duplication 15q11-q13 syndrome

Preferred Label : duplication 15q11-q13 syndrome;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0577905;

UMLS CUI

C2675336;

Currated CISMeF NLP mapping
- 15q11q13 duplication [ICD-11 More detail]
- 15q11q13 microduplication syndrome [ORDO Disease]
- 15q11q13 microduplication syndrome (disorder) [SNOMED CT concept]
- Chromosome 15q11-q13 Duplication Syndrome [NCIt concept]
- Chromosome 15q11-q13 duplication syndrome [OMIM Phenotype]
Related MeSH concept(s)
- microdeletion 15q11.2 [MeSH concept]
Related record
- duplication 15q11-q13 syndrome [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- 15q11q13 microduplication syndrome [ORDO Disease]
- 15q11q13 microduplication syndrome (disorder) [SNOMED CT concept]
- Chromosome 15q11-q13 Duplication Syndrome [NCIt concept]
- Chromosome 15q11-q13 duplication syndrome [OMIM Phenotype]