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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