light skin, hair, and eyes, but the specific type is not specified. E70.30 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, E70.30 maps to Other Significant Endocrine and Metabolic Disorders (HCC 23) with a community, non-dual, aged base RAF weight of 0.230. 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.
Albinism has multiple subtypes; review clinical documentation to determine if ocular or oculocutaneous albinism is present. Because E70.30 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 E70.30 sourced directly from the CMS-HCC risk adjustment model files and the CMS ICD-10-CM code set.
Coding Tips
- •Albinism has multiple subtypes; review clinical documentation to determine if ocular or oculocutaneous albinism is present
- •Document any associated vision problems or skin complications for complete coding
Clinical Significance
Albinism, unspecified, indicates a genetic condition with absent or significantly reduced melanin production, but the specific type (ocular, oculocutaneous, or with hematologic abnormality) has not been determined. Patients face increased risks of skin cancer from ultraviolet exposure, significant visual impairment including nystagmus and photophobia, and social stigmatization, requiring multidisciplinary management including dermatologic surveillance and ophthalmologic care.
Documentation Requirements
- ✓Documentation should describe the extent of pigment loss (skin only, eyes only, or both), visual acuity findings, nystagmus assessment, and skin examination results.
- ✓The provider should specify whether this is ocular or oculocutaneous albinism and document any hematologic abnormalities.
- ✓Genetic testing results and family history should be included.
- ✓Skin cancer screening frequency and sun protection counseling should be noted.
Commonly Confused Codes
- •E70.310-E70.319 (Ocular albinism codes) specify eye-only involvement.
- •E70.320-E70.329 (Oculocutaneous albinism codes) specify skin and eye involvement.
- •E70.330-E70.339 (Albinism with hematologic abnormality) includes bleeding or immune disorders.
- •E70.39 (Other specified albinism) covers other variants.
- •L80 (Vitiligo) involves acquired rather than congenital pigment loss.