MSeqDR Mitochondrial Disease Portal


 
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Parent Node:
expandintestinal disease (MONDO:0005020)
Parent Node:
expandmetabolic disease (MONDO:0005066)
..Starting node
..expandmetabolic disease with intestinal involvement ()

       Child Nodes:
........expand4-hydroxyphenylacetic aciduria ()
........expandabetalipoproteinemia ()
........expandacrodermatitis enteropathica ()
........expandchronic diarrhea due to glucoamylase deficiency ()
........expandchronic diarrhea with villous atrophy ()  LSDB  L: 00164;
........expandchronic granulomatous disease ()
........expandchylomicron retention disease ()
........expandcollagenous sprue ()
........expandcongenital disorder of glycosylation with intestinal involvement ()
........expandcongenital lactase deficiency ()
........expanddiarrhea-vomiting due to trehalase deficiency ()
........expandglucose-galactose malabsorption ()
........expandhereditary folate malabsorption ()
........expandhereditary fructose intolerance ()
........expandidiopathic malabsorption due to bile acid synthesis defects ()
........expandImerslund-Grasbeck syndrome ()
........expandintestinal disaccharidase deficiency ()
........expandlactose intolerance (disease) ()
........expandmitochondrial DNA depletion syndrome ()
........expandmitochondrial neurogastrointestinal encephalomyopathy ()
........expandPearson syndrome ()  LSDB  L: 00169;



 Sister Nodes: 
..expandacquired metabolic disease ()
..expandbilirubin metabolism disease ()
..expandcarbohydrate metabolism disease ()
..expandcarotenemia ()
..expandchondrocalcinosis ()
..expandcomplement deficiency ()
..expanddevelopmental anomaly of metabolic origin ()
..expanddiabetic nephropathy ()
..expanddiabetic retinopathy ()
..expanddisorder of acid-base balance ()
..expanddisorder of glycosylation ()
..expanddisorder of organic acid metabolism ()
..expandDNA repair disease ()
..expandfamilial thyroid dyshormonogenesis ()
..expandglucose metabolism disease ()
..expandglutaric aciduria (disease) ()
..expandgout ()
..expandhemolytic anemia due to an erythrocyte nucleotide metabolism disorder ()
..expandhyperlipidemia (disease) ()
..expandhyperlipoproteinemia ()
..expandhypermanganesemia with dystonia ()
..expandhypertriglyceridemia (disease) ()
..expandhypoalphalipoproteinemia ()
..expandinborn errors of metabolism ()
..expandlactic acidosis ()
..expandlipodystrophy (disease) ()
..expandmetabolic disease with epilepsy ()
..expandmetabolic disease with intestinal involvement ()
..expandmetabolic disease with skin involvement ()
..expandmetabolic syndrome ()
..expandmineral metabolism disease ()
..expandporphyrin metabolism disease ()
..expandproteostasis deficiencies ()
..expandpurine metabolism disease ()
..expandpyrimidine metabolism disease ()
..expandsteroid metabolism disease ()
..expandthiopurine metabolic disease ()
..expandvitamin B12 deficiency ()
..expandxanthinuria ()
..expandxanthoma (disease) ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:15188
Name:metabolic disease with intestinal involvement
Definition:A metabolic disease that involves the intestine.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:intestine metabolic disease; metabolic disease of intestine
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
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