MeSH Browser

MeSH Supplementary: Boylan Dew Greco syndrome
Unique ID: C537083
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537083
Entry Term(s): Congenital hypomyelination neuropathy with arthrogryposis multiplex congenita
Registry Number: 0
Heading Mapped to: *Arthrogryposis; *Demyelinating Diseases
Frequency: 0
Date of Entry: 2010/08/25

Boylan Dew Greco syndrome MeSH Supplementary Concept Data 2023