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Disease Ontology Browser
Charcot-Marie-Tooth disease type 2 (DOID:0050539)
Alliance: disease page
Synonyms: hereditary motor and sensory neuropathy Guadalajara neuronal type; hereditary motor and sensory neuropathy Okinawa type; hereditary motor and sensory neuropathy type 2
Alt IDs: OMIM:118230, OMIM:604484, ICD9CM:356.0, ORDO:64746, UMLS_CUI:C0392553
Definition: A Charcot-Marie-Tooth disease characterized by abnormalities in the axon of the peripheral nerve cell.

Disease References using Mouse Models (28)
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
12/10/2024
MGI 6.24 		The Jackson Laboratory