MeSH Browser

MeSH Supplementary: Cerebrooculofacioskeletal Syndrome 2
Unique ID: C565185
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565185
Registry Numbers: 0
Heading Mapped to: *Arthrogryposis; Cataract / congenital; *Intellectual Disability; *Craniofacial Abnormalities
Frequency: 0
Note: mutation in ERCC2 (XPD)
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Cerebrooculofacioskeletal Syndrome 2 MeSH Supplementary Concept Data 2025