craniofacial disease (Q17122): Difference between revisions
Jump to navigation
Jump to search
Created claim: subclass of (P1): developmental defect during embryogenesis (Q13937) |
Created claim: exact match (P409): http://www.orpha.net/ORDO/Orphanet_98038 |
||
| Property / exact match | |||
| Property / exact match: http://www.orpha.net/ORDO/Orphanet_98038 / rank | |||
Normal rank | |||
Latest revision as of 20:34, 29 December 2023
human disease
- cranial malformation
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | craniofacial disease |
human disease |
|