Oculocerebrorenal syndrome (Q40012): Difference between revisions
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Síndrome oculocerebrorrenal de Lowe (OCLR) é um transtorno multissistêmico caracterizado por catarata congênita, glaucoma, incapacidade intelectual, deficiência de crescimento pós-natal e disfunção tubular renal com insuficiência renal crônica. | |||
| description / en | description / en | ||
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. | |||
Revision as of 05:39, 13 August 2026
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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 5C60.0 |
||
| English | Oculocerebrorenal syndrome |
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. |
