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DO Term : scleromalacia perforans [DOID:14230] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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:
  • UMLS_CUI:C0155354,
  • SNOMEDCT_US_2023_03_01:26664005,
  • ICD10CM:H15.05,
  • ICD9CM:379.04
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