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Amyloidosis, Hereditary, Transthyretin-Related MeSH Supplementary Concept Data 2024

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MeSH Supplementary: Amyloidosis, Hereditary, Transthyretin-Related
Unique ID: C567782
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567782
Entry Term(s): Familial Transthyretin Cardiac Amyloidosis; Hereditary Amyloidosis, Transthyretin-Related; Transthyretin Amyloidosis; hereditary transthyretin amyloidosis
Registry Number: 0
Heading Mapped to: *Amyloid Neuropathies, Familial
Frequency: 1099
Note: Hereditary disorder characterized by AMYLOID DEPOSITS in the EXTRACELLULAR MATRIX of different tissues. Patients present POLYNEUROPATHY; CARPAL TUNNEL SYNDROME, autonomic insufficiency, CARDIOMYOPATHY, and gastrointestinal symptoms. A dominant mutation (V30M) in the TTR gene has been identified. OMIM: 105210
Date of Entry: 2012/11/05
Revision Date: 2019/01/16

Amyloidosis, Hereditary, Transthyretin-Related Preferred

Concept UI: M0568082
Registry Number: 0
Terms: Amyloidosis, Hereditary, Transthyretin-Related Preferred Term
Term UI T811060
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Hereditary Amyloidosis, Transthyretin-Related
Term UI T811063
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Transthyretin Amyloidosis
Term UI T811061
Date11/15/2011
LexicalTag NON
ThesaurusID; hereditary transthyretin amyloidosis
Term UI T000950521
Date01/16/2019
LexicalTag NON
ThesaurusID NLM (2019); Familial Transthyretin Cardiac Amyloidosis
Term UI T000867056
Date09/23/2014
LexicalTag NON
ThesaurusID NLM (2014)

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