trehalase deficiency
This syndrome is characterised by diarrhoea and vomiting after ingestion of trehalose, a disaccharide found mainly in mushrooms
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trehalase deficiency
Summary
trehalase deficiency is a class of disease[1].
Key Facts
- trehalase deficiency's instance of is recorded as class of disease[2].
- trehalase deficiency's subclass of is recorded as metabolic disease with intestinal involvement[3].
- trehalase deficiency's subclass of is recorded as disorder of carbohydrate absorption and transport[4].
- trehalase deficiency's subclass of is recorded as congenital intestinal disease due to an enzymatic defect[5].
- trehalase deficiency's MeSH descriptor ID is recorded as C562603[6].
- trehalase deficiency's OMIM ID is recorded as 612119[7].
- trehalase deficiency's ICD-10 ID is recorded as E74.3[8].
- trehalase deficiency's KEGG ID is recorded as H02090[9].
- trehalase deficiency's Orphanet ID is recorded as 103909[10].
- trehalase deficiency's ICD-9-CM is recorded as 271.8[11].
- trehalase deficiency's genetic association is recorded as TREH[12].
- trehalase deficiency's UMLS CUI is recorded as C0268187[13].
- trehalase deficiency's ICD-10-CM is recorded as E74.3[14].
- trehalase deficiency's PatientsLikeMe condition ID is recorded as trehalase-deficiency[15].
- trehalase deficiency's GARD rare disease ID is recorded as 10372[16].
- trehalase deficiency's Mondo ID is recorded as MONDO_0012803[17].
- trehalase deficiency's UniProt disease ID is recorded as DI-05182[18].