lactose intolerance (Q18620): Difference between revisions

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Changed claim: has cause (P74): absence (Q1401)
Created claim: exact match (P409): http://www.orpha.net/ORDO/Orphanet_319681
 
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Property / has cause: absence / qualifier
 
Property / health specialty
 
Property / health specialty: endocrinology / rank
 
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Property / symptoms and signs
 
Property / symptoms and signs: abdominal pain / rank
 
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Property / symptoms and signs
 
Property / symptoms and signs: flatulence / rank
 
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Property / symptoms and signs
 
Property / symptoms and signs: diarrhea / rank
 
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Property / symptoms and signs
 
Property / symptoms and signs: bloating / rank
 
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Property / symptoms and signs
 
Property / symptoms and signs: borborygmus / rank
 
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Property / exact match
 
Property / exact match: http://purl.obolibrary.org/obo/DOID_10604 / rank
 
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Property / exact match
 
Property / exact match: http://identifiers.org/doid/DOID:10604 / rank
 
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Property / exact match
 
Property / exact match: http://purl.obolibrary.org/obo/HP_0004789 / rank
 
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Property / exact match
 
Property / exact match: http://www.orpha.net/ORDO/Orphanet_319681 / rank
 
Normal rank

Latest revision as of 09:07, 5 January 2024

condition involving a decreased ability to digest lactose due to a lack of lactase in the small intestines, either genetically or from injury
  • Disaccharide Intolerance 3
  • Hypolactasia, Adult Type
  • LACTOSE INTOLERANCE, ADULT TYPE
  • lactose malabsorption
  • lactase persistence
  • adult lactase deficiency
  • LM
  • lactose intolerant
Language Label Description Also known as
English
lactose intolerance
condition involving a decreased ability to digest lactose due to a lack of lactase in the small intestines, either genetically or from injury
  • Disaccharide Intolerance 3
  • Hypolactasia, Adult Type
  • LACTOSE INTOLERANCE, ADULT TYPE
  • lactose malabsorption
  • lactase persistence
  • adult lactase deficiency
  • LM
  • lactose intolerant

Statements