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Amyotrophic lateral sclerosis 17
Disease Summary
Associated Targets (1)
Tbio
1
Uniprot Description An adult-onset progressive neurodegenerative disorder with predominantly lower motor neuron involvement, manifest as muscle weakness and wasting of the upper and lower limbs, bulbar signs, and respiratory insufficiency.
DataSource References
UniProt Disease: OMIM:614696
Monarch: OMIM:614696
Use Cases
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Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
UniProt Disease
Monarch
High level summary of knowledge for a disease, including descriptions and datasource references.