Recurrent corneal erosions
Symptom Information:
Symptom ID: | HPO:0000495 | |||||||||||||||||||||||||||||||||||||||||||
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) Recurrent corneal erosions(HPO:0000495) MedDRA: Injury, poisoning and procedural complications(MedDRA:10022117) Injuries NEC(MedDRA:10022114) Eye injuries NEC(MedDRA:10027674) Recurrent corneal erosions(HPO:0000495) Eye disorders(MedDRA:10015919) Anterior eye structural change, deposit and degeneration(MedDRA:10002693) Corneal structural change, deposit and degeneration(MedDRA:10011049) Recurrent corneal erosions(HPO:0000495) Immune system disorders(MedDRA:10021428) Immune disorders NEC(MedDRA:10027665) Immune and associated conditions NEC(MedDRA:10027682) Recurrent corneal erosions(HPO:0000495) |
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Database Frequency: | 20 / 7739 | |||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation | (Orphanet:324530) |
BRESEK syndrome | (Orphanet:85284) |
CORNEAL DYSTROPHY, LATTICE TYPE I | (OMIM:122200) |
CYSTINOSIS, NEPHROPATHIC | (OMIM:219800) |
Congenital trigeminal anesthesia | (Orphanet:231013) |
Familial dysautonomia | (Orphanet:1764) |
Goldberg-Shprintzen megacolon syndrome | (Orphanet:66629) |
Hereditary sensory and autonomic neuropathy type 4 | (Orphanet:642) |
IMMUNODEFICIENCY WITH DEFECTIVE LEUKOCYTE AND LYMPHOCYTE FUNCTIONAND WITH RESPONSE TO HISTAMINE-1 ANTAGONIST | (OMIM:146840) |
Ichthyosis follicularis - alopecia - photophobia | (Orphanet:2273) |
Isolated cloverleaf skull syndrome | (Orphanet:2343) |
KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT | (OMIM:148210) |
KID syndrome | (Orphanet:477) |
KLEEBLATTSCHAEDEL | (OMIM:148800) |
Lacrimo-auriculo-dento-digital syndrome | (Orphanet:2363) |
Lattice corneal dystrophy type I | (Orphanet:98964) |
Lymphedema - distichiasis | (Orphanet:33001) |
Macular corneal dystrophy | (Orphanet:98969) |
Microcystic corneal dystrophy | (Orphanet:98956) |
Navajo neurohepatopathy | (Orphanet:255229) |