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ICD-10-CM Code H35.50
Unspecified hereditary retinal dystrophy

Billable Code
Billable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.
| ICD-10 from 2011 - 2016

H35.50 is a billable ICD code used to specify a diagnosis of unspecified hereditary 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.

Specialty: Ophthalmology
MeSH Codes: , , D052245
ICD 9 Codes: , 362.76,
Source: Wikipedia

MS-DRG Mapping

  • 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

  • Stargardt's disease (disorder)

ICD-10-CM Alphabetical Index References for 'H35.50 - Unspecified hereditary retinal dystrophy'

The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code H35.50. Click on any term below to browse the alphabetical index.


Hereditary retinal dystrophy, unspecified (exact match)

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 362.70 was previously used, H35.50 is the appropriate modern ICD10 code.

Parent Code: H35.5 - Hereditary retinal dystrophy

** This Document Provided By ICD.Codes **
Source: http://icd.codes/icd10cm/H3550