Disease #03301 (CMT2N (Charcot-Marie-Tooth disease, type 2N (CMT2N)), OMIM:613287)

Official abbreviation CMT2N
Name Charcot-Marie-Tooth disease, type 2N (CMT2N)
OMIM ID 613287
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene AARS
Associated tissues -
Disease features -
Remarks -