/autosomal dominant chondrodysplasia punctata

autosomal dominant chondrodysplasia punctata

Rare Disease

MONDO:0007321

Also Known As

chondrodysplasia punctata Sheffield typechondrodysplasia punctata, Sheffield typechondrodysplasia punctata, autosomal dominantchondrodysplasia punctata due to vitamin K deficiencychondrodysplasia punctata due to warfarin teratogenicity

Definition

Autosomal dominant form of chondrodysplasia punctata.

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autosomal dominant chondrodysplasia punctata

Also Known As

Definition

Patient-Friendly Information

External Resources

OMIM

Orphanet

GARD

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