MeSH Browser

MeSH Supplementary: Multiple Pterygium Syndrome, Autosomal Dominant
Unique ID: C566739
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566739
Entry Term(s): Arthrogryposis, Distal, Type 8; Pterygium Syndrome, Multiple, Autosomal Dominant
Heading Mapped to: *Arthrogryposis
Frequency: 57
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Multiple Pterygium Syndrome, Autosomal Dominant MeSH Supplementary Concept Data 2024