Item:Q17619: Difference between revisions

Created a new Item: rare disorder with dystonia and other neurologic or systemic manifestation, human disease
 
Created claim: exact match (P409): http://www.orpha.net/ORDO/Orphanet_370106
 
(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 dystonia / rank
 
Normal rank
Property / exact match
 
Property / exact match: http://www.orpha.net/ORDO/Orphanet_370106 / rank
 
Normal rank