Chromosomal anomalies

Preferred Label : Chromosomal anomalies;

Inclusion : Syndromes associated with anomalies in the number and form of chromosomes;

Additional codes : Use additional codes for conditions associated with the chromosomal anomalies;

Détails

Origin ID

758;

UMLS CUI

C0008626;

Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- CHROMOSOME ABNORMALITY [WHO-ART Included Term]
- CHROMOSOME DISORDER [WHO-ART High Level Term]
- Chromosomal abnormality NOS [MedDRA LLT]
- 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 [MedDRA LLT]
- Congenital disorder due to abnormality of chromosome number OR structure (disorder) [SNOMED CT concept]
- Cytogenetic abnormality [MedDRA Preferred Term]
- autosomal disorder [Disease (Nov.)]
- chromosomal disease, nos [SNOMED Notion]
- chromosome disorders [MeSH concept]
- chromosome disorders [MeSH Descriptor]

Position du mot-clé dans l'(les) arborescence(s) :

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