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Human Disease and Mouse Model Detail
Human Disease

Term: Fountain Syndrome
OMIM ID: 229120

Synonyms Mental Retardation, Sensorineural Deafness, Skeletal Abnormalities, and Coarse Face with Full Lips
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
Funding Information
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Send questions and comments to User Support. 		last database update
04/03/2013
MGI 5.12 		The Jackson Laboratory