Corneal neovascularization
Symptom Information:
Symptom ID: | HPO:0011496 | |||||||||||||||||
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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) Corneal neovascularization(HPO:0011496) MedDRA: Vascular disorders(MedDRA:10047065) Vascular disorders NEC(MedDRA:10047066) Ocular vascular disorders NEC(MedDRA:10030067) Corneal neovascularization(HPO:0011496) |
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Database Frequency: | 7 / 7739 | |||||||||||||||||
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All diseases associated with this symptom:
Corneal intraepithelial dyskeratosis with palmoplantar hyperkeratosis and laryngeal dyskeratosis | (Orphanet:352662) |
Cystinosis | (Orphanet:213) |
Familial vascular leukoencephalopathy | (Orphanet:36383) |
Fish-eye disease | (Orphanet:79292) |
Hereditary mucoepithelial dysplasia | (Orphanet:1839) |
LCAT deficiency | (Orphanet:650) |
Tyrosinemia type 2 | (Orphanet:28378) |