Dyskeratosis, Hereditary Benign Intraepithelial MeSH Supplementary Concept Data 2025

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Concepts

MeSH Supplementary: Dyskeratosis, Hereditary Benign Intraepithelial
Unique ID: C562551
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562551
Registry Numbers: 0
Heading Mapped to: Epithelium / abnormalities; *Skin Abnormalities
Frequency: 5
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Dyskeratosis, Hereditary Benign Intraepithelial Preferred

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