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Human Disease and Mouse Model Detail
Human Disease Behr Syndrome; BEHRS
OMIM ID: 210000
Synonyms Optic Atrophy, Infantile Hereditary, with Neurologic Abnormalities
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
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last database update
MGI 6.04
The Jackson Laboratory