MeSH Browser

MeSH Supplementary: Chondrodysplasia Punctata, Autosomal Dominant
Unique ID: C563248
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563248
Entry Term(s): Chondrodysplasia Punctata Due To Vitamin K Deficiency; Chondrodysplasia Punctata Due To Warfarin Teratogenicity
Registry Numbers: 0
Heading Mapped to: *Chondrodysplasia Punctata
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Chondrodysplasia Punctata, Autosomal Dominant MeSH Supplementary Concept Data 2025