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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)

Trials to join now! 10 Not yet recruiting 1 Completed 4 Terminated 1

Could a simple blood test track nerve damage? a study investigates NT-3 levels in neuropathy.

Knowledge-focused Stopped early

This study measures levels of a protein called NT-3 in the blood of people with peripheral neuropathy or Charcot-Marie-Tooth disease. Researchers will compare these levels with measures of muscle strength, mobility, and daily function. The goal is to see whether NT-3 levels corre…

Sponsor: Zarife Sahenk • Aim: Knowledge-focused

Last updated Jul 31, 2026 00:00 UTC