You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Tryptophan malabsorption syndrome, look for clinical trials, and connect with others living with it — all in one place.
Open the full Tryptophan malabsorption syndrome hub →Tryptophan malabsorption syndrome is a rare condition. Also known as Drummond syndrome, Familial hypercalcemia-nephrocalcinosis-indicanuria syndrome. Tomeko brings together the specialists, research, clinical trials, treatments and community for Tryptophan malabsorption syndrome so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:94086 · OMIM 211000 · ICD-10 E70.8 · GARD 0005939
Start by learning the basics from an authoritative source, find a specialist or center that sees Tryptophan malabsorption syndrome, and connect with a patient organization. Tomeko brings these together on one hub.
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Tryptophan malabsorption syndrome, filtered to your area.
Tomeko shows live, recruiting studies for Tryptophan malabsorption syndrome from ClinicalTrials.gov on the hub.