Central corneal dystrophy

Symptom Information:

Symptom ID: HPO:0007881
Synonyms:
Central corneal dystrophy [OMIM:Central corneal dystrophy]
Quality:
Cross references:
OMIM: "Central corneal dystrophy" [OMIM:Central corneal dystrophy]
Is a (Direct Parents):
HPO         Central 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)
                            Central opacification of the cornea(HPO:0011493)
                               Central corneal dystrophy(HPO:0007881)
                      Corneal opacity(HPO:0007957)
                         Opacification of the corneal stroma(HPO:0007759)
                            Central opacification of the cornea(HPO:0011493)
                               Central corneal dystrophy(HPO:0007881)
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Central cloudy dystrophy of Francois (Orphanet:98972)