Hyperpigmentation, Familial Progressive MeSH Supplementary Concept Data 2025

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Concepts

MeSH Supplementary: Hyperpigmentation, Familial Progressive
Unique ID: C564163
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564163
Entry Term(s): Melanosis Universalis Hereditaria
Registry Numbers: 0
Heading Mapped to: *Hyperpigmentation
Frequency: 7
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Hyperpigmentation, Familial Progressive Preferred

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