Intestinal disaccharidase deficiency
Intestinal disaccharidase deficiency
Definition
Inherited or acquired disorders of sugar metabolism. Deficiencies of lactase, maltase or sucrase-isomaltase usually occur irreversibly and independent of one another. Congenital deficiencies are rare whereas acquired deficiencies are more common and may be seen following intestinal mucosal brush-border injury. Clinical signs include abdominal cramping, bloating, flatulence and diarrhea following dietary intake of lactose, maltose or sucrose. The clinical course leads to malabsorption of disaccharides which has implications for normal growth and development if manifested at an early age.
Also known as intestinal disaccharidase deficiency and disaccharide malabsorption — per MONDO
Also identified as
- DOID 9868 per MONDO
- ICD9 271.3 per MONDO
- NCIT C34731 per MONDO
- SCTID 22169002 per MONDO
- UMLS C0699848 per MONDO
Affected Organs
| Organ | Involvement | Source |
|---|---|---|
| Alimentary part of gastrointestinal system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Alimentary part of gastrointestinal system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Intestine | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Intestine | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Small intestine | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Small intestine | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |