Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Autosomal recessive osteopetrosis · Infantile osteopetrosis with neuroaxonal dysplasia
Autosomal recessive osteopetrosis 5
Any autosomal recessive malignant osteopetrosis in which the cause of the disease is a mutation in the OSTM1 gene.
This condition has no sub-types.