Familial encephalopathy with neuroserpin inclusion bodies Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C536841
Similar Terms
Downloads & Tools

Genes

1 genes/proteins associated with the disease Familial encephalopathy with neuroserpin inclusion bodies from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SERPINI1 serpin peptidase inhibitor, clade I (neuroserpin), member 1 2.88009