ocular albinism with sensorineural deafness (Q50357711)
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human disease
- WS2-OA
- autosomal recessive Waardenburg syndrome type 2 with ocular albinism
- digenic Waardenburg syndrome/ocular albinism
- digenic Waardenburg syndrome/albinism
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | ocular albinism with sensorineural deafness |
human disease |
|
Statements
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Identifiers
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