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Summary Literature (1)
DOID:0050538 - Charcot-Marie-Tooth disease type 1

Disease Ontology Definition:A Charcot-Marie-Tooth disease characterized by demyelination of the peripheral nerve axons.

Synonyms: hereditary motor and sensory neuropathy type 1,

Xenbase Genes : nefl, egr2, mpz, pmp22, litaf

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0019011 - Charcot-Marie-Tooth disease type 1


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): Charcot-Marie-Tooth disease (is_a)