A rare hereditary amyloidosis that incorporates deposition of amyloid microfibril material in the lung parenchyma.
Comprehensive, easy-to-understand information about this condition
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cerebral amyloid angiopathy
MONDO:0005620
Finnish type amyloidosis
MONDO:0007097
familial visceral amyloidosis
MONDO:0007099
familial amyloid neuropathy
MONDO:0007100
familial primary localized cutaneous amyloidosis
MONDO:0007101
variant ABeta2M amyloidosis
MONDO:0017810