About: familial benign fleck retina

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

Attributes	Values
type	Class
subClassOf	autosomal recessive disease retinal disease nodeID://b50945258
label	familial benign fleck retina
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0111677
database_cross_reference	MESH:C565564 OMIM:228980 ORDO:363989 SNOMEDCT_US_2021_09_01:770434009 UMLS_CUI:C1856718
has_exact_synonym	FRFB (en)
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A retinal disease characterized by a striking pattern of diffuse, yellow-white, fleck-like lesions extending to the far periphery of the retina but with no apparent visual or electrophysiologic deficits that has_material_basis_in homozygous or compound heterozygous mutation in PLA2G5 on chromosome 1p36.13.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50945259

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