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Human Disease and Mouse Model Detail
Human Disease Fryns-Aftimos Syndrome
OMIM ID: 606155
Synonyms Cerebrooculofacial Lymphatic Syndrome; COFL Syndrome; Mental Retardation with Epilepsy and Characteristic Facies; Pachygyria, Mental Retardation, Epilepsy, and Characteristic Facies
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 5.21
The Jackson Laboratory