Congenital corneal dystrophy

Symptom Information:

Symptom ID: HPO:0008005
Synonyms:
Congenital corneal dystrophy [OMIM:Congenital corneal dystrophy]
Quality:
Cross references:
OMIM: "Congenital corneal dystrophy" [OMIM:Congenital corneal dystrophy]
Is a (Direct Parents):
HPO         Corneal dystrophy
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 dystrophy(HPO:0001131)
                         Congenital corneal dystrophy(HPO:0008005)
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

Congenital hereditary endothelial dystrophy type I (Orphanet:98975)
Congenital hereditary endothelial dystrophy type II (Orphanet:293603)
Congenital stromal corneal dystrophy (Orphanet:101068)