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Chondrodysplasia Punctata, Autosomal Dominant MeSH Supplementary Concept Data 2023


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 Number
0
Heading Mapped to
*Chondrodysplasia Punctata
Frequency
0
Date of Entry
2012/11/05
Chondrodysplasia Punctata, Autosomal Dominant Preferred
Chondrodysplasia Punctata Due To Vitamin K Deficiency Related
Chondrodysplasia Punctata Due To Warfarin Teratogenicity Related
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