MeSH Browser

MeSH Heading: Stargardt Disease
Tree Number(s): C11.270.872; C11.768.585.439.339; C16.320.290.724
Unique ID: D000080362
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D000080362
Scope Note: A juvenile-onset macular dystrophy characterized by progressive loss of VISUAL ACUITY with normal acuity in peripheral VISUAL FIELDS. Other associated clinical features may include LIPOFUSCIN fundus autofluorescence, atrophy of the RETINAL PIGMENT EPITHELIUM, loss of color vision, PHOTOPHOBIA and PARACENTRAL SCOTOMA. Germline mutations in the ABCA4 gene have been identified in recessive and dominant diseases.
Entry Term(s): Fundus Flavimaculatus; Juvenile Macular Degeneration; Macular Degeneration, Juvenile; Macular Dystrophy With Flecks, Type 1; Stargardt Disease 1; Stargardt Macular Degeneration
Public MeSH Note: 2020; STARGARDT DISEASE was indexed under MACULAR DEGENERATION 2010-2019
History Note: 2020(2010)
Date Established: 2020/01/01
Date of Entry: 2019/07/08
Revision Date: 2019/04/29

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

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)

Concept UI: M000612272
Scope Note: A juvenile-onset macular dystrophy characterized by progressive loss of VISUAL ACUITY with normal acuity in peripheral VISUAL FIELDS. Other associated clinical features may include LIPOFUSCIN fundus autofluorescence, atrophy of the RETINAL PIGMENT EPITHELIUM, loss of color vision, PHOTOPHOBIA and PARACENTRAL SCOTOMA. Germline mutations in the ABCA4 gene have been identified in recessive and dominant diseases.
Terms: Stargardt Disease Preferred Term
Term UI T842534
Date04/18/2013
LexicalTag EPO
ThesaurusID GHR (2014); Fundus Flavimaculatus
Term UI T801321
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Stargardt Macular Degeneration
Term UI T842533
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014)

Stargardt Disease MeSH Descriptor Data 2023