2026 ICD-10-CM Diagnosis Code H35.51Vitreoretinal dystrophy
ICD-10-CM Codes›H00–H59›H30-H36›H35
- Billable — Valid for Submission
- Chronic Condition
H35.51 is a billable ICD-10-CM diagnosis code for vitreoretinal dystrophy. 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. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Retinal and vitreous conditions.
Code Identity
Code Classification
Approximate SynonymsGuidance
Alternate terms and clinical phrases that map to this code.
- Atrophy of bilateral eyes
- Autosomal dominant neovascular inflammatory vitreoretinopathy
- Autosomal dominant vitreoretinochoroidopathy
- Bilateral orbital soft tissue atrophy
- Bilateral vitreoretinal tuft of eyes
- Bilateral vitreous degeneration of eyes
- Familial exudative vitreoretinopathy
- Goldmann-Favre syndrome
- Hereditary vitreoretinopathy
- Left orbital soft tissue atrophy
- Peripheral degeneration of retina of bilateral eyes
- Peripheral retina - white with pressure
- Peripheral retina - white without pressure
- Peripheral snowflake retinal degeneration
- Right orbital soft tissue atrophy
- Snowflake retinal degeneration
- Vitreoretinal degeneration
- Vitreoretinal dystrophy
- Vitreoretinal tuft
- Vitreoretinal tuft of left eye
- Vitreoretinal tuft of right eye
- Wagner syndrome
Index to Diseases and InjuriesGuidance
Alphabetical index entries that point to this code.
- retinal (hereditary) - H35.50
- vitreoretinal - H35.51
- vitreoretinal - H35.51
External Cause of Injuries IndexGuidance
References for this code in the External Cause of Injuries Index.
- Dystrophy, dystrophia
- retinal (hereditary)
- vitreoretinal
- Dystrophy, dystrophia
- vitreoretinal
Clinical ClassificationClinical
AHRQ’s CCSR groups this code into broader clinical categories.
Clinical InformationClinical
Hereditary Retinal Dystrophy
an inherited form of retinal dystrophy.
Patient EducationClinical
Retinal Disorders
The retina is a layer of tissue in the back of your eye that senses light and sends images to your brain. In the center of this nerve tissue is the macula. It provides the sharp, central vision needed for reading, driving and seeing fine detail.
Read the full article at MedlinePlus
Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.
Convert H35.51 to ICD-9-CMHistory
The closest ICD-9-CM equivalents under the General Equivalence Mappings.
Code HistoryHistory
Questions About H35.51Overview
Is H35.51 (Hereditary retinal dystrophy) a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report vitreoretinal dystrophy on HIPAA-covered claims from October 1, 2025 through September 30, 2026.
What MS-DRG does H35.51 group to?
When vitreoretinal dystrophy 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.
What is the ICD-9 equivalent of H35.51?
Under the General Equivalence Mappings, vitreoretinal dystrophy converts to ICD-9-CM 362.73 (vitreoretinal dystrophy). The mapping is a direct match.
Footnotes
[1] Chronic - a chronic condition code indicates a condition lasting 12 months or longer and its effect on the patient based on one or both of the following criteria:
- The condition results in the need for ongoing intervention with medical products,treatment, services, and special equipment
- The condition places limitations on self-care, independent living, and social interactions.
