MeSH Browser

MeSH Supplementary: Gordon syndrome
Unique ID: C537288
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537288
Entry Term(s): Arthrogryposis Multiplex Congenita, Distal, Type IIa; Arthrogryposis multiplex congenita, distal, type 2a; Arthrogryposis, distal, type 3; Camptodactyly, cleft palate, and clubfoot; Distal arthrogryposis, type 3
Registry Number: 0
Heading Mapped to: *Arthrogryposis; *Cleft Palate; *Clubfoot; *Hand Deformities, Congenital
Frequency: 20
Date of Entry: 2010/08/25
Revision Date: 2012/08/24

Gordon syndrome MeSH Supplementary Concept Data 2024