Item:Q16261: Difference between revisions
Created a new Item: rare genetic developmental defect during embryogenesis, human disease |
Created claim: exact match (P409): http://www.orpha.net/ORDO/Orphanet_183530 |
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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 disease / rank | |||
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| Property / exact match | |||
| Property / exact match: http://www.orpha.net/ORDO/Orphanet_183530 / rank | |||
Normal rank | |||