Familial hypomagnesaemia - hypercalciuria - nephrocalcinosis - severe ocular involvement (Q99737): Difference between revisions
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Hipomagnesemia primária familiar - hipercalciúria - nefrocalcinose - envolvimento ocular grave é uma forma de hipomagnesemia primária familiar, caracterizada por perda renal excessiva de magnésio e cálcio, nefrocalcinose bilateral, insuficiência renal progressiva e anormalidades oculares graves. | |||||||||||||||
| description / en | description / en | ||||||||||||||
Familial primary hypomagnesemia - hypercalciuria - nephrocalcinosis - severe ocular involvement is a form of familial primary hypomagnesemia, characterised by excessive magnesium and calcium renal wasting, bilateral nephrocalcinosis, progressive renal failure and severe ocular abnormalities. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/154680834 / rank | |||||||||||||||
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CID11:ID_154680834 | |||||||||||||||
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dki-india-ID_154680834 | |||||||||||||||
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| Property / Verification Status: Concluído / rank | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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15 August 2026
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| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
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Latest revision as of 16:24, 16 August 2026
Familial primary hypomagnesemia - hypercalciuria - nephrocalcinosis - severe ocular involvement is a form of familial primary hypomagnesemia, characterised by excessive magnesium and calcium renal wasting, bilateral nephrocalcinosis, progressive renal failure and severe ocular abnormalities.
| Language | Label | Description | Also known as |
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| default for all languages | ID_154680834 |
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| English | Familial hypomagnesaemia - hypercalciuria - nephrocalcinosis - severe ocular involvement |
Familial primary hypomagnesemia - hypercalciuria - nephrocalcinosis - severe ocular involvement is a form of familial primary hypomagnesemia, characterised by excessive magnesium and calcium renal wasting, bilateral nephrocalcinosis, progressive renal failure and severe ocular abnormalities. |
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CID11:ID_154680834
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dki-india-ID_154680834
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Concluído
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15 August 2026
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