. _:vb50945050 . "A Charcot-Marie-Tooth disease type 2 characterized by onset of peripheral neuropathy in the first years of life that has_material_basis_in homozygous or compound heterozygous mutation in MFN2 on chromosome 1p36.22."^^ . _:vb50945050 . . "Charcot-Marie-Tooth disease type 2A2B"^^ . . "OMIM:617087"^^ . _:vb50945050 . "autosomal recessive Charcot-Marie-Tooth disease, Ouvrier type"@en . _:vb50945050 . _:vb50945050 . "CMT2A2B"@en . "severe early-onset axonal neuropathy due to MFN2 deficiency"@en . "Charcot-Marie-Tooth disease, axonal, type 2A2B"@en . "SEOAN due to MFN2 deficiency"@en . "disease_ontology"^^ . . "DOID:0111557"^^ . "ORDO:90118"^^ . "AR-CMT2, Ouvrier type"@en .