Welcome to the international registry of Microvillus Inclusion Disease (MVID) patients and associated MYO5B, STX3 and STXBP2 mutations.

The international Microvillus Inclusion Disease Patient Registry contains anonymised data on both published and unpublished MVID patients, as well as their associated MYO5B, STX3 and STXBP2 mutations and genotypes, and clinical and molecular phenotypes.

The database currently contains 188 MVID patients, and 106 mutations. Search or browse below.

Login to enter data/patients is not yet possible. Please contact Dr IJzendoorn for contributions (s.c.d.van.ijzendoorn@umcg.nl).

Please continue to tab Genes. Your gene of interest can be selected from the menu.