H31.2 - Hereditary choroidal dystrophy
- Applicable to Hereditary choroidal dystrophy
- The 2025 edition of ICD10-CM H31.2 became effective on October 1, 2024.
- This is the American ICD10-CM version of H31.2 - other international versions of ICD10 H31.2 may differ.
- H31.2 is a Non-Billable / Non-Specific ICD10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- H31.2 Code should not be used for billing or reimbursement purposes as there are multiple ICD-10 CM codes below it that contain a greater level of detail.
- H31.2 - Hereditary choroidal dystrophy
- H31.2 - Hereditary choroidal dystrophy
- H31.20 - Hereditary choroidal dystrophy, unspecified
- H31.21 - Choroideremia
- H31.22 - Choroidal dystrophy (central areolar) (generalized) (peripapillary)
- H31.23 - Gyrate atrophy, choroid
- H31.29 - Other hereditary choroidal dystrophy
Type 2 Excludes
- hyperornithinemia (E72.4)
- ornithinemia (E72.4)
Non-Billable/Non-Specific Code
The following codes above H31.2 contain annotation back-references that may be applicable to H31.2:
- Chapter: H00-H59 - Diseases of the eye and adnexa
- Section: H30-H36 - Disorders of choroid and retina
- Category: H31 - Other disorders of choroid
Browse other similar CM codes:
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
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