Charcot-Marie-Tooth disease axonal type 2P

Summary

DOID:0110169 - Charcot-Marie-Tooth disease axonal type 2P

Disease Ontology Definition:A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous or heterozygous mutation in the LRSAM1 gene on chromosome 9q33.

Synonyms: CMT2P, Charcot-Marie-Tooth disease type 2P, Charcot-Marie-Tooth neuropathy type 2P,

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

: lrsam1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013753 - Charcot-Marie-Tooth disease axonal type 2P

MONDO:0013753 - Charcot-Marie-Tooth disease axonal type 2P

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), autosomal dominant disease (is_a), autosomal recessive disease (is_a)