Scleromalacia Perforans
Disease ID: disease_node_20818
Connections displayed (default: 10).
Loading graph...
| Dbxref | ICD10CM:H15.05, ICD9CM:379.04, SNOMEDCT_US_2023_03_01:26664005, UMLS_CUI:C0155354 |
|---|---|
| Subclassof | DOID_11343 |
| Data Source | DOID |
| Doid Label | scleromalacia perforans |
| Doid 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. |
| Has Symptom | SYMP_0000321, SYMP_0000132 |
| Disease Node Id | disease_node_20818 |
| Doid Id | DOID_14230 |
| Label | Scleromalacia Perforans |
- Outgoing r'ship
HAS_SYMPTOMto/from Necrosis(ID:disease_node_5435;disease_node_21082) (Disease) - Outgoing r'ship
HAS_SYMPTOMto/from Loss Of Vision(ID:disease_node_21716) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Scleral Diseases(ID:disease_node_8230) (Disease)