About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease Pierre Robin Sequence with Pectus Excavatum and Rib and Scapular Anomalies
OMIM ID: 602196
Synonyms Campomelic Dysplasia, Mild; Skeletal Dysplasia Related to Campomelic Dysplasia
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
05/08/2013
MGI 5.13 		The Jackson Laboratory