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Disease Ontology Browser
Waisman syndrome (DOID:0111781)
Alliance: disease page
Synonyms: early-onset parkinsonism-intellectual disability syndrome; Laxova-Opitz syndrome
Alt IDs: OMIM:311510
Definition: A syndrome characterized by delayed psychomotor development, impaired intellectual development, and early-onset Parkinson disease that has_material_basis_in hemizygous or homozygous mutation in the RAB39B gene on chromosome Xq28.

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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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory