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Disease Ontology Browser
chromosome Xp11.22 duplication syndrome (DOID:0112037)
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Synonyms: MRX17; MRX31; X-linked mental retardation 17; X-linked mental retardation 31; Xp11.22 microduplication syndrome
Alt IDs: OMIM:300705
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.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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12/10/2024
MGI 6.24 		The Jackson Laboratory