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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: Charcot-Marie-Tooth disease type 2P, Charcot-Marie-Tooth neuropathy type 2P, CMT2P
Echinobase Genes
:
lrsam1
| MIM:614436 - charcot-marie-tooth disease, axonal, type 2p; cmt2p |
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),
autosomal recessive disease (is_a),
Charcot-Marie-Tooth disease type 2 (is_a)