9B70 Inherited retinal dystrophies
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
inclusions
- Leber congenital amaurosis
- Stargardt disease
- Vitreoretinal dystrophy
code elsewhere
postcoordination
Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Laterality - only one may be selected
synonyms
- Inherited retinal dystrophies
- hereditary retinal dystrophies
- Amaurosis - hypertrichosis
- Autosomal dominant late-onset retinal degeneration
- Bothnia retinal dystrophy
- Västerbotten retinal dystrophy
- Familial flecked retinopathy
- Familial drusen
- Kandori fleck retina
- Retinitis punctata albescens
- Helicoid peripapillary chorioretinal degeneration
- Atrophia areata
- Sveinsson chorioretinal atrophy
- Leber congenital amaurosis
- Leber amaurosis
- MORM syndrome
- Mental retardation - truncal obesity - retinal dystrophy - micropenis
- Intellectual deficit - truncal obesity - retinal dystrophy - micropenis
- Progressive bifocal chorioretinal atrophy
- Stationary retinal dystrophies
- Oguchi disease
- Fundus albipunctatus
- Achromatopsia, complete
- Achromatopsia, incomplete
- Blue cone monochromatism
- Oligocone trichromacy
- X-linked cone dysfunction syndrome with myopia
- Bornholm eye disease
- Progressive retinal dystrophies
- Cone rod dystrophy
- Cone-rod type amaurosis congenita – congenital hypertrichosis
- Progressive cone dystrophy
- Goldmann-Favre syndrome
- Retinal dystrophies with systemic associations
- Senior-Loken syndrome
- McKusick Kaufman syndrome
- Macular Dystrophies
- Stargardt disease
- Fundus flavimaculatus
- FFM - [fundus flavimaculatus]
- Best disease
- Vitelliform macular dystrophy
- Pattern Dystrophies of the RPE
- Vitreoretinal dystrophy
- Autosomal dominant vitreoretinochoroidopathy
- Snowflake vitreoretinal degeneration
- Pigmentary retinal dystrophy
- Retinitis pigmentosa and intellectual deficit due to Xp11.3 deletion
- Retinitis pigmentosa associated with systemic disease
- Retinitis pigmentosa not associated with systemic disease
- Dystrophies primarily involving the retinal pigment epithelium
- Adult-onset foveomacular vitelliform dystrophy
- Butterfly-shaped pigment dystrophy
- Fundus pulverulentus
- Multifocal pattern dystrophy simulating fundus flavimaculatus
- Reticular dystrophy of the retinal pigment epithelium
- Adult vitelliform macula dystrophy
- adult vitelliform macula dystrophy, NOS, atypical
- Albipunctate retinal dystrophy
- Lauber disease
- Behr disease
- Congenital or hereditary macular degeneration
- macular heredodegeneration
- Familial juvenile macular degeneration syndrome
- Congenital retinal blindness
- CRB - [congenital retinal blindness]
- Hereditary retinal degeneration
- hereditary cerebroretinal degeneration
- peripheral hereditary retinal degeneration
- Juvenile hereditary retinal degeneration
- Malattia Leventinese
- Pigmentary degeneration of retina
- pigmentary retinal degeneration
- pigmentary retinopathy
- primary pigmentary degeneration of retina
- retinal depigmentation
- retinal pigment degeneration
- retinopathia pigmentosa without sectoral
- RP - [retinitis pigmentosa]
- Tapetoretinal degeneration
- Tapetoretinal dystrophy
- Vitelliform retinal dystrophy
- vitelliform dystrophy
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