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Yu-Kury neurodevelopmental syndrome (DOID:0070695)
Alliance: disease page
Alt IDs: OMIM:621565
Definition: An autosomal dominant intellectual developmental disorder characterized by developmental delay, speech delay, motor delay, and intellectual disability that has_material_basis_in heterozygous mutation in the PSMC5 gene on chromosome 12q23.

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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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04/07/2026
MGI 6.24 		The Jackson Laboratory