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

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.13
The Jackson Laboratory