Term Name:	Finnish type amyloidosis
Synonyms:	AGel amyloidosis, AMYLOIDOSIS, MERETOJA TYPE, gelsolin amyloidosis, Lattice corneal dystrophy type II
Definition:	An amyloidosis that is characterized by abnormal deposits of amyloid protein that mainly affect the eyes, nerves and skin and has_material_basis_in mutations in the gelsolin gene (GSN), and has_symptom corneal lattice dystrophy, has_symptom bilateral facial paralysis, has_symptom cutis laxa.
Ontology:	Human Disease [DOID:0050637]   ( DOID:0050637 )