autosomal dominant intellectual developmental disorder type FRA12A Disease Ontology Browser

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Disease Ontology Browser

autosomal dominant intellectual developmental disorder type FRA12A (DOID:0061049)
Alliance: disease page
Alt IDs: OMIM:136630
Definition: An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous expanded CGG repeat in the 5-prime untranslated region of the DIP2B gene on chromosome 12q13.

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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