Tn Syndrome MeSH Supplementary Concept Data 2024

Details
Concepts

MeSH Supplementary: Tn Syndrome
Unique ID: C562719
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562719
Entry Term(s): Galactosyltransferase Deficiency
Heading Mapped to: *Autoimmune Diseases
Frequency: 2
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Tn Syndrome Preferred

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