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Human Disease and Mouse Model Detail
Human Disease Neuropathy, Hereditary Motor and Sensory, Type Via; HMSN6A
OMIM ID: 601152
Human Phenotype Ontology associations
Synonyms Charcot-Marie-Tooth Disease, Type 6; CMT6; Charcot-Marie-Tooth Disease, Type 6a; CMT6A; Hmsn Via; Neuropathy, Hereditary Motor and Sensory; Neuropathy, Hereditary Motor and Sensory, Type VI; HMSN6; Peripheral Neuropathy and Optic Atrophy
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     MFN2* Mfn2   HomoloGene and HGNC

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.07
The Jackson Laboratory