retinitis pigmentosa 59 (Q27677752)
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A retinitis pigmentosa that has material basis in mutation in the DHDDS gene on chromosome 1p36.11.
- RP59
- RETINITIS PIGMENTOSA 59
- RETINITIS PIGMENTOSA 59; RP59
- retinitis pigmentosa type 59
- Congenital disorder of glycosylation type Ibb
- CDG1BB
- DHDDS-CDG
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | retinitis pigmentosa 59 |
A retinitis pigmentosa that has material basis in mutation in the DHDDS gene on chromosome 1p36.11. |
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Statements
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Identifiers
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