Item:Q17577: Difference between revisions

Created a new Item: rare genetic endocrine disease, form of endocrine system disease that is both rare and inborn
 
Created claim: exact match (P409): http://www.orpha.net/ORDO/Orphanet_156638
 
(3 intermediate revisions by the same user not shown)
Property / instance of
 
Property / instance of: class of disease / rank
 
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Property / subclass of
 
Property / subclass of: rare genetic disease / rank
 
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Property / subclass of
 
Property / subclass of: endocrine system disease / rank
 
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Property / exact match
 
Property / exact match: http://www.orpha.net/ORDO/Orphanet_156638 / rank
 
Normal rank