Disease-gene associations mined from literature

Human genes for scleromalacia perforans

Scleromalacia perforans [DOID:14230]

A scleral disease that is characterized by a painless severe necrotizing scleritis where the sclera is white, avascular, and thin. The choroid can become exposed leading to infarction and necrosis of related areas; the sclera can also thin such that the dark uvea protrudes through the front of the eye, forming a staphyloma which has_symptom loss of vision and appearance of a dark bulge. Scleromalacia perforans is usually caused by a rare complication of autoimmune disease like rheumatoid arthritis.

Synonyms:  scleromalacia perforans,  DOID:14230,  scleromalacia perforanses