Chromosome 17p13.3, centromeric, duplication syndrome

Preferred Label : Chromosome 17p13.3, centromeric, duplication syndrome;

Type : Phenotype, molecular basis known;

Prefixed ID : #613215;

Details

Origin ID

613215;

UMLS CUI

C3808300;

Currated CISMeF NLP mapping
- 17p13.3 duplication [ICD-11 More detail]
- 17p13.3 microduplication syndrome [ORDO Disease]
- 17p13.3 microduplication syndrome (disorder) [SNOMED CT concept]
- chromosome 17p13.3 duplication syndrome [DO Concept]
- chromosome 17p13.3 duplication syndrome [MeSH concept]
- chromosome 17p13.3 duplication syndrome [MeSH Supplementary Concept]
DO Cross reference
- chromosome 17p13.3 duplication syndrome [DO Concept]
ORDO concept(s)
- 17p13.3 microduplication syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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