Preferred Label : White Dot Syndromes;
MeSH definition : A group of idiopathic multifocal posterior uveitis syndromes involving the CHOROID;
RETINAL PIGMENT EPITHELIUM; and RETINA. They are characterized by multiple lesions
of hypoautofluorescent dots in the FUNDUS OCULI and reduced VISUAL ACUITY. Several
entities including BIRDSHOT CHORIORETINOPATHY are HLA-A ANTIGENS serotype A29 positive.;
Définition CISMeF : White dot syndromes are inflammatory diseases characterized by the presence of white
dots on the fundus, the interior surface of the eye. The majority of individuals affected
with white dot syndromes are younger than fifty years of age. Some symptoms include
blurred vision and visual field loss. There are many theories for the etiology of
white dot syndromes including infectious, viral, genetics and autoimmune. Classically
recognized white dot syndromes include: Acute posterior multifocal placoid pigment
epitheliopathy (APMPPE); Birdshot chorioretinopathy; Multiple evanescent white dot
syndrome (MEWDS); Acute zonal occult outer retinopathy (AZOOR) Multifocal choroiditis
and panuveitis (MCP) Punctate inner choroiditis (PIC); Serpiginous choroiditis
(source https://en.wikipedia.org/wiki/White_dot_syndromes).;
MeSH synonym : White Dot Syndrome;
MeSH Hyperonym : Acute Macular Neuroretinopathies; Macular Neuroretinopathy, Acute; Neuroretinopathy, Acute Macular;
MeSH hyponym : Choroidopathy, Punctate Inner; Inner Choroidopathy, Punctate; Punctate Inner Choroidopathies; MEWDS; APMPPE; Choroiditis, Serpiginous; Serpiginous Choroiditides; Serpiginous Choroidopathy; Choroidopathy, Serpiginous; Serpiginous Choroidopathies;
Wikipedia link : https://en.wikipedia.org/wiki/White dot syndromes;
Origin ID : D000080363;
UMLS CUI : C1532959;
Allowable qualifiers
Automatic exact mappings (from CISMeF team)
Currated CISMeF NLP mapping
Record concept(s)
Related MeSH Supplementary Concept(s)
Semantic type(s)
UMLS correspondences (same concept)
A group of idiopathic multifocal posterior uveitis syndromes involving the CHOROID;
RETINAL PIGMENT EPITHELIUM; and RETINA. They are characterized by multiple lesions
of hypoautofluorescent dots in the FUNDUS OCULI and reduced VISUAL ACUITY. Several
entities including BIRDSHOT CHORIORETINOPATHY are HLA-A ANTIGENS serotype A29 positive.
White dot syndromes are inflammatory diseases characterized by the presence of white
dots on the fundus, the interior surface of the eye. The majority of individuals affected
with white dot syndromes are younger than fifty years of age. Some symptoms include
blurred vision and visual field loss. There are many theories for the etiology of
white dot syndromes including infectious, viral, genetics and autoimmune. Classically
recognized white dot syndromes include: Acute posterior multifocal placoid pigment
epitheliopathy (APMPPE); Birdshot chorioretinopathy; Multiple evanescent white dot
syndrome (MEWDS); Acute zonal occult outer retinopathy (AZOOR) Multifocal choroiditis
and panuveitis (MCP) Punctate inner choroiditis (PIC); Serpiginous choroiditis
(source https://en.wikipedia.org/wiki/White_dot_syndromes).