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Disease Ontology Browser
chromosome 18p deletion syndrome (DOID:0060406)
Alliance: disease page
Synonyms: 18p- syndrome; De Grouchy syndrome; monosomy 18p
Alt IDs: OMIM:146390, MESH:C538309, NCI:C84521, ORDO:1598, UMLS_CUI:C0432442
Definition: A chromosomal deletion syndrome that has_material_basis_in partial or complete deletion of the short arm of chromosome 18.

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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Send questions and comments to User Support. 		last database update
04/23/2024
MGI 6.23 		The Jackson Laboratory