| Human Disease |
Hypertrophic Neuropathy of Dejerine-Sottas OMIM ID: 145900 |
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| Synonyms | Charcot-Marie-Tooth Disease, Type 3; CMT3; Dejerine-Sottas Neuropathy; DSN; Dejerine-Sottas Syndrome; DSS; Hereditary Motor and Sensory Neuropathy Type III; HMSN3 | ||||||||||||||||||||||||||||||||||||
| View all models | View ALL (1) mouse models for this human disease. | ||||||||||||||||||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Mpztm1Msch/Mpztm1Msch |
involves: 129S7/SvEvBrd | J:42838 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/05/2013 MGI 5.13 |
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