2008 ICD-9-CM Volume 1 Diagnosis Codes Home > Diseases Of The Nervous System And Sense Organs 320-389 > Disorders Of The Eye And Adnexa 360-379 > Other Retinal Disorders 362.* >  2008 ICD-9-CM Diagnosis 362.74
Pigmentary retinal dystrophy On October 1, 2008 the 2009 ICD-9-CM codes came into effect. Therefore, this code may be out of date.
The 2009 version of ICD-9-CM 362.74 can be accessed here. - Hereditary, progressive degeneration of the neuroepithelium of the retina characterized by night blindness and progressive contraction of the visual field.
- 362.74 is a specific code that can be used to specify a diagnosis
- 362.74 contains 8 index entries
- View the ICD-9-CM Volume 1 362.* hierarchy
362.74 also known as:- Retinal dystrophy, albipunctate
- Retinitis pigmentosa
Index entries containing 362.74:- Degeneration, degenerative
- retina (peripheral) 362.60
- pigmentary (primary)
 362.74
- tapetoretinal 362.74
- adult or presenile form 362.50
Dystrophy, dystrophia 783.9- retina, retinal (hereditary) 362.70
- albipunctate 362.74
- pigmentary 362.74
- tapetoretinal NEC 362.74
Pigmentation (abnormal) 709.00- retina (congenital) (grouped) (nevoid) 743.53
- acquired 362.74
Retinitis (see also Chorioretinitis) 363.20- pigmentosa 362.74
Retinopathy (background) 362.10- pigmentary, congenital 362.74
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