Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Echinobase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Echinobase
Summary Literature (0)
DOID:0110174 - Charcot-Marie-Tooth disease axonal type 2L


Disease Ontology Definition:A Charcot-Marie-Tooth disease type 2 that has_material_basis_in mutation in the HSPB8 gene.

Synonyms: CMT2L, Charcot-Marie-Tooth neuropathy axonal type 2L, autosomal dominant Charcot-Marie-Tooth disease type 2L, autosomal dominant axonal Charcot-Marie-Tooth disease type 2L,

Echinobase Genes :


OMIM:
MIM:608673 - charcot-marie-tooth disease, axonal, type 2l; cmt2l

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 2 (is_a)