Human genes for Finnish type amyloidosis
Finnish type amyloidosis [DOID:0050637]
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.
Synonyms: Finnish type amyloidosis, DOID:0050637, Finnish type amyloidosises, AGel amyloidosis, AMYLOIDOSIS, MERETOJA TYPE ...
Linkouts: OMIM