chromosomal instability with Tissue-Specific radiosensitivity

Preferred Label : chromosomal instability with Tissue-Specific radiosensitivity;

Origin ID

C565848;

UMLS CUI

C1859091;

Currated CISMeF NLP mapping
- Chromosomal instability with tissue-specific radiosensitivity [OMIM Phenotype]
MeSH term(s) associated for indexing
- chromosomal instability [MeSH Descriptor]
- microcephaly [MeSH Descriptor]
- neoplasms [MeSH Descriptor]
- neoplasms [MeSH Descriptor]
Record concept(s)
- chromosomal instability with Tissue-Specific radiosensitivity [MeSH concept]
Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
UMLS correspondences (same concept)
- Chromosomal instability with tissue-specific radiosensitivity [OMIM Phenotype]