radiation sensitivity chromosome instability syndrome, autosomal dominant

Preferred Label : radiation sensitivity chromosome instability syndrome, autosomal dominant;

MeSH note : autosomal dominant neurodegenerative disorder with mild chromosome instability and radiation sensitivity, short stature, mental retardation, depression, dysarthria, hyperreflexia, and ataxic gait.;

Details

Origin ID

C565326;

UMLS CUI

C1854244;

MeSH term(s) associated for indexing
- chromosomal instability [MeSH Descriptor]
- neurodegenerative diseases [MeSH Descriptor]
- radiation tolerance [MeSH Descriptor]
Record concept(s)
- radiation sensitivity chromosome instability syndrome, autosomal dominant [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Radiation sensitivity/chromosome instability syndrome, autosomal dominant [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients