Version: 8.0.0
Date: Tue Jan 28 2025
Finnish type amyloidosis
DOID:0050637
SummaryAssociated GenesAssociated AllelesAssociated Models
Disease

Finnish type amyloidosis

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.
Synonyms
  • AGel amyloidosis
  • AMYLOIDOSIS, MERETOJA TYPE
Cross References
Parent Terms
Child Terms
None
Sources of Associations

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      Associated Models

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