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Disease Ontology Browser
congenital stromal corneal dystrophy (DOID:0060445)
Alliance: disease page
Synonyms: congenital hereditary stromal dystrophy; CSCD
Alt IDs: OMIM:610048, ICD10CM:H18.5, MESH:C566452, ORDO:101068
Definition: A stromal dystrophy that is characterized by the presence of bilateral corneal opacities that can be seen at or shortly after birth.

Disease References using Mouse Models (1)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
04/09/2024
MGI 6.23 		The Jackson Laboratory