Spondyloepiphyseal Dysplasia Tarda, Autosomal Dominant MeSH Supplementary Concept Data 2025

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Concepts

MeSH Supplementary: Spondyloepiphyseal Dysplasia Tarda, Autosomal Dominant
Unique ID: C566658
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566658
Registry Numbers: 0
Heading Mapped to: *Osteochondrodysplasias
Frequency: 1
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Spondyloepiphyseal Dysplasia Tarda, Autosomal Dominant Preferred

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