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Lipodystrophy, Congenital Generalized, Type 3 MeSH Supplementary Concept Data 2022


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 Number
0
Heading Mapped to
*Lipodystrophy, Congenital Generalized
Frequency
2
Date of Entry
2012/11/05
Lipodystrophy, Congenital Generalized, Type 3 Preferred
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