MeSH Browser

MeSH Supplementary: Radiation Sensitivity Chromosome Instability Syndrome, Autosomal Dominant
Unique ID: C565326
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565326
Registry Numbers: 0
Heading Mapped to: Radiation Tolerance; Neurodegenerative Diseases / congenital; *Chromosomal Instability
Frequency: 0
Note: autosomal dominant neurodegenerative disorder with mild chromosome instability and radiation sensitivity, short stature, mental retardation, depression, dysarthria, hyperreflexia, and ataxic gait.
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Radiation Sensitivity Chromosome Instability Syndrome, Autosomal Dominant MeSH Supplementary Concept Data 2025