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Metadata
ID DOID:0111633
Name congenital sucrase-isomaltase deficiency
Definition A carbohydrate metabolic disorder characterized by malabsorption of oligosaccharides and disaccharides that has_material_basis_in homozygous or compound heterozygous mutation in SI on chromosome 3q26.1.
https://ghr.nlm.nih.gov/condition/congenital-sucrase-isomaltase-deficiency, https://www.ncbi.nlm.nih.gov/pubmed/3925457
Xrefs

GARD:7710

ICD10CM:E74.31

MEDDRA:10066387

MESH:C538139

MIM:222900

NCI:C128190

ORDO:35122

SNOMEDCT_US_2023_03_01:78373000

UMLS_CUI:C1283620

Subsets

DO_rare_slim

NCIthesaurus

Synonyms

congenital sucrase-isomaltose malabsorption [EXACT]

congenital sucrose intolerance [EXACT]

CSID [EXACT]

disaccharide intolerance [EXACT]

SI deficiency [EXACT]

Parent Relationships

is_a carbohydrate metabolic disorder

is_a physical disorder

is_a autosomal recessive disease

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