Corneal scarring
Symptom Information:
Symptom ID: | HPO:0000559 | ||||
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 connective tissue(HPO:0003549) Scarring(HPO:0100699) Corneal scarring(HPO:0000559) 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 opacity(HPO:0007957) Corneal scarring(HPO:0000559) MedDRA: |
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Database Frequency: | 9 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Congenital erythropoietic porphyria | (Orphanet:79277) |
Hereditary sensory and autonomic neuropathy type 4 | (Orphanet:642) |
Hereditary sensory and autonomic neuropathy type 6 | (Orphanet:314381) |
IMMUNODEFICIENCY WITH DEFECTIVE LEUKOCYTE AND LYMPHOCYTE FUNCTIONAND WITH RESPONSE TO HISTAMINE-1 ANTAGONIST | (OMIM:146840) |
KID syndrome | (Orphanet:477) |
Navajo neurohepatopathy | (Orphanet:255229) |
Recessive dystrophic epidermolysis bullosa inversa | (Orphanet:79409) |
Severe generalized recessive dystrophic epidermolysis bullosa | (Orphanet:79408) |
Thiel-Behnke corneal dystrophy | (Orphanet:98960) |