Crouzon syndrone (Q17116): Difference between revisions
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Created claim: subclass of (P1): craniosynostosis (Q17117) |
Created claim: exact match (P409): http://www.orpha.net/ORDO/Orphanet_207 |
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| Property / subclass of | |||
| Property / subclass of: craniostenosis associated with a strabismus / rank | |||
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| Property / subclass of | |||
| Property / subclass of: syndromic craniosynostosis / rank | |||
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| Property / subclass of: disease / rank | |||
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| Property / health specialty | |||
| Property / health specialty: medical genetics / rank | |||
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| Property / exact match | |||
| Property / exact match: http://purl.obolibrary.org/obo/DOID_2339 / rank | |||
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| Property / exact match | |||
| Property / exact match: http://identifiers.org/doid/DOID:2339 / rank | |||
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| Property / exact match | |||
| Property / exact match: http://purl.obolibrary.org/obo/HP_0004439 / rank | |||
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| Property / exact match | |||
| Property / exact match: http://www.orpha.net/ORDO/Orphanet_207 / rank | |||
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Latest revision as of 20:48, 29 December 2023
Congenital disorder of the skull and face
- Craniofacial Dysostosis
- Crouzon's disease
- Craniofacial dysostosis type 1
- CROUZON SYNDROME
- CFD1
- Craniofacial Dysostosis, Type 1
- Crouzon craniofacial dysostosis
- Crouzon disease
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Crouzon syndrone |
Congenital disorder of the skull and face |
|