chromosome aberrations

Preferred Label : chromosome aberrations;

UMLS semantic type : T049 - Cell or Molecular Dysfunction;

Origin ID

M0004406;

UMLS CUI

C0008625;

Currated CISMeF NLP mapping
- CHROMOSOME ABNORMALITY [WHO-ART Included Term]
- CHROMOSOME DISORDER [WHO-ART High Level Term]
- Chromosomal aberration [PASCAL descriptor]
- Chromosomal abnormality NOS [MedDRA LLT]
- Chromosomal abnormality, unspecified [ICD-10 Sub-category (who)]
- Chromosomal abnormality, unspecified [ICD-10 Sub-category]
- Chromosomal anomalies [MedDRA LLT]
- Chromosomal disorder (disorder) [SNOMED CT concept]
- Chromosome Disorder [NCIt concept]
- Chromosome abnormality [MedDRA LLT]
- Chromosome disorder [MedDRA LLT]
- Conditions due to anomaly of unspecified chromosome [ICD-9 code]
- Congenital disorder due to abnormality of chromosome number OR structure (disorder) [SNOMED CT concept]
- Cytogenetic Abnormality [NCIt concept]
- Cytogenetic abnormality [MedDRA Preferred Term]
- Rare chromosomal anomaly [ORDO Disease]
- chromosomal disease, nos [TUV Term]
- chromosomal disease, nos [SNOMED Notion]
- chromosome aberration [Disease (Nov.)]
- chromosome disorder [Disease (Nov.)]
MeSH narrower concept(s)
- autosome abnormalities [MeSH concept]
Related record
- chromosome aberrations [MeSH Descriptor]
Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
UMLS correspondences (same concept)
- Cytogenetic Abnormality [NCIt concept]
- chromosomal disease, nos [TUV Term]