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. [ url:https://rarediseases.info.nih.gov/diseases/2339/familial-amyloidosis-finnish-type http://purl.obolibrary.org/obo/ECO_0007637 ]
Synonyms: gelsolin amyloidosis Lattice corneal dystrophy type II AGel amyloidosis AMYLOIDOSIS, MERETOJA TYPE
Term information
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- autosomal dominant disease
- eye disease
- primary cutaneous amyloidosis
- disease has location some eye
- disease has location some zone of skin
- has symptom some facial paralysis
- disease has feature some lattice corneal dystrophy
- has material basis in some autosomal dominant inheritance
- disease has location some nerve
- disease has feature some cutis laxa