Item:Q17592: Difference between revisions

Created a new Item: metabolic disease associated with ocular features, human disease
 
Created claim: exact match (P409): http://www.orpha.net/ORDO/Orphanet_98710
 
(2 intermediate revisions by the same user not shown)
Property / instance of
 
Property / instance of: class of disease / rank
 
Normal rank
Property / subclass of
 
Property / subclass of: rare genetic eye disease / rank
 
Normal rank
Property / exact match
 
Property / exact match: http://www.orpha.net/ORDO/Orphanet_98710 / rank
 
Normal rank