amyloidosis, hereditary, Transthyretin-Related

Preferred Label : amyloidosis, hereditary, Transthyretin-Related;

MeSH synonym : hereditary amyloidosis, Transthyretin-Related; transthyretin amyloidosis; Familial Transthyretin Cardiac Amyloidosis; hereditary transthyretin amyloidosis;

Details

Origin ID

C567782;

UMLS CUI

C2751492;

Currated CISMeF NLP mapping
- Amyloidosis, hereditary systemic 1 [OMIM Phenotype]
- hereditary transthyretin related amyloidosis [Disease (Nov.)]
MeSH term(s) associated for indexing
- amyloid neuropathies, familial [MeSH Descriptor]
Record concept(s)
- amyloidosis, hereditary, Transthyretin-Related [MeSH concept]
See also inter- (CISMeF)
- Cardiac Amyloidosis [NCIt concept]
- Senile cardiac amyloidosis (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Amyloidosis, hereditary systemic 1 [OMIM Phenotype]
- hereditary transthyretin related amyloidosis [Disease (Nov.)]
Validated automatic mappings to BTNT
- Hereditary Cardiac ATTR Amyloidosis [NCIt concept]
Validated automatic mappings to NTBT
- Transthyretin-mediated amyloidosis [MedDRA LLT]
- transthyretin amyloidosis [DO Concept]

Keyword's position in hierarchy(ies) :

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