Finnish type amyloidosis (DOID:0050637)
Alliance: disease page
Synonyms: AGel amyloidosis; AMYLOIDOSIS, MERETOJA TYPE; gelsolin amyloidosis; Lattice corneal dystrophy type II
Alt IDs: OMIM:105120, ORDO:85448
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.