Rhizomelic chondrodysplasia punctata type 5

Any rhizomelic chondrodysplasia punctata in which the cause of the disease is a mutation in the PEX5 gene.

Also known as: PEX5 rhizomelic chondrodysplasia punctata, RCDP5, Rcdp5, rhizomelic chondrodysplasia punctata caused by mutation in PEX5, rhizomelic chondrodysplasia punctata type 5, rhizomelic chondrodysplasia punctata, type 5

8 clinical trials for this condition and its sub-types, 1 tagged with Rhizomelic chondrodysplasia punctata type 5 itself.