Dementia due to genetic causes (Q90896)
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Dementia that is due to cerebral infarcts associated with a genetic mutations. They can be autosomal dominant (such as CADASIL due to Notch3 mutation) or autosomal recessive (such as CARASIL due to HTRA1 mutation).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1957030048 |
||
| English | Dementia due to genetic causes |
Dementia that is due to cerebral infarcts associated with a genetic mutations. They can be autosomal dominant (such as CADASIL due to Notch3 mutation) or autosomal recessive (such as CARASIL due to HTRA1 mutation). |
Statements
CID11:ID_1957030048
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dki-india-ID_1957030048
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Concluído
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