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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
autoimmune enteropathy +  
Autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome 
blind loop syndrome 
celiac disease  
congenital disorder of deglycosylation 1 
disorder of carbohydrate transmembrane transport and absorption +  
disorder of fructose metabolism +  
disorder of galactose and fructose metabolism +  
disorder of galactose metabolism +  
disorder of gluconeogenesis +  
disorder of glycogen metabolism +  
disorder of glycolysis +  
disorders of pentose/polyol metabolism +  
eating disorder +   
Genetic intestinal disease due to fat malabsorption 
glucosephosphate dehydrogenase deficiency 
Gräsbeck-Imerslund disease 
hemorrhagic disease of newborn 
hereditary folate malabsorption 
hyperinsulinemic hypoglycemia +  
intestinal disaccharide deficiency and disaccharide malabsorption +  
lactose intolerance +  
Inability to fully digest and absorb lactose due to limited or no lactase activity in the small intestine. Congenital intolerance is inherited following an autosomal recessive pattern but is rare. It is more often due to a gradual decline of lactase production in adulthood following the ingestion of fewer lactose-containing foods or secondary to an intestinal mucosal brush-border injury. Prevalence is highest among Asians, Native Americans and Africans. Clinical signs include abdominal cramping, bloating, flatulence and diarrhea following the dietary intake of lactose.
malnutrition 
mucopolysaccharidosis +  
multiple carboxylase deficiency +  
nutritional deficiency disease +  
oligosaccharidosis +  
overnutrition +   
potassium deficiency disease +  
primary hyperoxaluria +  
pyruvate dehydrogenase deficiency +  
tropical sprue 

Synonyms
Exact Synonyms: DOID:10604 ;   LM - lactose malabsorption ;   NCIT:C3154 ;   http://identifiers.org/medgen/6001 ;   http://identifiers.org/mesh/D007787 ;   http://identifiers.org/snomedct/267425008 ;   http://linkedlifedata.com/resource/umls/id/C0022951 ;   http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1026224967 ;   lactose intolerance (disease)
Related Synonyms: lactase persistence
Xrefs: DOID:10604 ;   HP:0004789 ;   ICD10:E73 ;   ICD9:271.3 ;   MEDGEN:6001 ;   MESH:D007787 ;   MONDO:0100345 ;   MedDRA:10023681 ;   NCI:C3154 ;   SCTID:267425008

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