Diseases Studied
The Rare Diseases Clinical Research Network is an NIH-funded research network of 20 active consortia or research groups working to advance treatment for diseases that are rare. Use the search tools on this page to find the diseases we currently study. You can reach out to the indicated consortia or research groups for more information on those diseases and studies underway.
This network focuses on clinical research and does not generally support clinical care outside of research activities. To learn about other rare diseases, please visit the Genetic and Rare Diseases Information Center (GARD), which is an NIH program that helps the public find reliable information about rare and genetic diseases. Their staff are specialists. Contact them at 1-888-205-2311 or email GARDinfo@nih.gov.
All Diseases > MOGS-congenital disorder of glycosylation
MOGS-congenital disorder of glycosylation
Alternative Names: MOGS-CDG
Disease Category: Congenital Disorders of Glycosylation
MOGS-CDG is an ultra-rare inherited condition affecting a specific type of glycosylation, called N-linked glycosylation. Symptoms often include generalized hypotonia, developmental delays, less developed genitalia, seizures, feeding difficulties, shallow breathing, distinct facial features, and hypogammaglobulinemia.
Research groups studying this disease
Congenital Disorders of Glycosylation
Frontiers in Congenital Disorders of Glycosylation (FCDGC)