| Human Disease |
Neuronopathy, Distal Hereditary Motor, Type Va; HMN5A OMIM ID: 600794 |
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| Synonyms | Dhmn Va; Hmn Va; Neuronopathy, Distal Hereditary Motor, Type V; HMN5; Neuropathy, Distal Hereditary Motor, Type Va; DHMN5A; Spinal Muscular Atrophy, Distal, Type V; DSMAV; Spinal Muscular Atrophy, Distal, Type Va; DSMAVA; Spinal Muscular Atrophy, Distal, with Upper Limb Predominance | |||||||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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