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5C60.0 Oculocerebrorenal syndrome

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

Oculocerebrorenal syndrome of Lowe (OCRL) is a multisystem disorder characterised by congenital cataracts, glaucoma, intellectual disabilities, postnatal growth retardation and renal tubular dysfunction with chronic renal failure.

synonyms

• Oculocerebrorenal syndrome
• Phosphatidylinositol 4,5-biphosphate 5-phosphatase deficiency
• Lowe oculocerebrorenal syndrome
• Lowe syndrome
• Lowe disease
• Oculocerebrorenal dystrophy
• Cerebro-oculorenal dystrophy
• OCRL1 - [Oculocerebrorenal syndrome]
• Lowe-Terrey-Maclachlan syndrome
• renal-oculocerebrodystrophy
• Glaucoma in Lowe syndrome

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