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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
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last database update
01/20/2015
MGI 5.21
The Jackson Laboratory