| Descriptor English: | Cone-Rod Dystrophies | ||||||
| Descriptor Spanish: |
Distrofias de Conos y Bastones
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| Descriptor Portuguese: | Distrofias de Cones e Bastonetes | ||||||
| Descriptor French: | Dystrophies des cônes et des batonnets | ||||||
| Entry term(s): |
Cone Rod Degenerations Cone Rod Dystrophies Cone Rod Dystrophy Cone Rod Dystrophy 2 Cone Rod Retinal Dystrophy Cone-Rod Degeneration Cone-Rod Degenerations Cone-Rod Dystrophies, Retinal Cone-Rod Dystrophy Cone-Rod Dystrophy 2 Cone-Rod Dystrophy, Retinal Cone-Rod Retinal Dystrophies Cone-Rod Retinal Dystrophy Retinal Cone Rod Dystrophy Retinal Cone-Rod Dystrophies Retinal Cone-Rod Dystrophy Retinal Dystrophies, Cone-Rod Retinal Dystrophy, Cone-Rod Rod Cone Dystrophies Rod Cone Dystrophy Rod-Cone Dystrophies Rod-Cone Dystrophy |
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| Tree number(s): |
C11.270.152 C11.768.585.658.250 C16.320.290.152 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D000071700 | ||||||
| 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. |
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| Annotation: | ROD CONE DYSTROPHIES see RETINITIS PIGMENTOSA is also available |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Previous Indexing: |
Retinal Degeneration (1975-2016) Retinitis Pigmentosa (1981-2016) |
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| Public MeSH Note: | 2017; see RETINITIS PIGMENTOSA 2011-2016 |
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| History Note: | 2017; use RETINITIS PIGMENTOSA 2011-2016 |
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| DeCS ID: | 56390 | ||||||
| Unique ID: | D000071700 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2017/01/01 | ||||||
| Date of Entry: | 2016/07/05 | ||||||
| Revision Date: | 2018/06/30 |
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DISEASES
Eye Diseases [C11]Eye Diseases -
DISEASES
Eye Diseases [C11]Eye Diseases
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Cone-Rod Dystrophies
- Preferred
Cone-Rod Dystrophy 2
- Narrower
Rod-Cone Dystrophy
- Narrower
| Concept UI |
M000615345 |
| 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. |
| Preferred term | Cone-Rod Dystrophies |
| Entry term(s) |
Cone Rod Degenerations Cone Rod Dystrophies Cone Rod Dystrophy Cone Rod Retinal Dystrophy Cone-Rod Degeneration Cone-Rod Degenerations Cone-Rod Dystrophies, Retinal Cone-Rod Dystrophy Cone-Rod Dystrophy, Retinal Cone-Rod Retinal Dystrophies Cone-Rod Retinal Dystrophy Retinal Cone Rod Dystrophy Retinal Cone-Rod Dystrophies Retinal Cone-Rod Dystrophy Retinal Dystrophies, Cone-Rod Retinal Dystrophy, Cone-Rod |
| Concept UI |
M0574754 |
| Preferred term | Cone-Rod Dystrophy 2 |
| Entry term(s) |
Cone Rod Dystrophy 2 |
| Concept UI |
M000643634 |
| Preferred term | Rod-Cone Dystrophy |
| Entry term(s) |
Rod Cone Dystrophies Rod Cone Dystrophy Rod-Cone Dystrophies |
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