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Human Disease and Mouse Model Detail
Human Disease Neuronopathy, Distal Hereditary Motor, Type I; HMN1
OMIM ID: 182960
Synonyms Charcot-Marie-Tooth Disease, Spinal, I; Hmn I; Neuronopathy, Distal Hereditary Motor; Neuropathy, Distal Hereditary Motor, Type I; DHMN1; Spinal Muscular Atrophy, Distal, Juvenile, Autosomal Dominant, I
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
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last database update
MGI 6.03
The Jackson Laboratory