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Human Disease and Mouse Model Detail
Human Disease Choroideremia, Deafness, and Mental Retardation
OMIM ID: 303110
Human Phenotype Ontology associations
Synonyms Chromosome Xq21 Deletion Syndrome
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 6.07
The Jackson Laboratory