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Summary Literature (0)
DOID:0110196 - Charcot-Marie-Tooth disease type 4G

Disease Ontology Definition:A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous mutation in the HK1 gene on chromosome 10q22.

Synonyms: autosomal recessive Charcot-Marie-Tooth disease type 4G, Charcot-Marie-Tooth neuropathy type 4G, CMT4G, hereditary motor and sensory neuropathy Russe type, HMSNR

Xenbase Genes : hk1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011534 - Charcot-Marie-Tooth disease type 4G


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), Charcot-Marie-Tooth disease type 4 (is_a)