Perrault syndrome 2 Disease Ontology Browser

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Perrault syndrome 2 (DOID:0061117)
Alliance: disease page
Alt IDs: OMIM:614926
Definition: A Perrault syndrome that is characterized by sensorineural deafness in both males and females that has_material_basis_in compound heterozygous mutation in the HARS2 gene on chromosome 5q31.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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