Human Disease and Mouse Model Detail
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Human Disease
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Neuronopathy, Distal Hereditary Motor, Type IIA; HMN2A
OMIM ID: 158590
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Synonyms
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Charcot-Marie-Tooth Disease, Spinal, I;
Charcot-Marie-Tooth Disease, Spinal, IIA;
Dhmn1;
Dhmn2a;
Hmn I;
Hmn IIA;
Neuropathy, Distal Hereditary Motor, Type I;
Neuropathy, Distal Hereditary Motor, Type IIA;
Spinal Muscular Atrophy, Distal, Adult, Autosomal Dominant, IIA;
Spinal Muscular Atrophy, Distal, Juvenile, Autosomal Dominant, I
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Gene is associated with the disease in this species |
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Hspb8
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HSPB8*
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1:1 Homology
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Analysis Tools