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Summary Literature (0)
DOID:0050541 - Charcot-Marie-Tooth disease type 4

Disease Ontology Definition:A Charcot-Marie-Tooth disease characterized by demyelinating or axonal abnormalities that has_material_basis_in autosomal recessive inheritance.

Synonyms: hereditary motor and sensory neuropathy,

Xenbase Genes : sh3tc2, fgd4, egr2, mpz, hk1, gdap1, ndrg1, sbf2, prx, sbf1, mtmr2, fig4, surf1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0018995 - Charcot-Marie-Tooth disease type 4


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)