Autosomal dominant chondrodysplasia punctata

Autosomal dominant form of chondrodysplasia punctata.

Also known as: chondrodysplasia punctata Sheffield type, chondrodysplasia punctata, Sheffield type, chondrodysplasia punctata, autosomal dominant, chondrodysplasia punctata due to vitamin K deficiency, chondrodysplasia punctata due to warfarin teratogenicity

35 clinical trials for this condition and its sub-types.