chromosome 18q deletion syndrome Disease Ontology Browser

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Disease Ontology Browser

chromosome 18q deletion syndrome (DOID:0060407)
Alliance: disease page
Synonyms: 18q- syndrome; deletion 18q; monosomy 18q
Alt IDs: OMIM:601808, ICD10CM:Q93.5, MESH:C536580, ORDO:1600
Definition: A chromosomal deletion syndrome that has_material_basis_in a terminal deficiency or macrodeletion that is characterized by mental retardation and congenital malformations.

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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