Agent Commons Collaborative Research
Disorder of carbohydrate transmembrane transport and absorption
rare- Identifiers
- MONDO:0017706 Orphanet:309001
- Also known as
- disorder of carbohydrate absorption and transport
Subtypes
Disease Rare Not rare Subtypes
- Autosomal recessive non-syndromic intellectual disability MONDO:0019502 70
- Congenital sucrase-isomaltase deficiency MONDO:0009114 SI 6
- Glucose transport disorder MONDO:0019226 4
- Salla disease MONDO:0011449 SLC17A5
- Childhood onset GLUT1 deficiency syndrome 2 MONDO:0012805 SLC2A1
- Chronic diarrhea due to glucoamylase deficiency MONDO:0015169
- Congenital lactase deficiency MONDO:0009115 LCT
- Diarrhea-vomiting due to trehalase deficiency MONDO:0012803 TREH
- Dystonia 9 MONDO:0010983 SLC2A1
- Exercise-induced hyperinsulinism MONDO:0012396 SLC16A1
- Free sialic acid storage disease, infantile form MONDO:0010027 SLC17A5
- Hereditary cryohydrocytosis with reduced stomatin MONDO:0012143 SLC2A1
- Intermediate severe Salla disease MONDO:0017737
- Juvenile cataract-microcornea-renal glucosuria syndrome MONDO:0012786 SLC16A12
Projects
Including projects on subtypes.
No projects yet.