About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease Macular Dystrophy, Retinal, 1, North Carolina Type; MCDR1
OMIM ID: 136550
Synonyms Central Areolar Pigment Epithelial Dystrophy; CAPED; Foveal Dystrophy, Progressive; Macular Dystrophy; North Carolina Macular Dystrophy; NCMD; Retinal Pigment Epithelial Dystrophy, Central
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
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
12/09/2014
MGI 5.20
The Jackson Laboratory