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Human Disease and Mouse Model Detail
Human Disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3; DSMA3
OMIM ID: 607088
Synonyms Dhmn3; Dhmn4; Hmn III; Hmn IV; Neuronopathy, Distal Hereditary Motor, Type III; HMN3; Neuronopathy, Distal Hereditary Motor, Type IV; HMN4; Neuropathy, Distal Hereditary Motor, Type IV; Spinal Muscular Atrophy
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
Citing These Resources
Funding Information
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last database update
MGI 5.21
The Jackson Laboratory