MeSH Browser

MeSH Heading: Cone-Rod Dystrophies
Tree Number(s): C11.270.152; C11.768.585.658.250; C16.320.290.152
Unique ID: D000071700
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D000071700
Annotation: ROD CONE DYSTROPHIES see RETINITIS PIGMENTOSA is also available
Scope Note: Genetically heterogeneous and sometimes syndromic (e.g., BARDET BIEDL SYNDROME; and SPINOCEREBELLAR ATAXIA TYPE 7) retinopathies with initial RETINAL CONE involvement. They are characterized by decreased VISUAL ACUITY; COLOR VISION DEFECTS; progressive loss of peripheral vision and night blindness.
Entry Term(s): Cone-Rod Degenerations; Cone-Rod Dystrophy; Cone-Rod Dystrophy 2; Cone-Rod Retinal Dystrophy; Retinal Cone-Rod Dystrophy; Rod Cone Dystrophies; Rod-Cone Dystrophy
Previous Indexing: Retinal Degeneration (1975-2016); Retinitis Pigmentosa (1981-2016)
Public MeSH Note: 2017; see RETINITIS PIGMENTOSA 2011-2016
History Note: 2017; use RETINITIS PIGMENTOSA 2011-2016
Date Established: 2017/01/01
Date of Entry: 2016/07/05
Revision Date: 2018/06/30

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)

Cone-Rod Dystrophies MeSH Descriptor Data 2025