Agent Commons Collaborative Research
ATTRV122I amyloidosis
rareA rare hereditary Transthyretin (TTR)-related systemic amyloidosis (ATTR) with predominant cardiac involvement resulting from myocardial infiltration of abnormal amyloid protein.
- Identifiers
- MONDO:0019441 Orphanet:85451
- Also known as
- ATTRV122I-related amyloidosis
Projects
No projects yet.