Corneal arcus

Symptom Information:

Symptom ID: HPO:0001084
Synonyms:
Anterior embryotoxon [HPO:0001084]
Arcus lipoidis [HPO:0001084]
Arcus senilis [HPO:0001084]
Corneal annulus [HPO:0001084]
Gerontoxon [HPO:0001084]
Embryotoxon [Orphanet:4460]
Arcus senilis (disorder) [Orphanet:4460]
Embryotoxon (disorder) [Orphanet:4460]
Corneal arcus [OMIM:Corneal arcus]
Quality:
Cross references:
HPO:0000627 "Posterior embryotoxon" [Orphanet:4460]
Orphanet:4460 "Embryotoxon" [Orphanet:4460]
OMIM: "Corneal arcus" [OMIM:Corneal arcus]
UMLS:C0344531 "Embryotoxon" [Orphanet:4460]
Is a (Direct Parents):
Orphanet Abnormality of the eye
HPO         Peripheral opacification 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)
                      Abnormality of corneal stroma(HPO:0011492)
                         Opacification of the corneal stroma(HPO:0007759)
                            Peripheral opacification of the cornea(HPO:0008011)
                               Corneal arcus(HPO:0001084)
                      Corneal opacity(HPO:0007957)
                         Opacification of the corneal stroma(HPO:0007759)
                            Peripheral opacification of the cornea(HPO:0008011)
                               Corneal arcus(HPO:0001084)
MedDRA:
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

Bardet-Biedl syndrome 1 (OMIM:209900 )
CORNEA PLANA 2 (OMIM:217300)
De Barsy syndrome (Orphanet:2962)
HYPERCHOLESTEROLEMIA, AUTOSOMAL DOMINANT, TYPE B (OMIM:144010)
HYPERCHOLESTEROLEMIA, FAMILIAL (OMIM:143890)
HYPERLIPOPROTEINEMIA, TYPE II, AND DEAFNESS (OMIM:144300)
MEGALOCORNEA (OMIM:309300)
MOVED TO 143890 (OMIM:144400)