About: Finnish type amyloidosis

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An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

OMIM mapping confirmed by DO. [SN].

Attributes	Values
type	Class
subClassOf	primary cutaneous amyloidosis autosomal dominant disease eye disease nodeID://b50937299 nodeID://b50937300 nodeID://b50937301 nodeID://b50937302
label	Finnish type amyloidosis
comment	OMIM mapping confirmed by DO. [SN].
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0050637
database_cross_reference	GARD:2339 OMIM:105120 ORDO:85448
has_exact_synonym	AGel amyloidosis AMYLOIDOSIS, MERETOJA TYPE (en) Lattice corneal dystrophy type II gelsolin amyloidosis
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	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_symptoms corneal lattice dystrophy, has_symptom bilateral facial paralysis, has_symptom cutis laxa.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50937303

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