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Summary Literature (0)
MIM:105210 - AMYLOIDOSIS, HEREDITARY SYSTEMIC 1; AMYLD1

Xenbase Genes: ttr

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007100 - primary circulatory organ
MONDO:0019441 - ATTRV122I amyloidosis

Disease Ontology (DO):
DOID:0050638 - hereditary systemic amyloidosis 1