H35.5 is the ICD-10 code for Hereditary retinal dystrophy. It is a four-character subcategory of H35 (Other retinal disorders), the most specific level in the WHO edition. It belongs to the block H30–H36 (Disorders of choroid and retina) in Chapter VII, Diseases of the eye and adnexa.
- Code type
- Subcategory (4 characters)
- Chapter
- VII · H00–H59
- Classification
- WHO ICD-10, 2019 version
What H35.5 includes
Conditions and terms that are coded here.
- Dystrophy:
- retinal (albipunctate)(pigmentary)(vitelliform)
- tapetoretinal
- vitreoretinal
- Retinitis pigmentosa
- Stargardt disease
H35.5 in national editions
Countries report with their own edition of ICD-10. Most keep the WHO code and add more specific codes beneath it.
H35.5Hereditär retinaldystrofi
- H35.5AVitreoretinal dystrofi
- H35.5BRetinitis pigmentosa-liknande tillstånd
- H35.5CPigmentepiteldystrofi
- H35.5WAnnan ärftlig retinal dystrofi
- H35.5XÄrftlig retinal dystrofi, ospecificerad
H35.5Arvelig netthinnedystrofi
DH355Familiær retinadystrofi
- DH355ADystrophia retinae albi punctata
- DH355BDystrophia tapetoretinalis
- DH355CDystrophia retinae vitelliformis
- DH355DDystrophia vitreo retinalis
- DH355EDystrophia retinae pigmentaria
- DH355FStargardts sygdom
H35.5Perinnöllinen verkkokalvorappeuma
H35.5Hereditäre Netzhautdystrophie
H35.5Dystrophie rétinienne héréditaire
H35.5hereditaire retinadystrofie
Listed through more specific codes:
- H35.50Unspecified hereditary retinal dystrophy
- H35.51Vitreoretinal dystrophy
- H35.52Pigmentary retinal dystrophy
- H35.53Other dystrophies primarily involving the sensory retina
- H35.54Dystrophies primarily involving the retinal pigment epithelium
Based on the World Health Organization’s International Statistical Classification of Diseases and Related Health Problems, 10th revision (ICD-10), 2019 version, and the national editions published by each country’s health authority. This page is a reference, not coding advice; follow your national coding rules when you report.
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