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Retinal Aplasia MeSH Supplementary Concept Data 2025


MeSH Supplementary
Retinal Aplasia
Unique ID
C566720
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C566720
Entry Term(s)
Amaurosis Congenita
Registry Numbers
0
Heading Mapped to
*Blindness
*Retinal Diseases
*Eye Diseases, Hereditary
Frequency
2
Date of Entry
2012/11/05
Revision Date
2012/11/05
Retinal Aplasia Preferred
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