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DOID:0050539 - Charcot-Marie-Tooth disease type 2
Disease Ontology Definition:A Charcot-Marie-Tooth disease characterized by abnormalities in the axon of the peripheral nerve cell.
Synonyms: hereditary motor and sensory neuropathy Guadalajara neuronal type, hereditary motor and sensory neuropathy Okinawa type, hereditary motor and sensory neuropathy type 2,
Echinobase Genes : lrsam1, dhtkd1, dync1h1, rab7a, pnkp, aars1
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
Charcot-Marie-Tooth disease (is_a)