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Disease Ontology Browser
Finnish type amyloidosis (DOID:0050637)
Alliance: disease page
Synonyms: AGel amyloidosis; AMYLOIDOSIS, MERETOJA TYPE; gelsolin amyloidosis; Lattice corneal dystrophy type II
Alt IDs: OMIM:105120, ORDO:85448
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.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
MGI 6.22
The Jackson Laboratory