MeSH Browser

MeSH Supplementary: Arthrogryposis multiplex congenita, distal, X-linked
Unique ID: C535380
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535380
Entry Term(s): AMC, distal, X-linked; Amcx1; Arthrogryposis, X-Linked, Type I; Smax2; Spinal Muscular Atrophy, Infantile X-Linked; Spinal Muscular Atrophy, X-Linked 2; Spinal Muscular Atrophy, X-Linked Lethal Infantile; Xlsma
Registry Number: 0
Heading Mapped to: *Arthrogryposis; *Genetic Diseases, X-Linked
Frequency: 3
Date of Entry: 2010/08/25
Revision Date: 2012/08/24

Arthrogryposis multiplex congenita, distal, X-linked MeSH Supplementary Concept Data 2024