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Chorioretinal atrophy, progressive bifocal MeSH Supplementary Concept Data 2025


MeSH Supplementary
Chorioretinal atrophy, progressive bifocal
Unique ID
C535356
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C535356
Entry Term(s)
CRAPB Chorioretinal atrophy progressive bifocal
PBCRA Progressive bifocal chorioretinal atrophy
Progressive bifocal chorioretinal atrophy
Registry Numbers
0
Heading Mapped to
*Corneal Dystrophies, Hereditary
Frequency
45
Note
A rare, autosomal dominant congenital chorioretinal dystrophy. The disorder is characterized by progressive macular and nasal retinal atrophic lesions, NYSTAGMUS; MYOPIA, and poor vision There are 2 distinct foci of atrophy, a temporal focus that is present at birth and a nasal focus that appears early in life. RETINAL DETACHMENT is an additional complication of the disease. OMIM: 600790
Date of Entry
2010/08/25
Revision Date
2019/06/19
Chorioretinal atrophy, progressive bifocal Preferred
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