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Human Disease and Mouse Model Detail
Human Disease

Term: Gorlin-Chaudhry-Moss Syndrome
OMIM ID: 233500

Synonyms Craniofacial Dysostosis, Hypertrichosis, Hypoplasia of Labia Majora,; Dental and Eye Anomalies, Patent Ductus Arteriosus, and Normal Intelligence; GCM Syndrome
Associated Genes
 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
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Send questions and comments to User Support. 		last database update
04/03/2013
MGI 5.12 		The Jackson Laboratory