Charcot-Marie-Tooth disease dominant intermediate D

Summary

DOID:0110200 - Charcot-Marie-Tooth disease dominant intermediate D

Disease Ontology Definition:A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in heterozygous mutation in the myelin protein-zero gene (MPZ) on chromosome 1q23.

Synonyms: CMTDID, Charcot-Marie-Tooth neuropathy dominant intermediate D, DI-CMTD, autosomal dominant intermediate Charcot-Marie-Tooth disease type D,

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

: mpz

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011909 - Charcot-Marie-Tooth disease dominant intermediate D

MONDO:0011909 - Charcot-Marie-Tooth disease dominant intermediate D

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 intermediate type (is_a), autosomal dominant disease (is_a)