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congenital hereditary endothelial dystrophy type I
Disease Summary
Associated Targets ()
Mondo Description Congenital hereditary endothelial dystrophy I (CHED I) is a rare subtype of posterior corneal dystrophy characterized by a diffuse ground-glass appearance of the corneas and marked corneal thickening from birth or infancy without nystagmus, with blurred vision.
Mondo Term and Equivalent IDs
MONDO:0020365: congenital hereditary endothelial dystrophy type I
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Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
Orphanet:98975
SCTID:416633008
MONDO:0020365
High level summary of knowledge for a disease, including descriptions and datasource references.