| Human Disease |
Macular Dystrophy, Corneal, 1; MCDC1 OMIM ID: 217800 |
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| Synonyms | Corneal Dystrophy, Macular Type; Groenouw Type II Corneal Dystrophy; MCD | |||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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