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Disease Ontology Browser
Schnyder corneal dystrophy (DOID:0060456)
Alliance: disease page
Synonyms: corneal dystrophy crystalline of Schnyder; crystalline stromal dystrophy; hereditary crystalline stromal dystrophy of Schnyder; SCCD; Schnyder crystalline corneal dystrophy
Alt IDs: OMIM:121800, MESH:C535475, ORDO:98967, UMLS_CUI:C0271287
Definition: A stromal dystrophy that is characterized by abnormal deposition of cholesterol and phospholipids in the cornea and that has_material_basis_in heterozygous mutation in the UBAID1 gene on chromosome 1p36.

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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last database update
07/02/2024
MGI 6.13
The Jackson Laboratory