familial restrictive cardiomyopathy ATTRV122I amyloidosis https://github.com/monarch-initiative/mondo/issues/7330 https://www.malacards.org/card/attrv122i_amyloidosis SCTID:715655000 UMLS:C4275067 icd11.foundation:1449168185 MONDO:0019441 MEDGEN:907865 Orphanet:85451 ATTRV122I-related amyloidosis GARD:0016755 A rare hereditary Transthyretin (TTR)-related systemic amyloidosis (ATTR) with predominant cardiac involvement resulting from myocardial infiltration of abnormal amyloid protein. amyloidosis, hereditary systemic 1 obsolete_ATTRV122I amyloidosis