|Dataset||GAD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An amyloidosis that is characterized by a loss of sensation in the extremities, cardiomyopathy, nephropathy, vitreous opacities, and CNS amyloidosis resulting from abnormal deposits of amyloid protein in the body's organs and tissues and has_material_basis_in autosomal dominant inheritance of mutations in the TTR gene. (Human Disease Ontology, DOID_0050638)|
|Downloads & Tools|
2 genes associated with the disease familial amyloid polyneuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.