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Disease Ontology Browser
branchiooculofacial syndrome (DOID:0050691)
Alliance: disease page
Alt IDs: OMIM:113620
Definition: A syndrome that is characterized by low birth weight and growth retardation, bilateral branchial clefts.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
MGI 6.21
The Jackson Laboratory