Term Name: autosomal dominant distal hereditary motor neuronopathy 15
Synonyms:
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.
Ontology: Human Disease [DOID:0051042]   ( DOID:0051042 )

Relationships
is a type of: autosomal dominant distal hereditary motor neuronopathy