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Disease Ontology Browser
chromosome 14q11-q22 deletion syndrome (DOID:0060392)
Alliance: disease page
Synonyms: 14q11.2 microdeletion syndrome
Alt IDs: OMIM:613457, ORDO:261120
Definition: A chromosomal deletion syndrome that is characterized by microcephaly, dysmorphic facies, psychomotor delay and failure to thrive, has_material_basis_in isolated cases of partial deletion of the long arm of chromosome 14.

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
12/10/2024
MGI 6.24 		The Jackson Laboratory