|OBO ID: DOID:0050638|
|Term Name:||transthyretin amyloidosis||Search Ontology:|
|Definition:||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. (7)|
|Ontology:||Human Disease (DOID:0050638)|
|is a type of:||
OTHER transthyretin amyloidosis PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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