Charcot-Marie-Tooth disease type 4F

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Summary

Literature (0)

DOID:0110193 - Charcot-Marie-Tooth disease type 4F

Disease Ontology Definition:A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous or compound heterozygous mutation in the periaxin gene (PRX) on chromosome 19q13.

Synonyms: CMT4F

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

: prx

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013959 - Charcot-Marie-Tooth disease type 4F

MONDO:0013959 - Charcot-Marie-Tooth disease type 4F

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

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

Parent(s): autosomal recessive disease (is_a), Charcot-Marie-Tooth disease type 4 (is_a)