Analphalipoproteinaemia (Q97098)
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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. |
Statements
CID11:ID_1796662502
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