About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease Chromosome Xp11.3 Deletion Syndrome
OMIM ID: 300578
Synonyms Chromosome Deletion Syndrome; Mental Retardation, X-Linked, with Retinitis Pigmentosa
Genes and
mouse models
There are currently no human or mouse genes associated with this disease in the MGI database.

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
10/08/2014
MGI 5.20
The Jackson Laboratory