Retinal Aplasia MeSH Supplementary Concept Data 2024

Details
Concepts

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

Retinal Aplasia Preferred

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