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Human Disease and Mouse Model Detail
Human Disease Hereditary Motor and Sensory Neuropathy V
OMIM ID: 600361
Synonyms Charcot-Marie-Tooth Disease with Pyramidal Features, Autosomal Dominant; Charcot-Marie-Tooth Neuropathy with Pyramidal Features, Autosomal Dominant; CMT with Pyramidal Features; HMSN5; HMSN V; Peroneal Muscular Atrophy with Pyramidal Features, Autosomal Dominant
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
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Send questions and comments to User Support. 		last database update
05/08/2013
MGI 5.13 		The Jackson Laboratory