About   Help   FAQ
Disease Ontology Browser
chromosome 22q11.2 deletion syndrome, distal (DOID:0060413)
Alliance: disease page
Synonyms: DiGeorge syndrome and Velocardiofacial syndrome; distal 22q11.2 microdeletion syndrome
Alt IDs: OMIM:611867, MESH:C567511, ORDO:261330
Definition: A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome 22q11.2 region, distinct from DiGeorge syndrome and velocardiofacial syndrome.

Disease References using Mouse Models (6)
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
10/29/2024
MGI 6.24 		The Jackson Laboratory