MeSH Browser

MeSH Supplementary: Jacobs syndrome
Unique ID: C537560
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537560
Entry Term(s): Arthropathy camptodactyly syndrome; Arthropathy-Camptodactyly Syndrome; Camptodactyly arthropathy pericarditis syndrome; Camptodactyly-Arthropathy-Pericarditis Syndrome; Camptodactyly-arthropathy-coxa vara-pericarditis syndrome; Congenital familial hypertrophic synovitis; Fibrosing serositis, familial; Hypertrophic Synovitis, Congenital Familial; Pericarditis arthropathy camptodactyly syndrome; Pericarditis-Arthropathy-Camptodactyly Syndrome
Registry Numbers: 0
Heading Mapped to: *Arthropathy, Neurogenic; *Hand Deformities, Congenital; *Synovitis; *Coxa Vara
Frequency: 17
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Jacobs syndrome MeSH Supplementary Concept Data 2024