Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Osteogenesis imperfecta and a reduction of bone mineral density. · Singleton-Merten dysplasia · IFIH1-related type 1 interferonopathy
Singleton-Merten syndrome 1
Any singleton-Merten dysplasia in which the cause of the disease is a mutation in the IFIH1 gene.
This condition has no sub-types.