chromosome 8q21.11 deletion syndrome Disease Ontology Browser

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Disease Ontology Browser

chromosome 8q21.11 deletion syndrome (DOID:0060425)
Alliance: disease page
Synonyms: 8q21.11 microdeletion syndrome
Alt IDs: OMIM:614230, ICD10CM:Q93.5, ORDO:284160
Definition: A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome 8q21.11 region and that is characterized by intellectual disability and common facial dysmorphic features.

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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