MeSH Browser

MeSH Supplementary: Leber Congenital Amaurosis 14
Unique ID: C567636
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567636
Entry Term(s): Retinal Dystrophy, Early-Onset Severe, Lrat-Related; Retinitis Pigmentosa, Juvenile, Lrat-Related
Registry Number: 0
Heading Mapped to: *Retinitis Pigmentosa; *Leber Congenital Amaurosis
Frequency: 0
Date of Entry: 2012/11/05

Leber Congenital Amaurosis 14 MeSH Supplementary Concept Data 2024