Telangiectasia, Hereditary Benign MeSH Supplementary Concept Data 2024

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Concepts

MeSH Supplementary: Telangiectasia, Hereditary Benign
Unique ID: C562908
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562908
Registry Number: 0
Heading Mapped to: Telangiectasis / *congenital
Frequency: 6
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Telangiectasia, Hereditary Benign Preferred

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