MeSH Browser

MeSH Supplementary: Lipodystrophy, Congenital Generalized, Type 3
Unique ID: C567282
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567282
Entry Term(s): Berardinelli-Seip Congenital Lipodystrophy, Type 3; Bscl3; Cgl3; Lipodystrophy, Berardinelli-Seip Congenital, Type 3
Registry Numbers: 0
Heading Mapped to: *Lipodystrophy, Congenital Generalized
Frequency: 2
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Lipodystrophy, Congenital Generalized, Type 3 MeSH Supplementary Concept Data 2025