MeSH Browser

MeSH Supplementary: Stickler Syndrome, Type I, Nonsyndromic Ocular
Unique ID: C563709
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563709
Entry Term(s): Stickler Syndrome, Atypical; Stickler Syndrome, Type I, Predominantly Ocular
Registry Number: 0
Heading Mapped to: *Eye Diseases, Hereditary
Frequency: 1
Note: mutation in COL2A1
Date of Entry: 2012/11/05

Stickler Syndrome, Type I, Nonsyndromic Ocular MeSH Supplementary Concept Data 2024