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Human Disease

scleromalacia perforans

Term ID
DOID:14230
Synonyms
Definition
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. (2)
References
  • ICD10CM:H15.05
  • ICD9CM:379.04
  • SNOMEDCT_US_2023_03_01:26664005
  • UMLS_CUI:C0155354
Ontology
Human Disease   ( DOID:14230 )
Relationships
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Genes Involved
Zebrafish Models