ICD10
ICD-10 Code H31.2: Hereditary choroidal dystrophy
Reviewed by HealthAssure Clinical TeamUpdated 26 May 2026
What is this code?
ICD-10 entries help standardize how diagnoses are organized for coding, reporting, analytics, and documentation. This code sits within the broader ICD-10 area for Diseases of the eye and adnexa (H00-H59).
When is it used?
- May be used when a clinician documents hereditary choroidal dystrophy in a patient's medical record.
- May appear in hospital records, claims, referrals, and clinical documentation.
- This code may act more like a grouping or parent code, so a more specific child code may be used in final documentation when available.
What it does not mean
- A code alone does not explain severity, treatment plan, or outcome.
- A medical code should not be treated as a substitute for a doctor's diagnosis or advice.
- This entry may represent a broader category rather than the most specific billable code.
Code hierarchy
chapter
7Diseases of the eye and adnexa (H00-H59)
block
H30-H36Disorders of choroid and retina
category
H31Other disorders of choroid
currentH31
Official coding notes
Excludes2 (may code together if documented)
- hyperornithinemia (E72.4)
- ornithinemia (E72.4)
Where you may see this code
You may see this entry in coding references, medical records, or claims workflows when a broader diagnosis category is being reviewed before a more specific code is chosen.
Related specialists
Ophthalmologist
Related codes
Sibling codes
Mapped diagnoses and classifications
SNOMED_CT 312927001high
Bietti's crystalline retinopathy
Source: SNOMED International ICD-10 map
SNOMED_CT 15989831000119105high
Bilateral choroideremia of eyes
Source: SNOMED International ICD-10 map
SNOMED_CT 231996009high
Central areolar choroidal sclerosis
Source: SNOMED International ICD-10 map
SNOMED_CT 75241009high
Choroideremia
Source: SNOMED International ICD-10 map
SNOMED_CT 314467007high
Gyrate atrophy
Source: SNOMED International ICD-10 map
SNOMED_CT 724384008high
Helicoid peripapillary chorioretinal degeneration
Source: SNOMED International ICD-10 map
Coding guidelines
Compatibility
Legacy code aligns to an official FY 2026 category. Frontend should resolve to the official category page and surface the billable child codes.
Legacy codes
H31.2
Replacement codes
H31.20 — Hereditary choroidal dystrophy, unspecifiedH31.21 — ChoroideremiaH31.22 — Choroidal dystrophy (central areolar) (generalized) (peripapillary)H31.23 — Gyrate atrophy, choroidH31.29 — Other hereditary choroidal dystrophy
Common synonyms
Hereditary choroidal dystrophy
Frequently asked questions
About this content
This page is prepared by HealthAssure's clinical team using official coding standards from ICD-10. AI tools assist with drafting explanations, which are then reviewed and verified by healthcare professionals for accuracy. This content is for informational purposes and does not replace professional medical advice. Meet our team.