Familial amyloid cardiomyopathy
GPTKB entity
Statements (32)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:disease
amyloidosis cardiomyopathy |
| gptkbp:affectsOrgan |
heart
|
| gptkbp:alternativeName |
ATTR-CM
hereditary transthyretin amyloid cardiomyopathy |
| gptkbp:causedBy |
hereditary amyloidosis
transthyretin gene mutation |
| gptkbp:hasDiagnosticMethod |
genetic testing
biopsy echocardiogram cardiac MRI |
| gptkbp:hasProteinDeposit |
transthyretin amyloid
|
| https://www.w3.org/2000/01/rdf-schema#label |
Familial amyloid cardiomyopathy
|
| gptkbp:ICD-10_code |
E85.1
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:MeSH_ID |
D000686
|
| gptkbp:OMIM |
105210
|
| gptkbp:onset |
adulthood
|
| gptkbp:prevalence |
rare
|
| gptkbp:riskFactor |
family history
African ancestry |
| gptkbp:symptom |
gptkb:arrhythmia
heart failure fatigue shortness of breath |
| gptkbp:treatment |
gptkb:tafamidis
supportive care liver transplant heart transplant |
| gptkbp:bfsParent |
gptkb:P02766
|
| gptkbp:bfsLayer |
8
|