Ring Chromosome 13 Syndrome

Preferred Label : Ring Chromosome 13 Syndrome;

NCIt definition : A rare condition in which the two arms of chromosome 13 are fused resulting in a ring chromosome. Ring chromosome syndromes typically are characterized by developmental delay, intellectual disability, microcephaly, and dysmorphic facial features.;

NCI Metathesaurus CUI : CL540813;

Détails

Origin ID

C179703;

UMLS CUI

C0795847;

Currated CISMeF NLP mapping
- Ring chromosome 13 syndrome [ORDO Disease]
- Ring chromosome 13 syndrome (disorder) [SNOMED CT concept]
See also inter- (CISMeF)
- chromosome 13 ring [MeSH Supplementary Concept]
- chromosome 13 ring [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Ring chromosome 13 syndrome (disorder) [SNOMED CT concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
disease_mapped_to_chromosome
- Human Chromosome 13 [NCIt concept]

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

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