MeSH Browser

MeSH Heading: Retinitis Pigmentosa
Tree Number(s): C11.270.684; C11.768.585.658.500; C16.320.290.684
Unique ID: D012174
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D012174
Annotation: note entry term ROD CONE DYSTROPHIES: CONE-ROD DYSTROPHIES is also available
Scope Note: Hereditary, progressive degeneration of the retina due to death of ROD PHOTORECEPTORS initially and subsequent death of CONE PHOTORECEPTORS. It is characterized by deposition of pigment in the retina.
Entry Term(s): Pigmentary Retinopathy; Tapetoretinal Degeneration
NLM Classification #: WW 273
See Also: Tangier Disease
Date Established: 1966/01/01
Date of Entry: 1999/01/01
Revision Date: 2018/06/29

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)

Retinitis Pigmentosa MeSH Descriptor Data 2024