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 )
Relationships
is a type of:
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
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.