rare parenchymal liver disease (Q17371): Difference between revisions

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Created a new Item: rare parenchymal liver disease, human disease
 
Created claim: exact match (P409): http://www.orpha.net/ORDO/Orphanet_101939
 
(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 hepatic disease / rank
 
Normal rank
Property / exact match
 
Property / exact match: http://www.orpha.net/ORDO/Orphanet_101939 / rank
 
Normal rank

Latest revision as of 16:45, 30 December 2023

human disease
Language Label Description Also known as
English
rare parenchymal liver disease
human disease

    Statements