OBO ID: DOID:0050638
Term Name: transthyretin amyloidosis Search Ontology:
Synonyms:
  • Amyloidosis, hereditary, transthyretin-related
  • ATTR amyloidosis
  • ATTRm amyloidosis
  • Corino de Andrade's disease
  • familial amyloid polyneuropathy
  • Familial transthyretin amyloidosis
  • paramyloidosis
  • transthyretin-related hereditary amyloidosis
  • TTR amyloidosis
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)
References:
Ontology: Human Disease   (DOID:0050638)
OTHER transthyretin amyloidosis PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TTR Amyloidosis, hereditary, transthyretin-related 105210
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None