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Autosomal dominant rhegmatogenous retinal detachment

Disease Export to PDF
Name:
Autosomal dominant rhegmatogenous retinal detachment
Description:
A rare, hereditary, non-syndromic form of vitreoretinopathy characterized by retinal tears due to abnormal vitreous, and commonly present refractive errors. No other signs or symptoms of Stickler syndrome is present.
ORPHAcode:
209867
XREF(s):
Orphanet
ICD-10
OMIM
Analyte(s):
COL2A1
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14