MeSH Browser

MeSH Supplementary: Chondrodysplasia Punctata with Coagulation Factor Deficiency
Unique ID: C564742
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564742
Registry Numbers: 0
Heading Mapped to: *Chondrodysplasia Punctata; *Coagulation Protein Disorders
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Chondrodysplasia Punctata with Coagulation Factor Deficiency MeSH Supplementary Concept Data 2025