Atrophia Maculosa Varioliformis Cutis, Familial MeSH Supplementary Concept Data 2024

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MeSH Supplementary: Atrophia Maculosa Varioliformis Cutis, Familial
Unique ID: C563349
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563349
Entry Term(s): Varioliform Macular Atrophy of the Skin
Registry Number: 0
Heading Mapped to: *Skin Diseases, Genetic
Frequency: 1
Date of Entry: 2012/11/05

Atrophia Maculosa Varioliformis Cutis, Familial Preferred

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