Poikiloderma, Hereditary Sclerosing MeSH Supplementary Concept Data 2024

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MeSH Supplementary: Poikiloderma, Hereditary Sclerosing
Unique ID: C562824
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562824
Heading Mapped to: *Sclerosis; *Skin Abnormalities; *Skin Diseases, Genetic
Frequency: 9
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Poikiloderma, Hereditary Sclerosing Preferred

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