Sclerocornea, Autosomal Dominant MeSH Supplementary Concept Data 2024

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Concepts

MeSH Supplementary: Sclerocornea, Autosomal Dominant
Unique ID: C566692
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566692
Registry Number: 0
Heading Mapped to: *Corneal Diseases; Sclera / *abnormalities
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Sclerocornea, Autosomal Dominant Preferred

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