|OBO ID: DOID:0112037|
|Term Name:||chromosome Xp11.22 duplication syndrome||Search Ontology:|
|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)|
|is a type of:||
OTHER chromosome Xp11.22 duplication syndrome PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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