Cone-Rod Dystrophies [inverzní retinopathia pigmentosa]
- Terms
-
degenerace čípků a tyčinek
dystrofie čípků a tyčinek
dystrofie čípků a tyčinek 2
dystrofie čípků a tyčinek sítnice
inverzní retinitis pigmentosa
inverzní retinopathia pigmentosa 2
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Cone-Rod Degenerations
Cone-Rod Dystrophy
Cone-Rod Dystrophy 2
Cone-Rod Retinal Dystrophy
Retinal Cone-Rod Dystrophy
Rod Cone Dystrophies
Rod-Cone Dystrophy
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.
- Annotation
- ROD CONE DYSTROPHIES see RETINITIS PIGMENTOSA is also available
- DUI
- D000071700 MeSH Browser
- CUI
- M000615345
- Previous indexing
- Retinal Degeneration (1975-2016); Retinitis Pigmentosa (1981-2016)
- History note
- 2017; use RETINITIS PIGMENTOSA 2011-2016
- Public note
- 2017; see RETINITIS PIGMENTOSA 2011-2016
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification
- CO
- complications
- DI
- diagnosis
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology
- EH
- ethnology
- ET
- etiology
- GE
- genetics
- HI
- history
- IM
- immunology
- ME
- metabolism
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology
- PP
- physiopathology
- PC
- prevention & control
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery
- TH
- therapy
- UR
- urine
- VE
- veterinary
- VI
- virology
Jalili syndrome Disease MeSH Browser