Preferred Name | Retinitis Pigmentosa | |
Synonyms |
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Definitions |
* hereditary, progressive degeneration of the neuroepithelium of the retina characterized by night blindness and progressive contraction of the visual field. (MSH) * group of inherited abnormalities in the retina; characterized by night blindness, retinal atrophy, weakening of the retinal vessels, pigment clumping, and contraction of the visual field. (CSP) |
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ID |
http://uri.neuinfo.org/nif/nifstd/birnlex_12820 |
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createdDate |
2007-11-18 |
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definition |
* hereditary, progressive degeneration of the neuroepithelium of the retina characterized by night blindness and progressive contraction of the visual field. (MSH) * group of inherited abnormalities in the retina; characterized by night blindness, retinal atrophy, weakening of the retinal vessels, pigment clumping, and contraction of the visual field. (CSP) |
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editorial note | ||
hasBirnlexCurator | ||
hasCurationStatus | ||
hasDefinitionSource | ||
hasExternalSource | ||
label |
Retinitis Pigmentosa |
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MeshUid |
D012174 |
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modifiedDate |
2007-11-18 |
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note |
* hereditary, progressive degeneration of the neuroepithelium of the retina characterized by night blindness and progressive contraction of the visual field. (MSH) * group of inherited abnormalities in the retina; characterized by night blindness, retinal atrophy, weakening of the retinal vessels, pigment clumping, and contraction of the visual field. (CSP) |
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preferred label |
Retinitis Pigmentosa |
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synonym |
Chorioretinal heredodystrophy Pigmentary retinopathy Rod cone Dystrophy Tapetoretinal degeneration |
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UmlsCui |
C0035334 |
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subClassOf |