About   Help   FAQ
Disease Ontology Browser
chromosome Xp21 deletion syndrome (DOID:0060427)
Alliance: disease page
Synonyms: complex glycerol kinase deficiency; monosomy Xp21; Xp21 microdeletion syndrome
Alt IDs: OMIM:300679, ICD10CM:Q99.8, ORDO:261476

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.12
The Jackson Laboratory