Autosomal dominant rhegmatogenous retinal detachment

Orpha code: 209867OMIM code: 609508

Definition

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.

Disease data
Classification

Disease

ORPHA code
209867
OMIM code
609508
ICD10 code
H33.0
ICD11 code
9B73.0

No additional description.

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