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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

Referenced OMIM:

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

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

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

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Version: 4.15.0
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