Charcot-Marie-Tooth disease dominant intermediate B

Summary

DOID:0110197 - Charcot-Marie-Tooth disease dominant intermediate B

Disease Ontology Definition:A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in mutation in the gene encoding dynamin-2 (DNM2).

Synonyms: Charcot-Marie-Tooth neuropathy dominant intermediate B, CMTDI1, CMTDIB, DI-CMTB

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

: dnm2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011674 - Charcot-Marie-Tooth disease dominant intermediate B

MONDO:0011674 - Charcot-Marie-Tooth disease dominant intermediate B

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), Charcot-Marie-Tooth disease intermediate type (is_a)