FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term Finnish type amyloidosis ID (Ontology) DOID:0050637 (Human Disease)
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.
Also Known As "AGel amyloidosis" ; "AMYLOIDOSIS, MERETOJA TYPE" ; "gelsolin amyloidosis" (for all, see Synonyms field below)
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
    Results list data from multiple species. Click on a button above and use the 'Filter by species' options on the resulting HitList to retrieve species-specific data.
Records annotated with this exact term (annotations to child terms are NOT included)
No relevant records available
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Genes
 Finnish type amyloidosis       2
 for disease ribbon | Finnish type amyloidosis       2
 model of | Finnish type amyloidosis       2
Spanning Tree (Parents/Children)
Only view relationship: 
sensory system disease
 |__eye disease____________________
autosomal genetic disease          |
 |__autosomal dominant disease_____|
skin disease                       |
 |__primary cutaneous amyloidosis__|
inherited metabolic disorder       |
 |__primary cutaneous amyloidosis__|
amyloidosis                        |
 |__primary cutaneous amyloidosis__|
                                   Finnish type amyloidosis  2 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a primary cutaneous amyloidosis
autosomal dominant disease
eye disease
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "AGel amyloidosis" EXACT
    "AMYLOIDOSIS, MERETOJA TYPE" EXACT
    "gelsolin amyloidosis" EXACT
    "Lattice corneal dystrophy type II" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
GARD:2339
MIM:105120
ORDO:85448