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Summary Literature (0)
DOID:0050540 - Charcot-Marie-Tooth disease type 3

Disease Ontology Definition:A Charcot-Marie-Tooth disease that is characterized by motor and sensory peripheral neuropathies caused by demyelination.

Synonyms: DEJERINE-SOTTAS NEUROPATHY, DEJERINE-SOTTAS SYNDROME

Xenbase Genes : egr2, mpz, pmp22, prx

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007790 - Charcot-Marie-Tooth disease type 3

MIM:
MIM:145900 - HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS

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

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