Disease-gene associations mined from literature

Human genes for Coats disease

Coats disease [DOID:7765]

Coats’ disease, (also known as exudative retinitis or retinal telangiectasis, sometimes spelled Coates' disease), is a very rare congenital, nonhereditary eye disorder, causing full or partial blindness, characterized by abnormal development of blood vessels behind the retina.

Synonyms:  Coats disease,  Coats disorder,  Coats syndrome,  DOID:7765,  Coats' disease (disorder) ...

Linkouts:  OMIM