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Human Disease and Mouse Model Detail
Human Disease Tukel Syndrome
OMIM ID: 609428
Human Phenotype Ontology associations
Synonyms CFEOM-U; Fibrosis of Extraocular Muscles, Congenital, 4; CFEOM4; Fibrosis of Extraocular Muscles, Congenital, with Ulnar Hand Anomalies
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