MeSH Browser

MeSH Heading: White Dot Syndromes
Tree Number(s): C11.941.879.780.900.650
Unique ID: D000080363
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D000080363
Scope Note: 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.
Entry Term(s): APMPPE; Acute Idiopathic Blind Spot Enlargement Syndrome; Acute Macular Neuroretinopathy; Acute Posterior Multifocal Placoid Pigment Epitheliopathy; Diffuse Subretinal Fibrosis Uveitis; MEWDS; Multiple Evanescent White Dot Syndrome; Punctate Inner Choroidopathy; Serpiginous Choroiditis; Serpiginous Choroidopathy
Previous Indexing: Retinal Diseases (1992-2019)
Public MeSH Note: 2020
History Note: 2020
Date Established: 2020/01/01
Date of Entry: 2019/07/08
Revision Date: 2020/02/06

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

congenital (CN)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

White Dot Syndromes MeSH Descriptor Data 2024