Corneal erosion

Symptom Information:

Symptom ID: HPO:0200020
Synonyms:
Corneal ulcer (disorder) [Orphanet:4360]
Perforation of cornea (disorder) [Orphanet:4360]
Corneal erosion (disorder) [Orphanet:4360]
Corneal Perforation [Orphanet:4360]
Corneal Ulcer [Orphanet:4360]
Corneal erosion [Orphanet:4360]
Corneal erosions [OMIM:Corneal erosions]
Corneal ulceration/perforation [Orphanet:4360]
Corneal perforation [Orphanet:4360]
Ulcerative keratitis [Orphanet:4360]
Corneal perforation [MedDRA:10011039]
Perforation corneal [MedDRA:10011039]
Ulcerative keratitis [MedDRA:10064996]
Central corneal ulcer [MedDRA:10064996]
Corneal ulcer marginal [MedDRA:10064996]
Corneal ulcer NEC [MedDRA:10064996]
Corneal ulcer, unspecified [MedDRA:10064996]
Corneal ulceration [MedDRA:10064996]
Mooren's ulcer [MedDRA:10064996]
Necrosis corneal [MedDRA:10064996]
Perforated corneal ulcer [MedDRA:10064996]
Ring corneal ulcer [MedDRA:10064996]
Ulcer corneal [MedDRA:10064996]
Ulcer corneal perforated [MedDRA:10064996]
Corneal ulcer [MedDRA:10064996]
Corneal melt [MedDRA:10064996]
Corneal erosion [MedDRA:10011013]
Corneal erosion multiple [MedDRA:10011013]
Recurrent erosion of cornea [MedDRA:10011013]
Corneal erosions (1 patient) [OMIM:Corneal erosions (1 patient)]
Corneal ulcer [OMIM:Corneal ulcer]
Quality:
Cross references:
HPO:0100583 "Corneal perforation" [Orphanet:4360]
HPO:0000495 "Recurrent corneal erosions" [Orphanet:4360]
Orphanet:4360 "Corneal ulceration/perforation" [Orphanet:4360]
OMIM: "Corneal erosions" [OMIM:Corneal erosions]
OMIM: "Corneal erosions (1 patient)" [OMIM:Corneal erosions (1 patient)]
OMIM: "Corneal ulcer" [OMIM:Corneal ulcer]
UMLS:C0339293 "Corneal Perforation" [Orphanet:4360]
UMLS:C0010043 "Corneal Ulcer" [Orphanet:4360]
UMLS:C0392163 "Corneal erosion" [Orphanet:4360]
Is a (Direct Parents):
Orphanet Abnormality of the eye
HPO         Abnormality of corneal epithelium
MedDRA Eye injuries NEC
MedDRA Immune and associated conditions NEC
MedDRA Corneal structural change, deposit and degeneration
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:
Injury, poisoning and procedural complications(MedDRA:10022117)
    Injuries NEC(MedDRA:10022114)
       Eye injuries NEC(MedDRA:10027674)
          Corneal erosion(HPO:0200020)
Immune system disorders(MedDRA:10021428)
    Immune disorders NEC(MedDRA:10027665)
       Immune and associated conditions NEC(MedDRA:10027682)
          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)
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)