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Summary Literature (0)
MIM:105200 - AMYLOIDOSIS, HEREDITARY SYSTEMIC 2; AMYLD2

Xenbase Genes: fga, lyz, b2m, apoa1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007099 - familial visceral amyloidosis

Disease Ontology (DO):
DOID:0050636 - familial visceral amyloidosis