About   Help   FAQ
The MGI survey is now closed.
Thanks for your support!
Human Disease and Mouse Model Detail
Human Disease Neuropathy, Hereditary Motor and Sensory, with Excessive Myelin Folding Complex, Autosomal Recessive
OMIM ID: 256855
Synonyms Charcot-Marie-Tooth Disease with Excessive Myelin Folding, Autosomal Recessive; HMSN with Excessive Myelin Outfolding, Autosomal Recessive
Genes and
mouse models
There are currently no human or mouse genes associated with this disease in the MGI database.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
01/20/2015
MGI 5.21
The Jackson Laboratory