Disease #00185 (CMT2A1 (CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1), OMIM:118210)

Official abbreviation CMT2A1
Name CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1
OMIM ID 118210
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene KIF1B
Associated tissues -
Disease features -
Remarks -

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