Finnish type amyloidosis

MONDO:0007097

Also known as: amyloidosis, MERETOJA type, familial amyloid polyneuropathy type IV, familial amyloidosis, Finnish type, gelsolin amyloidosis, hereditary amyloidosis, Finnish type, meretoja syndrome, AGel amyloidosis, amyloid cranial neuropathy with lattice corneal dystrophy

16 clinical trials for this condition and its sub-types, 0 tagged with Finnish type amyloidosis itself.

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Where it sits in the disease tree

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Part of

↑ Syndromic disease (7133) ↑ Hereditary peripheral neuropathy (478) ↑ Hereditary amyloidosis (79) ↑ Corneal dystrophy (60)

Including sub-types (16) Tagged with Finnish type amyloidosis (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.