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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:0007790 - Charcot-Marie-Tooth disease type 3 |
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),
autosomal dominant disease (is_a),
autosomal recessive disease (is_a)