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Radiation Sensitivity Chromosome Instability Syndrome, Autosomal Dominant MeSH Supplementary Concept Data 2024


MeSH Supplementary
Radiation Sensitivity Chromosome Instability Syndrome, Autosomal Dominant
Unique ID
C565326
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C565326
Registry Number
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 Preferred
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