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Human Disease and Mouse Model Detail
Human Disease Macular Dystrophy, Retinal, 1, North Carolina Type; MCDR1
OMIM ID: 136550
Human Phenotype Ontology associations
Synonyms Central Areolar Pigment Epithelial Dystrophy; CAPED; Foveal Dystrophy, Progressive, Formerly; 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
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last database update
MGI 6.07
The Jackson Laboratory