bn:17887908n
Noun Concept
EN
autosomal dominant chondrodysplasia punctata  chondrodysplasia punctata, autosomal dominant  Chondrodysplasia punctata, Sheffield type  Chondrodysplasia Punctata Due to Vitamin K Deficiency  Chondrodysplasia Punctata Due to Warfarin Teratogenicity
EN
Human disease Wikidata
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