Gaucher's disease type I (Q32145230)
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Gaucher's disease characterized by absence of primary central nervous system involvement that has material basis in a mutation of GBA on chromosome 1q22
- Acid Beta-Glucosidase Deficiency
- Gba Deficiency
- Gaucher Disease, Noncerebral Juvenile
- GD I
- Glucocerebrosidase Deficiency
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Gaucher's disease type I |
Gaucher's disease characterized by absence of primary central nervous system involvement that has material basis in a mutation of GBA on chromosome 1q22 |
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Statements
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Identifiers
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