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Human Disease and Mouse Model Detail
Human Disease Oculoectodermal Syndrome; OES
OMIM ID: 600268
Human Phenotype Ontology associations
Synonyms Aplasia Cutis Congenita with Epibulbar Dermoids
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