MeSH Browser

MeSH Supplementary: Skeletal Dysplasia, Rhizomelic, with Retinitis Pigmentosa
Unique ID: C563806
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563806
Registry Numbers: 0
Heading Mapped to: *Bone Diseases, Developmental; *Retinitis Pigmentosa
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Skeletal Dysplasia, Rhizomelic, with Retinitis Pigmentosa MeSH Supplementary Concept Data 2025