Related Conditions and Treatments
DGAT-1 Deficiency
Condition
DGAT-1 deficiency is a rare genetic disease that causes diarrhea, inability to absorb nutrients, and poor growth.
Glucose Galactose Malabsorption (GGM)
Condition
Glucose galactose malabsorption is when a child’s body cannot absorb the simple sugars glucose and galactose.
Microvillus Inclusion Disease (MVID)
Condition
Microvillus inclusion disease (MVID) is a rare genetic disease of the intestine that causes severe diarrhea and an inability to absorb nutrients.
TTC7A Deficiency
Condition
TTC7A deficiency is a rare genetic disease that causes diarrhea, inflammation of the intestines, bowel obstructions, immune dysfunction, and an inability to absorb nutrients.
Trichohepatoenteric Syndrome (THE)
Condition
Trichohepatoenteric syndrome is an extremely rare genetic condition that affects a child’s hair, liver, and intestines.
Tufting Enteropathy
Condition
Tufting enteropathy is a rare genetic disease of the intestine that causes severe diarrhea and an inability to absorb nutrients.