Search Results

Searched for "Malabsorption Syndromes".

1. hereditary folate malabsorption condition summary
   Related classification: Malabsorption Syndromes

   Related genes:

   • SLC46A1
2. glucose-galactose malabsorption condition summary
   Related classification: Malabsorption Syndromes

   Related genes:

   • SLC5A1
3. lactose intolerance condition summary
   Related classification: Malabsorption Syndromes

   Related genes:

   • LCT
   • MCM6
4. congenital sucrase-isomaltase deficiency condition summary
   Found in link title: Malabsorption Syndromes

   Related genes:

   • SI
5. malabsorption syndrome definition
6. chylomicron retention disease condition summary
   Found in link title: Malabsorption Syndromes

   Related genes:

   • SAR1B
7. abetalipoproteinemia condition summary
   Found in link title: Malabsorption Syndromes

   Related genes:

   • MTTP
8. SLC46A1 gene summary
   Official name: solute carrier family 46 (folate transporter), member 1

   Found related term: ...people with hereditary folate malabsorption. These mutations cause the substitution...
9. lysinuric protein intolerance condition summary
   Found in link title: Malabsorption Syndromes

   Related genes:

   • SLC7A7
10. celiac disease condition summary
    Related classification: Malabsorption Syndromes

    Related genes:

    • HLA-DQA1
    • HLA-DQB1
11. hereditary fructose intolerance condition summary
    Found related term: ...a condition called fructose malabsorption. In people with fructose malabsorption,...

    Related genes:

    • ALDOB
12. intestinal pseudo-obstruction condition summary
    Related term: malabsorption

    Related genes and chromosomes:

    • X chromosome
    • FLNA
13. Shwachman-Diamond syndrome condition summary
    Found related term in link title: Malabsorption

    Related genes:

    • SBDS
14. TMPRSS15 gene information
    Official name: transmembrane protease, serine 15

    Found related term: ...Life-threatening intestinal malabsorption disorder characterized by diarrhea...
15. SLC10A2 gene information
    Official name: solute carrier family 10 (sodium/bile acid cotransporter family), member 2

    Found related term: Primary bile acid malabsorption (PBAM) [MIM:613291]: An intestinal...
16. SLC5A1 gene summary
    Official name: solute carrier family 5 (sodium/glucose cotransporter), member 1

    Found related term: ...that cause glucose-galactose malabsorption have been identified in the SLC5A1...
17. BAAT gene information
    Official name: bile acid CoA: amino acid N-acyltransferase (glycine N-choloyltransferase)

    Found related term: ...itching, and fat malabsorption. Note=The disease may be caused...
18. TJP2 gene information
    Official name: tight junction protein 2

    Found related term: ...itching, and fat malabsorption. Note=The disease may be caused...
19. COX4I2 gene information
    Official name: cytochrome c oxidase subunit IV isoform 2 (lung)

    Found related term: ...insufficiency, intestinal malabsorption, failure to thrive, and anemia...
20. NEUROG3 gene information
    Official name: neurogenin 3

    Found related term: ...associated with generalized malabsorption and a paucity of enteroendocrine...