OBO ID: DOID:0111198 |
Term Name: | autosomal dominant distal hereditary motor neuronopathy | Search Ontology: | |
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Definition: | A spinal muscular atrophy that is characterized by progressive distal motor weakness and muscular atrophy of the peripheral nervous system without sensory impairment, that is caused by anterior horn cell degeneration, and that has_material_basis_in autosomal dominant inheritance. https://www.ncbi.nlm.nih.gov/pubmed/15358725 | ||
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Ontology: | Human Disease ( DOID:0111198 ) |
OTHER autosomal dominant distal hereditary motor neuronopathy PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS (1)
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