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Disease Ontology Browser
Charcot-Marie-Tooth disease type 6 (DOID:0080068)
Alliance: disease page
Synonyms: hereditary motor and sensory neuropathy type 6
Alt IDs: OMIM:601152, OMIM:616505
Definition: A Charcot-Marie-Tooth disease that is characterized by early-onset optic atrophy resulting in progressive visual loss and peripheral axonal sensorimotor neuropathy with highly variable age at onset and severity.

Disease References using Mouse Models (1)
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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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory