autosomal dominant distal hereditary motor neuronopathy 10 Disease Ontology Browser

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autosomal dominant distal hereditary motor neuronopathy 10 (DOID:0081399)
Alliance: disease page
Alt IDs: OMIM:620080
Definition: An autosomal dominant distal hereditary motor neuronopathy that is characterized clinically by length-dependent motor neuropathy primarily affecting the lower limbs and that has_material_basis_in heterozygous mutation in the EMILIN1 gene on chromosome 2p23.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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