MeSH Browser

MeSH Supplementary: Spondyloepiphyseal Dysplasia With Punctate Corneal Dystrophy
Unique ID: C566660
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566660
Registry Numbers: 0
Heading Mapped to: *Corneal Dystrophies, Hereditary; *Osteochondrodysplasias
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 2012/11/05

Spondyloepiphyseal Dysplasia With Punctate Corneal Dystrophy MeSH Supplementary Concept Data 2025