Search Ontology:
Human Disease

chromosome 17p13.3 duplication syndrome

Term ID
DOID:0060432
Synonyms
  • 17p13.3 duplication syndrome
  • 17p13.3 microduplication syndrome
  • chromosome 17p13.3 centromeric duplication syndrome
  • trisomy 17p13.3
Definition
A chromosomal duplication syndrome that has_material_basis_in the PAFAH1B1 and/or the YWHAE gene on chromosome 17p13.3. https://pubmed.ncbi.nlm.nih.gov/19136950/
References
Ontology
Human Disease   ( DOID:0060432 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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