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Disease Ontology Browser
autosomal dominant intellectual developmental disorder 77 (DOID:0081469)
Alliance: disease page
Alt IDs: OMIM:621415
Definition: An autosomal dominant intellectual developmental disorder that is characterized by global developmental delay that leads to mild to moderate intellectual disability and that has_material_basis_in heterozygous mutation in the LRRC7 gene on chromosome 1q31.1.


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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last database update
07/14/2026
MGI 6.24
The Jackson Laboratory