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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: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)