Charcot-Marie-Tooth disease type 4G

Summary

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

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: hk1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011534 - Charcot-Marie-Tooth disease type 4G

MONDO:0011534 - Charcot-Marie-Tooth disease type 4G

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 type 4 (is_a), autosomal recessive disease (is_a)