Corneal neovascularization

Symptom Information:

Symptom ID: HPO:0011496
Synonyms:
Corneal neovascularisation [HPO:0011496]
Corneal vascularization [HPO:0011496]
Corneal neovascularisation [Orphanet:4340]
Corneal neovascularization (disorder) [Orphanet:4340]
Corneal Neovascularization [Orphanet:4340]
Corneal neovascularization [OMIM:Corneal neovascularization]
Corneal vascularization [OMIM:Corneal vascularization]
Corneal clouding/opacity/vascularisation [Orphanet:4340]
Corneal neovascularisation [MedDRA:10055665]
Corneal neovascularization [MedDRA:10055665]
Corneal neovascularization, unspecified [MedDRA:10055665]
Deep vascularization of cornea [MedDRA:10055665]
Ghost vessels (corneal) [MedDRA:10055665]
Localized vascularization of cornea [MedDRA:10055665]
Pannus (corneal) [MedDRA:10055665]
Deep vascularisation of cornea [MedDRA:10055665]
Localised vascularisation of cornea [MedDRA:10055665]
Quality:
Cross references:
Orphanet:4340 "Corneal clouding/opacity/vascularisation" [Orphanet:4340]
OMIM: "Corneal neovascularization" [OMIM:Corneal neovascularization]
OMIM: "Corneal vascularization" [OMIM:Corneal vascularization]
UMLS:C0085109 "Corneal Neovascularization" [Orphanet:4340]
Is a (Direct Parents):
Orphanet Abnormality of the eye
MedDRA Ocular vascular disorders NEC
Orphanet Opacification of the corneal stroma
HPO         Abnormality of the cornea
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)
Database Frequency: 7 / 7739
Resource:

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)