craniofacial disease (Q17122): Difference between revisions

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Created a new Item: craniofacial disease, human disease
 
Created claim: exact match (P409): http://www.orpha.net/ORDO/Orphanet_98038
 
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Property / instance of
 
Property / instance of: developmental defect during embryogenesis / rank
 
Normal rank
Property / instance of
 
Property / instance of: class of disease / rank
 
Normal rank
Property / subclass of
 
Property / subclass of: disease / rank
 
Normal rank
Property / subclass of
 
Property / subclass of: developmental defect during embryogenesis / rank
 
Normal rank
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
  • cranial malformation

Statements