2026 ICD-10-CM Diagnosis Code H18.549Lattice corneal dystrophy, unspecified eye

ICD-10-CM Codes›H00–H59›H15-H22›H18

ICD-10-CM H18.549
CMSSource: CMS FY 2026 ICD-10-CM dataset · Effective Oct 1, 2025 – Sep 30, 2026

H18.549 is a billable ICD-10-CM diagnosis code for lattice corneal dystrophy, unspecified eye. It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026) and groups to MS-DRG 124 through 125. Coders also document this condition as amyloid of cornea. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Cornea and external disease.

Code Identity

ICD-10-CM Code
H18.549
Billable Status
Yes — Valid for Submission
Code Describes
Lattice corneal dystrophy, unspecified eye
Short Description
Lattice corneal dystrophy, unspecified eye
Same as the full description in the CMS dataset.
Parent Code
H18.54
Lattice corneal dystrophy

Code Classification

ChapterH00–H59Diseases of the eye and adnexa
SectionH15-H22Disorders of sclera, cornea, iris and ciliary body
CategoryH18Other disorders of cornea
This CodeH18.549Lattice corneal dystrophy, unspecified eye

Approximate SynonymsGuidance

Alternate terms and clinical phrases that map to this code.

  • Amyloid of cornea
  • Congenital corneal dystrophy
  • Congenital macular corneal dystrophy
  • Lattice corneal dystrophy
  • Lattice corneal dystrophy Type I
  • Lattice corneal dystrophy, isolated form
  • Localized hereditary amyloidosis
  • Macular corneal dystrophy

Clinical ClassificationClinical

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

CCSR EYE001
Cornea and external disease
Default principal diagnosis: inpatient Yes · outpatient Yes

Clinical InformationClinical

  • Macular Corneal Dystrophy

    a stromal corneal dystrophy, with autosomal recessive inheritance, that is caused by lack of or abnormal keratan sulfate.

  • Congenital Macular Corneal Dystrophy

    early onset macular corneal dystrophy, typically occurring in childhood.

Patient EducationClinical

Lattice corneal dystrophy type I

Lattice corneal dystrophy type I is an eye disorder that affects the clear, outer covering of the eye called the cornea. The cornea must remain clear for an individual to see properly; however, in lattice corneal dystrophy type I, protein clumps known as amyloid deposits cloud the cornea, which leads to vision impairment.

Read the full article at MedlinePlus

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

Code History & ChangesHistory

Replacement H18.549 replaces the following previously assigned code(s):

  • H18.54 - Lattice corneal dystrophy
FY 2021AddedAdded to the ICD-10-CM code setEffective October 1, 2020.
FY 2022–2025No changes
FY 2026CurrentCurrent code set, no changesEffective October 1, 2025 through September 30, 2026.

Questions About H18.549Overview

Is H18.549 (Lattice corneal dystrophy) a billable code?

Yes. This is a billable ICD-10-CM code, specific enough to report lattice corneal dystrophy, unspecified eye on HIPAA-covered claims from October 1, 2025 through September 30, 2026.

What MS-DRG does H18.549 group to?

When lattice corneal dystrophy, unspecified eye is the principal diagnosis on an inpatient stay, it groups to MS-DRG 124, 125, with relative weights from 0.7678 to 1.3231 depending on complications. Higher weights mean higher Medicare reimbursement.

Footnotes

[1] Not chronic - A diagnosis code that does not fit the criteria for chronic condition (duration, ongoing medical treatment, and limitations) is considered not chronic. Some codes designated as not chronic are acute conditions. Other diagnosis codes that indicate a possible chronic condition, but for which the duration of the illness is not specified in the code description (i.e., we do not know the condition has lasted 12 months or longer) also are considered not chronic.