Welcome to Genetic Disease and Rare Disease database.

GDRD database focuses on human genetic data and phenotype data. Collecting family information, genetic variant and causing mutation from publications and collaborators all over the world. Accelerate data sharing, exchange, and cooperation in the field of genetic diseases and rare diseases. You can search variant, family, and publication by just enter gene, disease, phenotype, genome region and so on.

Example: GJB2 (gene), NM_032709.2 (tanscript), 20:2381081:A:G (variant), 268000 (OMIM ID), 10:12136140-18177428 (region), HP:0000510 (HPO ID).