Corneal perforation
Symptom Information:
Symptom ID: | HPO:0100583 | ||||||||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): | |||||||||||||||||||||||||||||||||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the eye(HPO:0000478) Abnormal eye morphology(HPO:0012372) Abnormality of the globe(HPO:0012374) Abnormality of the anterior segment of the globe(HPO:0004328) Abnormality of the cornea(HPO:0000481) Corneal perforation(HPO:0100583) MedDRA: Eye disorders(MedDRA:10015919) Anterior eye structural change, deposit and degeneration(MedDRA:10002693) Corneal structural change, deposit and degeneration(MedDRA:10011049) Corneal perforation(HPO:0100583) Iris and ciliary body structural change, deposit and degeneration(MedDRA:10022952) Corneal perforation(HPO:0100583) Injury, poisoning and procedural complications(MedDRA:10022117) Injuries NEC(MedDRA:10022114) Eye injuries NEC(MedDRA:10027674) Corneal perforation(HPO:0100583) Immune system disorders(MedDRA:10021428) Immune disorders NEC(MedDRA:10027665) Immune and associated conditions NEC(MedDRA:10027682) Corneal perforation(HPO:0100583) |
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Database Frequency: | 4 / 7739 | ||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation | (Orphanet:324530) |
CYSTINOSIS, NEPHROPATHIC | (OMIM:219800) |
Goldberg-Shprintzen megacolon syndrome | (Orphanet:66629) |
Lacrimo-auriculo-dento-digital syndrome | (Orphanet:2363) |