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Human Disease and Mouse Model Detail
Human Disease

Term: Corneal Endothelial Dystrophy 1, Autosomal Dominant; CHED1
OMIM ID: 121700

Synonyms Congenital Hereditary Endothelial Dystrophy of Cornea; Corneal Dystrophy, Congenital Hereditary Endothelial; CHED; Maumenee Corneal Dystrophy
Associated Genes
 There are currently no human or mouse genes associated with this disease in the MGI database.
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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Send questions and comments to User Support. 		last database update
04/03/2013
MGI 5.12 		The Jackson Laboratory