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2007 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.* > 2007 ICD-9-CM Diagnosis 362.73 Vitreoretinal dystrophies  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 Therefore, this code may be out of date.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 362.73 can be accessed here. X chromosome recessive disorder, found nearly exclusively in males and becoming apparent around puberty. Characterized initially by a cystlike structure involving the FOVEA CENTRALIS, a peripheral retinoschisis occurs in about half the patients. 362.73 is a specific code that can be used to specify a diagnosis 362.73 contains 3 index entries View the ICD-9-CM Volume 1 362.* hierarchy 362.73 also known as: Juvenile retinoschisis Index entries containing 362.73: Degeneration, degenerative vitreoretinal (primary) 362.73 secondary 362.66 Dystrophy, dystrophia 783.9 vitreoretinal (primary) 362.73 secondary 362.66 Retinoschisis 361.10 juvenile 362.73