Transthyretin amyloidosis

GPTKB entity

Statements (47)
Predicate Object
gptkbp:instance_of gptkb:neurodegenerative_diseases
gptkbp:affects gptkb:Heart
gptkb:computer
kidneys
gastrointestinal tract
gptkbp:associated_with gptkb:familial_amyloid_cardiomyopathy
gptkb:familial_amyloid_polyneuropathy
aging
gptkbp:caused_by transthyretin protein misfolding
gptkbp:clinical_trial ongoing studies
phase 1 trials
phase 2 trials
phase 3 trials
gptkbp:diagnosis genetic testing
biopsy
gptkbp:first_described_by gptkb:1952
gptkbp:genetic_studies TTR gene mutation
gptkbp:historical_significance collaboration among researchers
advancements in treatment options
greater public awareness
increased research interest
improved diagnostic techniques
https://www.w3.org/2000/01/rdf-schema#label Transthyretin amyloidosis
gptkbp:prevalence rare disease
gptkbp:public_awareness patient education
community support
research funding
advocacy groups
fundraising efforts
gptkbp:research_focus treatment efficacy
diagnostic methods
amyloid fibril formation
gptkbp:risk_factor family history
certain ethnic groups
gptkbp:symptoms heart failure
peripheral neuropathy
carpal tunnel syndrome
gptkbp:treatment gptkb:diflunisal
gptkb:tafamidis
improved quality of life
reduced symptoms
liver transplantation
slowed disease progression
increased survival rates
gptkbp:bfsParent gptkb:NTLA-2001
gptkb:NTLA-2002
gptkbp:bfsLayer 5