Corneal erosion
Symptom Information:
Symptom ID: | HPO:0200020 | |||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) Abnormality of corneal epithelium(HPO:0011495) Corneal erosion(HPO:0200020) MedDRA: Immune system disorders(MedDRA:10021428) Immune disorders NEC(MedDRA:10027665) Immune and associated conditions NEC(MedDRA:10027682) Corneal erosion(HPO:0200020) Injury, poisoning and procedural complications(MedDRA:10022117) Injuries NEC(MedDRA:10022114) Eye injuries NEC(MedDRA:10027674) Corneal erosion(HPO:0200020) Eye disorders(MedDRA:10015919) Anterior eye structural change, deposit and degeneration(MedDRA:10002693) Corneal structural change, deposit and degeneration(MedDRA:10011049) Corneal erosion(HPO:0200020) |
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Database Frequency: | 12 / 7739 | |||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation | (Orphanet:324530) |
Autosomal recessive Alport syndrome | (Orphanet:88919) |
BRESEK syndrome | (Orphanet:85284) |
CORNEAL DYSTROPHY, LATTICE TYPE IIIA | (OMIM:608471) |
CYSTINOSIS, NEPHROPATHIC | (OMIM:219800) |
Congenital sodium diarrhea | (Orphanet:103908) |
Cystinosis | (Orphanet:213) |
Epithelial recurrent erosion dystrophy | (Orphanet:293381) |
Goldberg-Shprintzen megacolon syndrome | (Orphanet:66629) |
Ichthyosis follicularis - alopecia - photophobia | (Orphanet:2273) |
Reis-Bücklers corneal dystrophy | (Orphanet:98961) |
X-linked Alport syndrome | (Orphanet:88917) |