primary bone dysplasia (Q22011): Difference between revisions
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Created claim: instance of (P2): developmental defect during embryogenesis (Q13937) |
Created claim: exact match (P409): http://www.orpha.net/ORDO/Orphanet_364526 |
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| Property / instance of | |||
| Property / instance of: class of disease / rank | |||
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| Property / subclass of | |||
| Property / subclass of: rare genetic bone development disorder / rank | |||
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| Property / subclass of | |||
| Property / subclass of: rare genetic bone disease / rank | |||
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| Property / exact match | |||
| Property / exact match: http://www.orpha.net/ORDO/Orphanet_364526 / rank | |||
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Latest revision as of 20:29, 12 April 2024
human disease
- Primary osteodysplasia
- Primary skeletal dysplasia
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | primary bone dysplasia |
human disease |
|