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Sveinsson Chorioretinal Atrophy MeSH Supplementary Concept Data 2024


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
Registry Number
0
Heading Mapped to
*Corneal Dystrophies, Hereditary
*Retinal Degeneration
Frequency
8
Note
mutation in TEAD1
Date of Entry
2012/11/05
Sveinsson Chorioretinal Atrophy Preferred
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