OBO ID: DOID:0112037
Term Name: chromosome Xp11.22 duplication syndrome Search Ontology:
  • MRX17
  • MRX31
  • X-linked mental retardation 17
  • X-linked mental retardation 31
  • Xp11.22 microduplication syndrome
Definition: A non-syndromic X-linked intellectual disability characterized by moderate intellectual disability and slow speech development that has_material_basis_in duplication of a small region within chromosome Xp11.22 involving both HSD17B10 and HUWE1. (2)
Ontology: Human Disease   (DOID:0112037)
OTHER chromosome Xp11.22 duplication syndrome PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available