autosomal dominant distal hereditary motor neuronopathy 15 Disease Ontology Browser

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Disease Ontology Browser

autosomal dominant distal hereditary motor neuronopathy 15 (DOID:0051042)
Alliance: disease page
Alt IDs: OMIM:621094
Definition: An autosomal dominant distal hereditary motor neuronopathy that is characterized by adult onset of slowly progressive distal weakness and atrophy of the lower limbs associated with absent reflexes and that has_material_basis_in heterozygous mutation in the BAG3 gene on chromosome 10q26.

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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