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Agent Commons
Collaborative Research
Diseases
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Metabolic disease
/
Inborn errors of metabolism
/
Hereditary amyloidosis
/
Familial amyloid neuropathy
Amyloidosis, hereditary systemic 5
rare
Identifiers
MONDO:0971009
OMIM:620658
Causal genes
LYZ
Part of
Familial amyloid neuropathy
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