appears_in: []
contributor:
  email: cthoyt@gmail.com
  github: cthoyt
  name: Charles Tapley Hoyt
  orcid: 0000-0003-4423-4370
depends_on: []
deprecated: false
description: CNV syndromes in the DECIPHER genomics database that are linked to Human
  Phenotype Ontology terms
example: '1'
homepage: https://www.deciphergenomics.org/
keywords:
- biomedical science
- life science
mappings:
  biocontext: DECIPHER
  fairsharing: FAIRsharing.l8Sf5x
name: DECIPHER CNV Syndromes
pattern: ^\d+$
preferred_prefix: decipher
prefix: decipher
providers: []
publications:
- doi: 10.1093/nar/gkt937
  pmc: PMC3965078
  pubmed: '24150940'
  title: 'DECIPHER: database for the interpretation of phenotype-linked plausibly
    pathogenic sequence and copy-number variation'
  year: 2013
- doi: 10.1016/j.ajhg.2009.03.010
  pmc: PMC2667985
  pubmed: '19344873'
  title: 'DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using
    Ensembl Resources'
  year: 2009
synonyms: []
uri_format: https://www.deciphergenomics.org/syndrome/$1
