Term Name: | autosomal dominant intellectual developmental disorder type FRA12A |
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Synonyms: | |
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. |
Ontology: | Human Disease [DOID:0061049] ( DOID:0061049 ) |