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)
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1 genes associated with the disease familial amyloid polyneuropathy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.