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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: autosomal dominant axonal Charcot-Marie-Tooth disease type 2L, autosomal dominant Charcot-Marie-Tooth disease type 2L, Charcot-Marie-Tooth neuropathy axonal type 2L, CMT2L
Echinobase Genes
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| MIM:608673 - charcot-marie-tooth disease, axonal, type 2l; cmt2l |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee