About   Help   FAQ
Disease Ontology Browser
distal 10q deletion syndrome (DOID:0060390)
Alliance: disease page
Synonyms: chromosome 10q26 deletion syndrome; distal monosomy 10q; monosomy 10qter; telomeric deletion 10q; terminal chromosome 10q26 deletion syndrome
Alt IDs: OMIM:609625, ICD10CM:Q93.5, MESH:C567182, ORDO:96148
Definition: A chromosomal deletion syndrome that is characterized by developmental delay, intellectual disability, behavioral problems and facial facies caused by a missing copy of the long arm of chromosome 10.

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