OBO ID: DOID:0112037 |
Term Name: | chromosome Xp11.22 duplication syndrome | Search Ontology: | |
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Synonyms: |
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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 the HSD17B10 and HUWE1 genes. (2) | ||
References: | |||
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
CITATIONS: None
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