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Human Disease and Mouse Model Detail
Human Disease Corneal Endothelial Dystrophy 1, Autosomal Dominant; CHED1
OMIM ID: 121700
Synonyms Congenital Hereditary Endothelial Dystrophy of Cornea; Corneal Dystrophy, Congenital Hereditary Endothelial; CHED; Corneal Endothelial Dystrophy; Maumenee Corneal Dystrophy
Genes and
mouse models
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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last database update
MGI 6.02
The Jackson Laboratory