MeSH Browser

MeSH Supplementary: Distal arthrogryposis type 2B
Unique ID: C538400
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538400
Entry Term(s): Arthrogryposis Multiplex Congenita, Distal, Type II, with Craniofacial Abnormalities; Arthrogryposis multiplex congenita type 2B; Arthrogryposis multiplex congenita, distal, type 2b; Arthrogryposis, distal, type 2b; Freeman-Sheldon Syndrome Variant; Sheldon-Hall syndrome
Registry Numbers: 0
Heading Mapped to: *Arthrogryposis
Frequency: 14
Date of Entry: 2010/11/13
Revision Date: 2012/08/24

Distal arthrogryposis type 2B MeSH Supplementary Concept Data 2025