X-linked retinal dysplasia

Definition

A rare genetic eye disease characterized by abnormal proliferation of retinal tissue resulting in the formation of retinal folds, thereby causing gliosis and, clinically, variable degrees of visual impairment. No clinical findings other than those associated with the eyes have been demonstrated.

Disease data

Classification

Disease

ORPHA code

1852

OMIM code

312550

ICD10 code

Q14.1

ICD11 code

*Soruce