DISEASES

Disease-gene associations mined from literature

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