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Retinal Dysplasia MeSH Descriptor Data 2022


MeSH Heading
Retinal Dysplasia
Tree Number(s)
C11.250.666
C11.270.660
C11.768.660
C16.131.384.784
C16.320.290.660
Unique ID
D015792
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D015792
Annotation
do not use /‌congen & do not coord with INFANT, NEWBORN, DISEASES
Scope Note
Congenital, often bilateral, retinal abnormality characterized by the arrangement of outer nuclear retinal cells in a palisading or radiating pattern surrounding a central ocular space. This disorder is sometimes hereditary.
Previous Indexing
Retina/abnormalities (1966-1989)
Retinal Degeneration (1970-1989)
Public MeSH Note
90
History Note
90
Date Established
1990/01/01
Date of Entry
1989/05/25
Revision Date
2001/07/25
Retinal Dysplasia Preferred
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