|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A neurodegenerative disease that is characterized by intraneuronal inclusions of mutant neuroserpin resulting in progressive encephalopathy, dementia and seizures and has_material_basis_in a mutation in the SERPINI1 gene inherited in an in autosomal dominant pattern. (Human Disease Ontology, DOID_0050831)|
|Downloads & Tools|
1 genes/proteins associated with the disease Familial encephalopathy with neuroserpin inclusion bodies from the curated CTD Gene-Disease Associations dataset.
|SERPINI1||serpin peptidase inhibitor, clade I (neuroserpin), member 1||2.88009|