Disease #06538 (CMT2CC (Charcot-Marie-Tooth disease, axonal, type 2CC), OMIM:616924)

Official abbreviation CMT2CC
Name Charcot-Marie-Tooth disease, axonal, type 2CC
OMIM ID 616924
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 NEFH
Associated tissues -
Disease features -
Remarks -

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