MeSH Browser

MeSH Supplementary: Leber Congenital Amaurosis 4
Unique ID: C565778
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565778
Entry Term(s): Cone-Rod Dystrophy, Aipl1-Related; Retinitis Pigmentosa, Juvenile, Aipl1-Related
Registry Number: 0
Heading Mapped to: *Leber Congenital Amaurosis
Frequency: 3
Date of Entry: 2012/11/05

Leber Congenital Amaurosis 4 MeSH Supplementary Concept Data 2024