D015792Level 4
Retinal Dysplasia
**Definition:** Congenital, often bilateral, retinal abnormality characterized by the arrangement of outer nuclear retinal cells in a palisading or radiating pattern surrounding a central ocular space. This disorder is sometimes hereditary.
**Tree numbers:** - C11.250.666 - C11.270.660 - C11.768.660 - C16.131.384.784 - C16.320.290.660
GET
/api/v1/systems/mesh/nodes/D015792Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.