MeSH Browser

MeSH Supplementary: Rod-Cone Dystrophy, Sensorineural Deafness, and Fanconi-Type Renal Dysfunction
Unique ID: C564829
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564829
Registry Numbers: 0
Heading Mapped to: *Fanconi Syndrome; *Hearing Loss, Sensorineural; *Retinitis Pigmentosa
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Rod-Cone Dystrophy, Sensorineural Deafness, and Fanconi-Type Renal Dysfunction MeSH Supplementary Concept Data 2025