Amyloidosis, Hereditary, Transthyretin-Related Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C567782
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Genes

1 genes/proteins associated with the disease Amyloidosis, Hereditary, Transthyretin-Related from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
TTR transthyretin 2.88009