You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Congenital microvillous atrophy, look for clinical trials, and connect with others living with it — all in one place.
Open the full Congenital microvillous atrophy hub →Congenital microvillous atrophy is a rare condition. Also known as Congenital microvillous atrophy, Congenital microvillus atrophy, MVID, Microvillous inclusion disease. Tomeko brings together the specialists, research, clinical trials, treatments and community for Congenital microvillous atrophy so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:2290 · OMIM 251850, 619445, 619446 · ICD-10 P78.3 · GARD 0007039
Start by learning the basics from an authoritative source, find a specialist or center that sees Congenital microvillous atrophy, 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 Congenital microvillous atrophy, filtered to your area.
Tomeko shows live, recruiting studies for Congenital microvillous atrophy from ClinicalTrials.gov on the hub.