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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 (7)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
MGI 6.14
The Jackson Laboratory