rare teratologic disease (Q14040): Difference between revisions

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Created a new Item: rare teratologic disease, human disease
 
Created claim: exact match (P409): http://www.orpha.net/ORDO/Orphanet_52662
 
(4 intermediate revisions by the same user not shown)
Property / instance of
 
Property / instance of: developmental defect during embryogenesis / rank
 
Normal rank
Property / instance of
 
Property / instance of: class of disease / rank
 
Normal rank
Property / subclass of
 
Property / subclass of: developmental defect during embryogenesis / rank
 
Normal rank
Property / subclass of
 
Property / subclass of: embryofetopathy / rank
 
Normal rank
Property / exact match
 
Property / exact match: http://www.orpha.net/ORDO/Orphanet_52662 / rank
 
Normal rank

Latest revision as of 09:53, 6 August 2023

human disease
  • Acquired embryofetopathy
Language Label Description Also known as
English
rare teratologic disease
human disease
  • Acquired embryofetopathy

Statements