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Human Disease and Mouse Model Detail
Human Disease Fountain Syndrome
OMIM ID: 229120
Human Phenotype Ontology associations
Synonyms Mental Retardation, Sensorineural Deafness, Skeletal Abnormalities, and Coarse Face with Full Lips
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
MGI 6.07
The Jackson Laboratory