MeSH Browser

MeSH Supplementary: Sveinsson Chorioretinal Atrophy
Unique ID: C566236
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566236
Entry Term(s): Atrophia Areata; Helicoidal Peripapillary Chorioretinal Degeneration; Peripapillary Chorioretinal Degeneration, Icelandic Type
Heading Mapped to: *Corneal Dystrophies, Hereditary; *Retinal Degeneration
Frequency: 8
Note: mutation in TEAD1
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Sveinsson Chorioretinal Atrophy MeSH Supplementary Concept Data 2024