MeSH Browser

MeSH Supplementary: RHYNS syndrome
Unique ID: C537612
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537612
Entry Term(s): Retinitis pigmentosa syndrome; Retinitis pigmentosa, HYpopituitarism, Nephronophthisis, and mild Skeletal dysplasia
Registry Number: 0
Heading Mapped to: *Hypopituitarism; *Retinitis Pigmentosa
Frequency: 3
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

RHYNS syndrome MeSH Supplementary Concept Data 2024