Item:Q13937: Difference between revisions

Created a new Item: developmental defect during embryogenesis, human disease
 
Created claim: exact match (P409): http://www.orpha.net/ORDO/Orphanet_93890
 
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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: congenital abnormality / rank
 
Normal rank
Property / subclass of: congenital abnormality / qualifier
 
Property / exact match
 
Property / exact match: http://www.orpha.net/ORDO/Orphanet_93890 / rank
 
Normal rank