| Human Disease |
Charcot-Marie-Tooth Disease, X-Linked Recessive, 5; CMTX5 OMIM ID: 311070 |
| Synonyms | Charcot-Marie-Tooth Neuropathy, X-Linked Recessive, 5; Optic Atrophy, Polyneuropathy, and Deafness; Rosenberg-Chutorian Syndrome |
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Genes and mouse models |
There are currently no human or mouse genes associated with this disease in the MGI database. |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/05/2013 MGI 5.13 |
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