ICD-10-CM Code H35.52
Pigmentary retinal dystrophy
Billable CodeBillable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.
H35.52 is a billable ICD code used to specify a diagnosis of pigmentary retinal dystrophy. A 'billable code' is detailed enough to be used to specify a medical diagnosis.
The ICD code H355 is used to code Stargardt disease
Stargardt disease, or fundus flavimaculatus, is an inherited form of juvenile macular degeneration that causes progressive vision loss usually to the point of legal blindness. Several genes are associated with the disorder. Symptoms, mainly vision loss, typically develop before age 20, and also include wavy vision, blind spots, blurriness, impaired color vision, and difficulty adapting to dim lighting.
|MeSH Codes:||, , D052245|
|ICD 9 Codes:||, 362.76,|
Coding Notes for H35.52 Info for medical coders on how to properly use this ICD-10 code
Inclusion TermsInclusion Terms are a list of concepts for which a specific code is used. The list of Inclusion Terms is useful for determining the correct code in some cases, but the list is not necessarily exhaustive.
- Albipunctate retinal dystrophy
- Retinitis pigmentosa
- Tapetoretinal dystrophy
- DRG Group #124-125 - Other disorders of the eye with MCC.
- DRG Group #124-125 - Other disorders of the eye without MCC.
Related Concepts SNOMET-CT
- Early onset cerebellar ataxia with retinitis pigmentosa and optic atrophy (disorder)
ICD-10-CM Alphabetical Index References for 'H35.52 - Pigmentary retinal dystrophy'
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code H35.52. Click on any term below to browse the alphabetical index.
Equivalent ICD-9 Code GENERAL EQUIVALENCE MAPPINGS (GEM)
This is the official exact match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that in all cases where the ICD9 code 362.74 was previously used, H35.52 is the appropriate modern ICD10 code.