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Disease Ontology Browser
X-linked mental retardation Gustavson type (DOID:0081123)
Alliance: disease page
Synonyms: mental retardation with optic atrophy, deafness and seizures
Alt IDs: OMIM:309555, ORDO:3078
Definition: A syndromic X-linked intellectual disability that is characterized by severe intellectual disability, microcephaly, post-natal growth retardation, severe visual impairment or blindness, severe hearing defect, spasticity, epileptic seizures, restricted large-joint movements and early death.


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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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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory