MeSH Browser

MeSH Supplementary: Massa Casaer Ceulemans syndrome
Unique ID: C536031
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536031
Entry Term(s): Arthrogryposis multiplex congenita associated with lissencephaly
Registry Numbers: 0
Heading Mapped to: *Arthrogryposis; *Lissencephaly
Frequency: 0
Date of Entry: 2010/08/25
Revision Date: 1955/01/01

Massa Casaer Ceulemans syndrome MeSH Supplementary Concept Data 2025