MeSH Browser

MeSH Supplementary: Oculodental syndrome Rutherfurd syndrome
Unique ID: C537732
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537732
Entry Term(s): Corneal dystrophy with gum hypertrophy; Gingival Hypertrophy With Corneal Dystrophy; Gingival hypertrophy corneal dystrophy; Rutherfurd syndrome
Registry Number: 0
Heading Mapped to: *Corneal Dystrophies, Hereditary; *Gingival Hypertrophy
Frequency: 1
Date of Entry: 2010/08/25
Revision Date: 2012/08/24

Oculodental syndrome Rutherfurd syndrome MeSH Supplementary Concept Data 2023