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Metadata
ID DOID:14230
Name scleromalacia perforans
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.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5987604/, https://eyewiki.aao.org/Scleritis
Xrefs

ICD10CM:H15.05

ICD9CM:379.04

SNOMEDCT_US_2023_03_01:26664005

UMLS_CUI:C0155354

Parent Relationships

is_a scleral disease

Subclass Logical Relationships

has symptom some necrosis

has symptom some loss of vision

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