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Summary Literature (0)
DOID:0080067 - Charcot-Marie-Tooth disease type 5


Disease Ontology Definition:A Charcot-Marie-Tooth disease that is characterized by pyramidal features including extensor plantar responses, mild increase in tone, and preserved or increased reflexes but no spastic gait.

Synonyms: hereditary motor and sensory neuropathy with pyramidal features


In Mondo Disease Ontology:
MONDO:0010877 - Charcot-Marie-Tooth disease type 5

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : mfn2

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): Charcot-Marie-Tooth disease (is_a)