About   Help   FAQ
Disease Ontology Browser
chromosome 17q23.1-q23.2 deletion syndrome (DOID:0060405)
Alliance: disease page
Synonyms: 17q23.1-q23.2 microdeletion syndrome; 17q23.1q23.2 microdeletion syndrome
Alt IDs: OMIM:613355, ICD10CM:Q93.5, ORDO:261279
Definition: A chromosomal deletion syndrome that has_material_basis_in a chromosome 17q23.1-q23.2 deletion and that is characterized by characterized by developmental delay, microcephaly, short stature, heart defects and limb abnormalities.

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
12/10/2024
MGI 6.24 		The Jackson Laboratory