Autosomal dominant chondrodysplasia punctata

MONDO:0007321

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

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