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Human Disease and Mouse Model Detail
Human Disease Charcot-Marie-Tooth Disease, Demyelinating, Type 1B; CMT1B
OMIM ID: 118200
Synonyms Charcot-Marie-Tooth Disease, Autosomal Dominant, with Focally Folded Myelin Sheaths, Type 1B; Charcot-Marie-Tooth Disease, Slow Nerve Conduction Type, Linked to Duffy; Charcot-Marie-Tooth Neuropathy, Type 1B; Hereditary Motor and Sensory Neuropathy I; HMSN I; Hereditary Motor and Sensory Neuropathy IB; HMSN IB; HMSN1; HMSN1B; Peroneal Muscular Atrophy
View all models View ALL (2) mouse models for this human disease.
Genes and
mouse models 		Mutations in human and/or mouse homologs are associated with this disease

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Mpz* MPZ* View 2 models 1:1 Homology
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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Funding Information
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Send questions and comments to User Support. 		last database update
05/22/2013
MGI 5.13 		The Jackson Laboratory