non-syndromic X-linked intellectual disability 101 Disease Ontology Browser

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Disease Ontology Browser

non-syndromic X-linked intellectual disability 101 (DOID:0112048)
Alliance: disease page
Synonyms: MRX101; X-linked mental retardation 101
Alt IDs: OMIM:300928
Definition: A non-syndromic X-linked intellectual disability characterized by global developmental delay that has_material_basis_in hemizygous mutation in the MID2 gene on chromosome Xq22.3.

Contributing Projects: 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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