2027 ICD-10-CM Diagnosis Code E76.01Hurler's syndrome

ICD-10-CM Codes›E00–E89›E70-E88›E76

ICD-10-CM E76.01
CMSSource: CMS FY 2027 ICD-10-CM dataset · Effective Oct 1, 2026 – Sep 30, 2027

E76.01 is a billable ICD-10-CM diagnosis code for Hurler's syndrome. It is valid on HIPAA claims for fiscal year 2027 (October 1, 2026 through September 30, 2027) and groups to MS-DRG 642. As a secondary diagnosis, it counts as a complication or comorbidity (CC) and moves an inpatient stay to a higher severity level within its MS-DRG family. It does not count, however, when the principal diagnosis is one of 37 closely related codes. Coders also document this condition as dysostosis multiplex. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Other specified and unspecified nutritional and metabolic disorders.

For Medicare Advantage risk adjustment, E76.01 maps to CMS-HCC Category 49 (Specified Lysosomal Storage Disorders) under the V28 model, adding a risk factor of about 9.256 for a community, non-dual, aged beneficiary in payment year 2027.

Code Identity

ICD-10-CM Code
E76.01
Billable Status
Yes — Valid for Submission
Code Describes
Hurler's syndrome
Short Description
Hurler's syndrome
Same as the full description in the CMS dataset.
Parent Code
Mucopolysaccharidosis, type I

Code Classification

ChapterE00–E89Endocrine, nutritional and metabolic diseases
SectionE70-E88Metabolic disorders
CategoryE76Disorders of glycosaminoglycan metabolism
This CodeE76.01Hurler's syndrome

Medicare Risk Adjustment (HCC)Billing

E76.01 maps to a payment category in the CMS-HCC model used to risk-adjust Medicare Advantage payments. Weights are the published community factors for payment year 2027.

CMS-HCC V28 Category (Payment Model)
HCC 49— Specified Lysosomal Storage Disorders
Payment HCC · PY 2027 one of 13 ICD-10-CM codes in this category
Risk Adjustment Factor (RAF) Weight
+9.256
community, non-dual, aged · ranges 1.528–13.778 across segments
Hierarchy
Top of its hierarchy
HCC 49 is not superseded by any other condition category
Prior Model (CMS-HCC V24)
HCC 23
V24 retired V28 pays 100% of MA risk scores since PY 2026
Other CMS Models
PACE (CMS-HCC V22): HCC 23 · ESRD (V21): HCC 23 · ESRD (V24): HCC 23
ESRD V21 weights: 0.013 dialysis, 0.234–0.359 functioning graft · ESRD V24 weights: 0.036 dialysis, 0.217–0.390 functioning graft
Part D (RxHCC)
RxHCC 41 — Lysosomal Storage Disorders
also risk-adjusts in the Part D prescription drug model (V08)

Source: CMS Payment Year 2027 risk adjustment mappings and model software. Weights are relative factors, not dollar amounts; a beneficiary's total RAF also includes demographics and interactions. Browse all CMS-HCC categories.

Approximate SynonymsGuidance

Alternate terms and clinical phrases that map to this code.

  • Dysostosis multiplex
  • Dysostosis multiplex group
  • Hurloid facies
  • Mucopolysaccharidosis, MPS-I
  • Mucopolysaccharidosis, MPS-I-H

Instructional NotesGuidance

Instructions from the official ICD-10-CM Tabular List that apply to E76.01: its own notes plus those printed at block E70-E88 and Chapter 4. A note printed at a category, block or chapter applies to every code under it.

Excludes1

Not coded here: the excluded code is never reported together with this one, unless the two conditions are unrelated.

From Block E70-E88 Metabolic disorders applies to 286 codes
  • androgen insensitivity syndrome (E34.5-)
  • congenital adrenal hyperplasia (E25.0)
  • hemolytic anemias attributable to enzyme disorders (D55.-)
  • Marfan syndrome (Q87.4-)
  • 5-alpha-reductase deficiency (E29.1)
From Chapter 4 (E00-E89) Endocrine, nutritional and metabolic diseases applies to 973 codes
  • transitory endocrine and metabolic disorders specific to newborn (P70-P74)

Excludes2

Not included here: the excluded condition is not part of this code, but a patient may have both, so both codes may be reported.

From Block E70-E88 Metabolic disorders applies to 286 codes
  • Ehlers-Danlos syndromes (Q79.6-)

Notes

General instructions on how these codes are used.

From Chapter 4 (E00-E89) Endocrine, nutritional and metabolic diseases applies to 973 codes
  • All neoplasms, whether functionally active or not, are classified in Chapter 2. Appropriate codes in this chapter (i.e. E05.8, E07.0, E16-E31, E34.-) may be used as additional codes to indicate either functional activity by neoplasms and ectopic endocrine tissue or hyperfunction and hypofunction of endocrine glands associated with neoplasms and other conditions classified elsewhere.

Source: CMS ICD-10-CM Tabular List. How to read instructional notes.

Referenced in Other NotesGuidance

Instructional notes printed at other codes that name E76.01, its category, or a range that includes it.

Excludes1 2

These codes carry an Excludes1 note naming E76.01: they are not reported together with it, unless the two conditions are unrelated.

  • E74 Other disorders of carbohydrate metabolism
    mucopolysaccharidosis (E76.0-E76.3) names E76.0-E76.3, which includes this code
  • Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine
    mucopolysaccharidosis (E76.0-E76.3) names E76.0-E76.3, which includes this code

Index to Diseases and InjuriesGuidance

Alphabetical index entries that point to this code.

Clinical ClassificationClinical

AHRQ’s CCSR groups this code into broader clinical categories.

CCSR END016
Other specified and unspecified nutritional and metabolic disorders
Default principal diagnosis: inpatient Yes · outpatient Yes

Clinical InformationClinical

  • Mucopolysaccharidosis I

    a group of autosomal recessive lysosomal storage disorders caused by mutations in the gene encoding the enzyme, alpha-l-iduronidase (idua), required for the degradation of heparan and dermatan sulfates. this leads to abnormal accumulation of these glycosaminoglycans in various tissues causing a wide range of clinical presentations including cognitive and musculoskeletal disorders.

Patient EducationClinical

Carbohydrate Metabolism Disorders

Metabolism is the process your body uses to make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Chemicals in your digestive system (enzymes) break the food parts down into sugars and acids, your body's fuel. Your body can use this fuel right away, or it can store the energy in your body tissues.

Read the full article at MedlinePlus

Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.

Convert E76.01 to ICD-9-CMHistory

The closest ICD-9-CM equivalents under the General Equivalence Mappings.

ICD-9-CM
277.5 Mucopolysaccharidosis
Approximate The match is approximate rather than exact.

Code HistoryHistory

FY 2016AddedAdded to the ICD-10-CM code setEffective October 1, 2015, the first year of ICD-10-CM.
FY 2017–2026No changes
FY 2027CurrentCurrent code set, no changesEffective October 1, 2026 through September 30, 2027.

Questions About E76.01Overview

What is the ICD-10 code for Hurler's syndrome?

The ICD-10-CM code for Hurler's syndrome is E76.01 (sometimes written as E7601). It is billable on HIPAA-covered claims from October 1, 2026 through September 30, 2027.

Is E76.01 (Mucopolysaccharidosis, type I) a billable code?

Yes. This is a billable ICD-10-CM code, specific enough to report Hurler's syndrome on HIPAA-covered claims from October 1, 2026 through September 30, 2027.

What MS-DRG does E76.01 group to?

When Hurler's syndrome is the principal diagnosis on an inpatient stay, it groups to MS-DRG 642 (inborn and Other Disorders of Metabolism), which carries a relative weight of 1.3226. Higher weights mean higher Medicare reimbursement.

Is E76.01 a CC or MCC?

CMS lists E76.01 as a CC (complication or comorbidity) for FY 2027. Reported as a secondary diagnosis, it moves the inpatient stay to a higher-weighted DRG within its severity family. It does not count when the principal diagnosis is one of the 37 closely related codes in its exclusion list.

Can E76.01 be reported with a code from E34.5?

Not as a rule. The Excludes1 note at block E70-E88, which applies to E76.01, lists "androgen insensitivity syndrome (E34.5-)". An Excludes1 note means the excluded code is never reported together with this one; the only exception is when the two conditions are unrelated to each other (Official Guidelines, Section I.A.12.a).

What HCC is E76.01?

E76.01 (Hurler's syndrome) maps to CMS-HCC Category 49 (Specified Lysosomal Storage Disorders), commonly written as HCC 49, in the CMS-HCC V28 model used for Medicare Advantage risk adjustment in payment year 2027. It mapped to HCC 23 under the retired V24 model. It also maps in the PACE (CMS-HCC V22), ESRD (V21), and ESRD (V24) models. In the Part D prescription drug model it maps to RxHCC 41.

Does E76.01 risk-adjust for Medicare Advantage payment?

Yes. When documented and reported on a Medicare Advantage encounter, E76.01 adds a risk adjustment factor of about 9.256 to the beneficiary's RAF score for a community, non-dual, aged enrollee (published V28 weights range from 1.528 to 13.778 depending on the payment segment). HCC 49 sits at the top of its hierarchy, so no other condition category supersedes it. See the full factor table on the HCC 49 category page.