amyloidosis, hereditary, transthyretin-related Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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://www.omim.org/entry/105210
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Genes

1 genes associated with the amyloidosis, hereditary, transthyretin-related phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
TTR transthyretin