Analphalipoproteinaemia (Q97098): Difference between revisions
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Revision as of 13:08, 16 August 2026
Tangier disease is a recessively inherited hypoalphalipopproteinaemia characterised by cholesterol deposition in the cornea, tonsils, rectum, liver and spleen, and sometimes associated with neurologic symptoms.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1796662502 |
||
| English | Analphalipoproteinaemia |
Tangier disease is a recessively inherited hypoalphalipopproteinaemia characterised by cholesterol deposition in the cornea, tonsils, rectum, liver and spleen, and sometimes associated with neurologic symptoms. |
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CID11:ID_1796662502
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dki-india-ID_1796662502
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Concluído
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