About   Help   FAQ
Disease Ontology Browser
transthyretin amyloidosis (DOID:0050638)
Alliance: disease page
Synonyms: Amyloidosis, hereditary, transthyretin-related; Corino de Andrade's disease; familial amyloid polyneuropathy; Familial transthyretin amyloidosis; transthyretin-related hereditary amyloidosis; TTR amyloidosis
Alt IDs: OMIM:105210
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.

Disease References using Mouse Models (4)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
12/05/2017
MGI 6.11
The Jackson Laboratory