Disease : Rhizomelic chondrodysplasia punctata type 1 (RCDP1 )

Name : Rhizomelic chondrodysplasia punctata type 1 (RCDP1 )
Description : Genetically heterogeneous group of bone dysplasias. Symptoms: disproportionally short stature primally affecting the proximal parts of extremities, typical facial appearance, congenital contractures and severe mental retardation with spasticity.
Gene(s) :
Localization(s) :
  • Cytosol
  • Peroxisome
Functional category(ies) :
Links of Interest: