Dyskeratosis Congenita, Autosomal Dominant MeSH Supplementary Concept Data 2023

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Concepts

MeSH Supplementary: Dyskeratosis Congenita, Autosomal Dominant
Unique ID: C565079
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565079
Entry Term(s): Dyskeratosis Congenita, Scoggins Type
Registry Number: 0
Heading Mapped to: *Dyskeratosis Congenita
Frequency: 5
Date of Entry: 2012/11/05

Dyskeratosis Congenita, Autosomal Dominant Preferred

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