Congenital corneal dystrophy
Symptom Information:
Symptom ID: | HPO:0008005 | ||
Synonyms: |
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Cross references: |
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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 dystrophy(HPO:0001131) Congenital corneal dystrophy(HPO:0008005) MedDRA: |
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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) |