X-linked retinal dysplasia

Orpha code: 1852OMIM code: 312550

Definicja

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
Klasyfikacja

Disease

Kod ORPHA
1852
Kod OMIM
312550
Kod ICD10
Q14.1
Kod ICD11
-

No additional description.

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